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Radiation Oncology Journal > Volume 36(3); 2018 > Article
Kim, Jenrow, and Brown: Novel biological strategies to enhance the radiation therapeutic ratio

Abstract

Successful anticancer strategies require a differential response between tumor and normal tissue (i.e., a therapeutic ratio). In fact, improving the effectiveness of a cancer therapeutic is of no clinical value in the absence of a significant increase in the differential response between tumor and normal tissue. Although radiation dose escalation with the use of intensity modulated radiation therapy has permitted the maximum tolerable dose for most locally advanced cancers, improvements in tumor control without damaging normal adjacent tissues are needed. As a means of increasing the therapeutic ratio, several new approaches are under development. Drugs targeting signal transduction pathways in cancer progression and more recently, immunotherapeutics targeting specific immune cell subsets have entered the clinic with promising early results. Radiobiological research is underway to address pressing questions as to the dose per fraction, irradiated tumor volume and time sequence of the drug administration. To exploit these exciting novel strategies, a better understanding is needed of the cellular and molecular pathways responsible for both cancer and normal tissue and organ response, including the role of radiation-induced accelerated senescence. This review will highlight the current understanding of promising biologically targeted therapies to enhance the radiation therapeutic ratio.

Introduction

The concept of a radiation therapeutic ratio for cancer treatment has evolved over the years and generally centers around efforts to maximize the radiation response of cancer cells to achieve local control, while minimizing the potential for radiation-induced acute and late morbidity on normal tissues [1,2]. Both parameters have sigmoidal dose-response curves. Thus, a favorable outcome in dose-response curve is the response of tumor tissue is greater than that of normal tissue to the same dose, meaning that the therapy is effective to tumors, whereas overlapping response of two tissues is highly likely to cause serious consequences to normal tissues and ineffective treatment to tumors. Classically, fractionated radiotherapy (RT) is favored over single large doses, mainly because fractionated RT reduces the potential for late normal tissue toxicity. However, the therapeutic ratio becomes marginal with fractionated RT, especially with large solid tumors. Consequently, three distinct strategies have been evolved to improve its utility. One strategy exploits recent advances in the delivery of radiation using image guided precision localization to permit the delivery of higher doses of radiation to well-defined targets. A second strategy exploits advances in targeting radiation using radiosurgery and/or intensity modulated radiotherapy to minimize exposure and toxicity in the surrounding normal tissues. Both of these strategies are aimed at delivering much higher radiation doses to the tumor tissue, nevertheless the normal tissue and organ tolerance remains the limiting factor. A third strategy involves the application of recent cellular and molecular findings to pharmacologically prevent/decrease normal tissue toxicity or enhance the intrinsic radiosensitivity of tumor tissue. This review highlights pre-clinical and early clinical data derived from the biological targeted cancer therapies that are translatable for future clinical trials.

Targeted Cancer Therapy and Radiotherapy

The interaction between targeted therapies and RT is of clinical importance for at least two reasons. Targeted cancer therapies are often combined with conventional approaches such as RT, so the effect of targeted therapies on radiation effectiveness and vice-versa is important. Additionally, targeted therapies act on specific molecular targets that are associated with cancer, whereas radiation (and most standard chemotherapies) acts on all rapidly dividing normal and cancerous cells. Consequently, the effects of targeted therapies are often cytostatic, whereas radiation (and conventional chemotherapy agents) generally kill rapidly dividing cancer cells. Specific inhibitors have been developed targeting the signal transduction pathways. Among them, three pathways are of particular interest when combined with radiation. The PI3K/mTOR pathway has been extensively studied in conjunction with radiation [3,4]. Relatedly, the metabolic state of cancers and targeted metabolic reprogramming critically affect radiotherapy effectiveness [5]. Another pathway of interest in the cancer radiobiology is DNA damage response and checkpoint regulators of the cell cycle [6].

1. PI3K/mTOR and radiotherapy

The PI3K/AKT/mTOR pathway is an intracellular signaling pathway important in regulating the cell cycle. It is directly related to cellular quiescence, proliferation, cancer, and longevity. The protein complex mTORC1 is a convergence point for multiple signaling pathways that control cell growth and proliferation. mTOR is a nutrient-sensing enzyme that regulates cell growth in nearly all eukaryotic species. Since the PI3K/mTOR pathway is frequently activated or dysregulated in many tumors, several classes of agents targeting this pathway are in under clinical development (Fig. 1). Currently, rapamycin analogs (rapalogs) are in clinical use as single or combination agents (e.g., renal, breast, pancreatic, gastrointestinal and lung cancers).
Since PI3K/mTOR pathways are altered in many human cancers and the increased activation of these signaling pathways have been implicated in the tumor radioresistance, numerous studies have been carried out to determine the extent of radiation modification using in vitro and in vivo cancer models. Early studies showed enhanced radiation damage of tumor vasculature when radiation was combined with mTOR inhibitor (e.g., everolimus) in an in vivo mouse tumor model but no in vitro radiosensitization of cancer cells grown in cell culture, hence, it was concluded that mTOR inhibitors exert their enhanced radiation response by inhibiting angiogenesis [7,8]. Subsequent reports have shown that mTOR inhibitors enhance the radiation response of tumor cells both in vitro and in vivo regardless of the timing and schedule of mTOR inhibition [9-12]. More recently, Hayman et al. [13,14] further showed that the inhibition of mTOR reduces eIF4E, a key factor in the translation which initiates the formation of the eIF4F cap complex required for cap-dependent translation. Elevated eIF4E is also correlated with both chemo and radioresistance and selectively silencing eIF4E was shown to enhance the radiosensitivity of cancer cell lines but not normal cells.
At the cellular level, other investigators showed that mTOR inhibitors (e.g., temsirolimus) could overcome the radioresistance of hypoxic tumors, since the upregulation of mTOR regulates the hypoxia-inducible factor-1α (HIF-1α) pathway [15]. Indeed, mTOR inhibition reduces oxygen consumption through inhibition of the mitochondrial respiratory complex I [16]. Our own data show that increased radiosensitivity of tumor cells is in part related to increased ROS production through a feedback loop involving AKT suppression and upregulation of AMPK (manuscript in preparation).
What is clear is that the mechanisms by which mTOR inhibitor enhances tumor radiosensitivity are multi-factorial. Currently, several clinical phase II studies are underway in which everolimus is administered in combination with radiation therapy for the treatment of lung and brain tumors.

2. Metabolic reprogramming and radiotherapy

In recent years, metformin, an oral anti-diabetic biguanide medication for type II diabetes, has attracted interest as a cancer therapeutics. The widespread use of metformin as an anti-diabetic drug, its expected safety profile, and encouraging pre-clinical data led to the several clinical trials evaluating the anti-cancer properties of metformin in combination with chemotherapeutic drugs and fractionated radiotherapy.
Though metformin has been in use for decades to reduce blood sugar levels, the exact mechanisms by which it exerts this anti-diabetic effect is not completely understood. It is widely accepted that metformin decreases hepatic gluconeogenesis and lowers insulin levels, with strong experimental evidence suggesting that it decreases ATP production by acting on mitochondrial respiratory complex I, ultimately activating AMP kinase with secondary inhibition of protein synthesis [17]. This pathway is known to affect the downstream PTEN/PI3K/AKT/mTOR system which plays a pivotal role in cancer’s unregulated growth (Fig. 1).
Mechanistic studies to date have demonstrated that metformin enhances the therapeutic gain of RT in multiple ways. Some researchers [18,19] have shown that metformin enhances the radiosensitivity of MCF-7 human breast cancer cells and lung cancer cells in both in vitro and in vivo models. They further showed that radiation and metformin together activate AMPK leading to inactivation of mTOR and suppression of its downstream effectors such as S6K1 and 4EBP1. Suppression of the 4EBP1 protein reduces eIF4E, enhances the radiosensitivity of several human cancer cells (see section in PI3K/mTOR and Radiotherapy). Others suggest that metformin reduces tumor hypoxia, presumably through the inhibition of mTOR pathway and that it may be beneficial if administered prior to single large dose of radiation [20]. In addition to its inhibition of HIF-1α via the mTOR pathway, metformin is an inhibitor of complex I in the mitochondrial respiratory chain so that the utilization of molecular oxygen is reduced, thereby making the excess oxygen available to the tumor microenvironment.
Data suggest that the mechanism of radiosensitization by metformin may derive not only from re-oxygenation of the hypoxic tumor but from other cellular mechanism as well, especially when metformin is combined with high dose per fraction (more than 8–10 Gy per fraction) radiation. High doses of irradiation is known to shut down the tumor vasculature and the subsequent radiation-induced hypoxia and low glucose would preferentially favor tumor necrosis [21]. These data provide a pre-clinical rationale of combining radiosurgery and single high dose metformin in the clinical settings. Currently, a randomized phase II trial of concurrent chemoradiotherapy +/- metformin in locally advanced NSCLC is underway [22].
Arsenic trioxide (ATO) is a US Food and Drug Administration approved anti-tumor drug (e.g., acute promyelocytic leukemia), that inhibits the mitochondrial complex III activity in the electron transport chain. Similar to results with combined metformin and radiation, a strong synergistic action of ATO has been shown when the radiation is delivered shortly after the drug administration. Mitochondrial inhibitors such as metformin or ATO, have a marginal cytotoxic effect when administered alone, whereas combining with these inhibitors with radiation has a dramatic cytotoxic effect [23,24].

3. Cell cycle checkpoint inhibitors and radiotherapy

The integrity of DNA replication and repair during cell proliferation is normally tightly controlled by several key cell cycle checkpoint proteins, including cyclin-dependent kinase (CDK), checkpoint kinase, and WEE1 kinase (WEE1). It is well known that ionizing radiation induces both doubleand single-strand DNA breaks which disrupt cell proliferation. These aberrant DNA structures induce signaling pathways involved in the DNA damage response (DDR), which regulate these cell cycle checkpoints and DNA repair. Two key kinases involved in this response are ataxia telangiectasia-mutated (ATM), activated primarily by DNA double-strand breaks, and ATM- and Rad3-related (ATR), activated by a broad spectrum of DNA lesions. ATM and ATR work in a coordinated fashion to effect homologous recombination (HR) repair, involving a gradual switch from ATM to ATR activation [25]. This is facilitated by two specific substrates of ATM and ATR, CHK2 and CHK1, respectively. Activation of the G1/S checkpoint by DNA double-strand breaks is regulated by p53, which is a direct substrate of ATM/ATR, as well as CHK1 and CHK2 [26-28]. Activation of the G2/M checkpoint by DNA double-strand breaks is more selectively regulated by the ATR-CHK1 [29,30].
Several inhibitors of CHK1 and CHK2 are being investigated as radiosensitizers, both in pre-clinical and clinical settings. The DDR in tumor cells differs significantly from that in normal cells, with tumor cells often having defective DNA damage signaling through loss of ATM or p53 mutations. Since p53 mutations compromise efficient G1 checkpoint signaling, the DDR in tumor cells carrying these mutations depends more heavily on the ATR-CHK1-activated G2/M checkpoint for cell cycle arrest. Thus, checkpoint inhibitors selectively targeting the ATR-CHK1 pathway have the potential to sensitize tumor cells to radiation-induced DNA damage without sensitizing normal cells with wild type p53. Such compounds are also being investigated in this context and appear to be potent and selective radiosensitizers of cancer cells [31,32].
CHK1 functions in HR repair, stabilizing replication forks, and inhibiting apoptosis. Many CHK1 inhibitors exhibit radiosensitization in clinical models [33,34]. For example, MK-8776, a potent and selective ATP-competitive CHK1 inhibitor that increases cell sensitivity to DNA-damaging agents, is undergoing phase II clinical trials with cytotoxic chemotherapy (e.g., gemcitabine, cytarabine, etc.). VE-821, a potent ATR inhibitor, has been shown to enhance the radiosensitivity of pancreatic cancer cells both in vitro and in vivo [35]. As expected, this inhibitor decreased HR repair. Both CHK1 and ATR inhibitors exhibit their radiation enhancement regardless of the mutational status of p53, which is consistent with the loss of checkpoint control at both the G1/S and G2/M checkpoints as well as compromised HR repair.
Many human tumors exhibit overexpression of WEE1, which selectively regulates the G2/M checkpoint in response to DNA damage by inhibiting CDK1. Pre-clinical studies have shown that WEE1 also participates in DNA repair by stabilizing DNA replication forks. WEE1 inhibitors, therefore, have the potential to remove the G2/M block and to compromise WEE1-mediated DNA repair. MK-1775, a selective, small molecule inhibitor of WEE1, has been shown to radiosensitize multiple human cancer cell lines [36] and is currently being investigated in a clinical trial in conjunction with fractionated RT in patients with glioblastoma multiforme [37]. Radiation enhancement by WEE1 inhibitors is dependent on the p53 status in cell culture studies, where mutated p53 cells are preferentially radiosensitized whereas wild type p53 cells show no significant radiation enhancement [38]. Cells in G2 phase are preferentially sensitized by WEE1 inhibitors, reflecting the loss of WEE1-mediated DNA repair.

Immune Modulators and Radiotherapy

Ever since the early 1960s, when presence of tumor specific antigens was convincingly demonstrated [39,40], many attempts have been made to exploit the power of host immunity against these tumor antigens. Successful clinical results have been elusive. Only within the past 7 years, with the advent and success of immune check point inhibitors as a treatment for advanced metastatic cancers, has immunotherapy moved to the center stage of clinical oncology [41-44]. Further, excitement was generated when local radiotherapy was combined with check point inhibitors and widespread metastatic tumor clearance was achieved [45-47]. In the past 2 years, numerous clinical trials have been initiated combining either fractionated radiotherapy or stereotactic hypofractionated radiotherapy with check point inhibitors [48,49]. Pre-clinical immuno-radiobiology research is underway to address some key pressing questions related to the optimization of radiation dose, timing, and fractionation schedules of RT for combination therapy with these inhibitors [49,50].

1. Immune check point inhibitor and radiotherapy

CTLA4 is a CD28 homolog that acts the early stages of immune response by affecting the interaction between T cells and antigen-presenting cells in the lymph nodes. PD-1/PDL1 suppress T cells later on during the effector phase of the immune response, especially in the periphery. Anti-CTLA4 therapies increase T cell activation by enhancing proliferation and reducing Treg immunosuppression. On the other hand, anti-PD-1/PD-L1 therapies act to restore T cells that are exhausted due to chronic exposure to carcinogen and the accumulation of mutations over time [44]. There are several new classes of agents that are able to inhibit immune check points. Check point inhibitors targeting CTLA4 (ipilimumab), PD-1 (nivolumab, pembrolizumab) and PD-L1 (atezolizumab and durvalumab) have been developed with demonstrated efficacy in unresectable or metastatic refractory melanoma, and advanced squamous and non-small cell lung cancers and are being developed for many other tumors as well (Fig. 2).
Like many other therapeutic regimen used in combination with RT (e.g., cytotoxic chemotherapy, targeted therapy), key radiobiological parameters play important roles when combined with immune checkpoint inhibitors [51]. Clinical and pre-clinical studies are underway to address some unknowns such as the effect of radiation dose per fraction, irradiated tumor volume and time sequence of the drug administration. Hypofractionation with 8 Gy appears to be more effective than lower dose per fraction irradiation in generating so called ‘abscopal’ effect (24 Gy in 3 fractions yielded a larger effect than 30 Gy in 5 fractions) [48]. In the pre-clinical setting, abscopal effects have been reported using these dose regimens in combination with CTLA4 blockade [48]. The other factor is the timing and sequence of the inhibitor administration relative to RT. At present, administration of the inhibitor prior to RT is preferred because the high single dose of hypofractionated RT may destroy tumor vasculature thereby preventing the cytotoxic T cell from reaching the core of large solid tumors. However the optimum timing remains an area of investigation since lymphocytes are among the most radiosensitive cells of body and the damaging effects of prior radiation on a subsequent immunological event based on T lymphocytes needs to be better understood. Although the combined effects of RT and immune checkpoint inhibitor on the abscopal response is exciting, it is still considered a rare event [49]. Many other immune suppressive factors in the tumor microenvironment are in play in addition to the immune checkpoints [50].

2. Immune suppressors and radiotherapy

The tumor microenvironment harbors several immune suppressors such as myeloid derived macrophages, regulatory T cells, and TGFβ, to name a few [51]. The local tumor microenvironment is usually characterized as being acidic, having low oxygen and deprived of micronutrients. These conditions favor attracting myeloid derived macrophages and activating them to so-called M2 type macrophages, also known as tumor associated macrophage (TAM). TAMs are anti-inflammatory and immune-regulatory, and are therefore tumor promoting, whereas activated M1 type macrophages are pro-inflammatory and tumoricidal. TAM infiltrations have been shown to have a negative prognostic relevance for most tumor types [52]. Thus several attempts have been made to target these cells. Among them, the colony stimulating factor 1 receptor (CSF1-R) axis has gained the most attention and a CSF1-R inhibitor is undergoing a clinical trial as a monotherapy [53]. Since activated macrophages play a significant role in the pathogenesis of radiation induced normal tissue damage, we and others have studied the effect of suppressing macrophage mediated pro-inflammatory cytokines on the normal tissue injury (e.g., skin and CNS). Suppression of pan-cytokines have significantly mitigated the radiation induced skin damage and cognitive dysfunction in the brain [54,55]. Recently, Acharya et al. [56] have published results of a similar abrogation of the radiation induced cognitive dysfunction by depleting activated microglia using a CSF1-R inhibitor.
In this context, it would be highly desirable to determine whether the depletion of TAM with CSF1-R inhibitor would enhance the tumor radiation response or not. If it shows an enhancing effect, this approach would be another novel strategy for enhancing the therapeutic ratio. Furthermore, a combination with immune checkpoint inhibitors and the depletion of TAM with CSF1-R inhibitors would be a potentially exciting new approach.
TGFβ is a multifunctional and pleiotropic cytokine affecting many cellular processes including epithelial cell growth, mesenchymal cell proliferation, and extracellular matrix production. Irradiation, even at low doses, is one of the few exogenous factors known to induce TGFβ activation and TGFβ is believed to play a central role in mediating radiationinduced anti-tumor immunity [57] and tissue fibrosis (skin, lung) [58,59]. In advanced cancers, TGFβ promotes tumor growth and metastasis [60]. Using an anti-TGFβ monoclonal antibody, phase I clinical trials were carried out in patients with advanced malignant melanoma and renal cell carcinoma [61]. A pre-clinical study was also carried out with combining radiotherapy with an anti-TGFβ agent. Radiosensitivity of tumor cells were enhanced both in vitro and in vivo [62]. Recently, a phase I clinical study was conducted in metastatic breast cancer patients using a TGFβ blockade and focal hypofractionated RT administered to the metastatic foci. The data suggest that the combined approach induces an abscopal response in a few patients [63]. Blocking an immunosuppressive cytokine alone with local RT may not be sufficient, but multi-pronged approach such as immune check point inhibitors and activated M2 macrophage depletion need to be studied further, because they may prove to be a successful approach.
The use of immunosupressive approaches other than M2 macrophages, such as myeloid-derived-suppressor cells, MDSC, is worth considering since these immunosuppressive myeloidderived cells also infiltrate tumors after RT. For example, STING-dependent MDSC infiltrate tumors after radiation exposure providing an immunosuppressive environment and their blockade enhances the effectiveness of RT [64]. Regulatory T-cell depletion has also been shown to enhance RT efficacy in pre-clinical lung and colon cancer models [65].

Strategies to Prevent/Mitigate/Treat the Normal Tissue Injury

Recent advances in our understanding of the cellular and molecular pathways leading to tissue and organ damage have provided a novel insight into the mechanisms of pathogenesis. Strategies aimed at reducing or counteracting oxidative stress and the resulting excessive production of reactive oxygen and nitrogen chemical species (ROS and RNS, respectively) and pro-inflammatory cytokines have been covered in detail in this journal [66]. In this section, we will briefly review new emerging strategies involving interference of the pathogenic cell signaling pathways and role of radiation-induced senescence.

1. Inhibition of mTOR and HIF pathway

We have discussed the role of rapamycin and its analogs as a radiosensitizer in the foregoing section on the PI3K/mTOR pathway. The radiosensitizing effect was shown in mostly tumor tissues. Interestingly, similar inhibitors have been shown to protect or mitigate the radiation induced normal tissue injury [67,68]. The underlying mechanisms for these mitigating effect are not well understood, but experimental correlative data suggest that the mitigation may be mediated through anti-apoptosis, anti-senescence and less γ-H2AX, etc. It is interesting to note that rapamycin slows aging and extends life span in a variety of species from worm to mammals. In this context, metformin, another radiosensitizer, included in our previous discussion, demonstrates radioprotection in some normal tissues, presumably through AMPK upregulation leading to mTOR inhibition (Fig. 1).
Inhibition of the HIF-1α pathway has been shown to mitigate radiation-induced gastrointestinal toxicity [69,70]. Using a small molecule inhibitor of prolyl hydroxylases, the acute gastrointestinal toxicities following high dose of irradiation of the abdomen significantly mitigated its acute and late toxicity. The inhibitor increases HIF-2 expression, improves epithelial integrity, reduces apoptosis and increases intestinal angiogenesis [69]. Interestingly, the inhibitor did not mitigate against the bone marrow syndrome following total body irradiation.

2. Role of senolytics

Cellular senescence, which is a normal consequence of aging, can result from DNA damage such as that found after radiation exposure as well as oxidative stress, and chronic inflammation. Senescent cells lose the proliferative potential normally found in replication-competent cells and becomes resistant to apoptosis, with an increase in metabolic activity. These changes are often accompanied by the development of a phenomenon known as senescence-associated secretory phenotype (SASP) (Fig. 3). The SASP entails release of proinflammatory cytokines and chemokines, tissue-damaging proteases, factors that can affect stem and progenitor cell function, homeostatic factors, and growth factors, among others. Hence, senescent cells that express the SASP can have substantial local and systemic pathogenic effects.
Laboratory studies have confirmed the importance of senescence as a cause of radiation toxicity in bone marrow, skin and lung and of toxicity from DNA damaging chemotherapy [1,71-74]. Indeed, a recent study in the radiation biology literature showed that radiation-induced lung fibrosis in mice was reversed completely following treatment with ABT-263, a known senolytic drug targeting Bcl2/xL [75]. Both epithelial cell and endothelial cell populations have been implicated [76]. Using another senolytic (e.g., HSP-90 inhibitor), a significant mitigation of radiation-induced skin injury was found in mice, especially late injury endpoints such as leg contraction and fibrosis [77].
Multiple pharmacological strategies are under investigation to remove senescent cells from non-genetically modified animals, using so-called ‘senolytic agents’, including small molecules, peptides, and antibodies with varying degrees of success [78,79]. Some senolytic agents are cell and tissue specific; others are not. Several pathways have been identified including the Bcl-2 family, PI3K/mTOR, tyrosine kinase receptors, and HSP-90, to name a few. It is interesting to note that the most senolytic drugs were initially being developed as anti-cancer agents, since some of the signaling pathways in tumor and senescent cells overlap each other. In the near future, more pre-clinical radiobiological studies are needed to determine the role of senolytics as either mitigators or therapeutics in normal tissue and organ injury but also therapeutics to enhance tumor response.

Conclusion

Recent advances in the cellular and molecular pathways of tumor growth and the pathogenesis of tissue and organ injury provide novel strategies to enhance the radiation therapeutic ratio. Radiobiological research is aimed to optimize combined therapeutic regimens of radiation and targeted therapies and immunotherapeutics. Efforts to minimize or mitigate the risk of radiation injury constitute a promising direction of future study.

Notes

Conflict of Interest

No potential conflict of interest relevant to this article are reported.

Acknowledgments

The studies were support in part by the National Institutes of Health under awards: No. U19-A1067734 (PI: John Moulder, Medical College of Wisconsin; Program Director Jae Ho Kim, Mitigating and treating radiation-induced CNS injury); No. R-21-CA205660 (PI: Jae Ho Kim, Improving the radiation therapeutic ratio by inhibiting pro-inflammatory cytokines), and No. RO1-CA218596 (PI: James Ewing and Stephen Brown, MRI Signatures of response to high-dose radiotherapy in rat models of cerebral tumor). We thank Andrew Kolozsvary and Karen Lapanowski, our long time collaborators for expert technical assistance.

Fig. 1.
The abbreviated signaling pathways regulating mTORC1. The protein complex mTORC1 is a convergence point for multiple signaling pathways that control cell growth and proliferation. Rapamycin and its analogs inhibit mTOR. Metformin activates AMPK, which in turn inhibits mTOR. Activated mTOR increases eIF4E through eIF4G complex. Increased eIF4E is correlated to the radioresistance.
roj-2018-00332f1.jpg
Fig. 2.
Diagram illustrating where immune check point inhibitors block specific check point proteins. Ipilimumab inhibits CTLA4 (cytotoxic T-lymphocyte associated protein 4). Nivolumab and pembrolizumab inhibit PD-1 (programmed death protein). Atezolizumab and durvalumab inhibit PD-L1 (programmed death ligand).
roj-2018-00332f2.jpg
Fig. 3.
Radiation induces accelerated senescence. Depending on the dose of radiation, normal tissues sustain sub-lethal damage, unable to divide but metabolically active. Senescent cells elaborate a complex mixture of cytokines and chemokines known as the senescence-associated secretory phenotype, SASP. This in turn would be source of increased, sustained source of ROS, chronic inflammation and modify immune phenotypes and stimulate fibrotic tissue remodeling. Ultimately, the presence of senescent cells impede the recovery and repair of remaining irradiated normal tissues and organs. ROS, reactive oxygen species; RNS, reactive nitrogen species.
roj-2018-00332f3.jpg

References

1. Citrin DE. Recent Developments in Radiotherapy. N Engl J Med 2017;377:1065–75.
crossref pmid
2. Giaccia AJ. Molecular radiobiology: the state of the art. J Clin Oncol 2014;32:2871–8.
crossref pmid pmc
3. Kim KW, Myers CJ, Jung DK, Lu B. NVP-BEZ-235 enhances radiosensitization via blockade of the PI3K/mTOR pathway in cisplatin-resistant non-small cell lung carcinoma. Genes Cancer 2014;5:293–302.
pmid pmc
4. Chang L, Graham PH, Hao J, et al. Emerging roles of radioresistance in prostate cancer metastasis and radiation therapy. Cancer Metastasis Rev 2014;33:469–96.
crossref pmid
5. Tang L, Wei F, Wu Y, et al. Role of metabolism in cancer cell radioresistance and radiosensitization methods. J Exp Clin Cancer Res. 2018;37:87.
crossref pmid pmc pdf
6. Jaklevic B, Uyetake L, Lemstra W, et al. Contribution of growth and cell cycle checkpoints to radiation survival in Drosophila. Genetics 2006;174:1963–72.
crossref pmid pmc
7. Eshleman JS, Carlson BL, Mladek AC, Kastner BD, Shide KL, Sarkaria JN. Inhibition of the mammalian target of rapamycin sensitizes U87 xenografts to fractionated radiation therapy. Cancer Res 2002;62:7291–7.
pmid
8. Shinohara ET, Cao C, Niermann K, et al. Enhanced radiation damage of tumor vasculature by mTOR inhibitors. Oncogene 2005;24:5414–22.
crossref pmid pdf
9. Albert JM, Kim KW, Cao C, Lu B. Targeting the Akt/mammalian target of rapamycin pathway for radiosensitization of breast cancer. Mol Cancer Ther 2006;5:1183–9.
crossref pmid
10. Nagata Y, Takahashi A, Ohnishi K, et al. Effect of rapamycin, an mTOR inhibitor, on radiation sensitivity of lung cancer cells having different p53 gene status. Int J Oncol 2010;37:1001–10.
crossref pmid
11. Mauceri HJ, Sutton HG, Darga TE, et al. Everolimus exhibits efficacy as a radiosensitizer in a model of non-small cell lung cancer. Oncol Rep 2012;27:1625–9.
crossref pmid
12. Nassim R, Mansure JJ, Chevalier S, Cury F, Kassouf W. Combining mTOR inhibition with radiation improves antitumor activity in bladder cancer cells in vitro and in vivo: a novel strategy for treatment. PLoS One 2013;8:e65257.
crossref pmid pmc
13. Hayman TJ, Williams ES, Jamal M, Shankavaram UT, Camphausen K, Tofilon PJ. Translation initiation factor eIF4E is a target for tumor cell radiosensitization. Cancer Res 2012;72:2362–72.
crossref pmid
14. Hayman TJ, Wahba A, Rath BH, et al. The ATP-competitive mTOR inhibitor INK128 enhances in vitro and in vivo radiosensitivity of pancreatic carcinoma cells. Clin Cancer Res 2014;20:110–9.
crossref pmid
15. Ushijima H, Suzuki Y, Oike T, et al. Radio-sensitization effect of an mTOR inhibitor, temsirolimus, on lung adenocarcinoma A549 cells under normoxic and hypoxic conditions. J Radiat Res 2015;56:663–8.
crossref pmid pmc pdf
16. Kelly CJ, Hussien K, Fokas E, et al. Regulation of O2 consumption by the PI3K and mTOR pathways contributes to tumor hypoxia. Radiother Oncol 2014;111:72–80.
crossref pmid pmc
17. Kalender A, Selvaraj A, Kim SY, et al. Metformin, independent of AMPK, inhibits mTORC1 in a rag GTPase-dependent manner. Cell Metab 2010;11:390–401.
crossref pmid pmc
18. Song CW, Lee H, Dings RP, et al. Metformin kills and radiosensitizes cancer cells and preferentially kills cancer stem cells. Sci Rep 2012;2:362.
crossref pmid pmc pdf
19. Storozhuk Y, Hopmans SN, Sanli T, et al. Metformin inhibits growth and enhances radiation response of non-small cell lung cancer (NSCLC) through ATM and AMPK. Br J Cancer 2013;108:2021–32.
crossref pmid pmc pdf
20. Zannella VE, Dal Pra A, Muaddi H, et al. Reprogramming metabolism with metformin improves tumor oxygenation and radiotherapy response. Clin Cancer Res 2013;19:6741–50.
crossref pmid
21. Brown SL, Nagaraja TN, Aryal MP, et al. MRI-tracked tumor vasculature changes in the hours after single fraction irradiation. Radiat Res 2015;183:713–21.
crossref pmid
22. NRG Oncology. Randomized phase II trial of concurrent chemoradiotherapy +/- metformin HCL in locally advanced NSCLC (NRG-LU001, ClinicalTrials.gov NCT02186847) Philadelphia, PA: NRG Oncology; 2016.

23. Lew YS, Kolozsvary A, Brown SL, Kim JH. Synergistic interaction with arsenic trioxide and fractionated radiation in locally advanced murine tumor. Cancer Res 2002;62:4202–5.
pmid
24. Kim JH, Lew YS, Kolozsvary A, Ryu S, Brown SL. Arsenic trioxide enhances radiation response of 9L glioma in the rat brain. Radiat Res 2003;160:662–6.
crossref pmid
25. Shiotani B, Zou L. Single-stranded DNA orchestrates an ATMto-ATR switch at DNA breaks. Mol Cell 2009;33:547–58.
crossref pmid pmc
26. Khosravi R, Maya R, Gottlieb T, Oren M, Shiloh Y, Shkedy D. Rapid ATM-dependent phosphorylation of MDM2 precedes p53 accumulation in response to DNA damage. Proc Natl Acad Sci U S A 1999;96:14973–7.
crossref pmid pmc
27. Origanti S, Cai SR, Munir AZ, White LS, Piwnica-Worms H. Synthetic lethality of Chk1 inhibition combined with p53 and/or p21 loss during a DNA damage response in normal and tumor cells. Oncogene 2013;32:577–88.
crossref pmid pdf
28. Bartek J, Lukas J. Chk1 and Chk2 kinases in checkpoint control and cancer. Cancer Cell 2003;3:421–9.
crossref pmid
29. Sorensen CS, Hansen LT, Dziegielewski J, et al. The cellcycle checkpoint kinase Chk1 is required for mammalian homologous recombination repair. Nat Cell Biol 2005;7:195–201.
crossref pmid pdf
30. Tao Y, Leteur C, Yang C, et al. Radiosensitization by Chir-124, a selective CHK1 inhibitor: effects of p53 and cell cycle checkpoints. Cell Cycle 2009;8:1196–205.
crossref pmid
31. Engelke CG, Parsels LA, Qian Y, et al. Sensitization of pancreatic cancer to chemoradiation by the Chk1 inhibitor MK8776. Clin Cancer Res 2013;19:4412–21.
crossref pmid pmc
32. Suzuki M, Yamamori T, Bo T, Sakai Y, Inanami O. MK-8776, a novel Chk1 inhibitor, exhibits an improved radiosensitizing effect compared to UCN-01 by exacerbating radiation-induced aberrant mitosis. Transl Oncol 2017;10:491–500.
crossref pmid pmc
33. Qiu Z, Oleinick NL, Zhang J. ATR/CHK1 inhibitors and cancer therapy. Radiother Oncol 2018;126:450–64.
crossref pmid
34. Morgan MA, Parsels LA, Maybaum J, Lawrence TS. Improving the efficacy of chemoradiation with targeted agents. Cancer Discov 2014;4:280–91.
crossref pmid pmc
35. Prevo R, Fokas E, Reaper PM, et al. The novel ATR inhibitor VE-821 increases sensitivity of pancreatic cancer cells to radiation and chemotherapy. Cancer Biol Ther 2012;13:1072–81.
crossref pmid pmc
36. Hirai H, Iwasawa Y, Okada M, et al. Small-molecule inhibition of Wee1 kinase by MK-1775 selectively sensitizes p53-deficient tumor cells to DNA-damaging agents. Mol Cancer Ther 2009;8:2992–3000.
crossref pmid
37. Sarcar B, Kahali S, Prabhu AH, et al. Targeting radiationinduced G(2) checkpoint activation with the Wee-1 inhibitor MK-1775 in glioblastoma cell lines. Mol Cancer Ther 2011;10:2405–14.
crossref pmid pmc
38. Bridges KA, Hirai H, Buser CA, et al. MK-1775, a novel Wee1 kinase inhibitor, radiosensitizes p53-defective human tumor cells. Clin Cancer Res 2011;17:5638–48.
crossref pmid pmc
39. Old LJ, Boyse EA. Immunology of experimental tumors. Annu Rev Med 1964;15:167–86.
crossref pmid
40. Old LJ, Stockert E, Boyse EA, Kim JH. Antigenic modulation: loss of TL antigen from cells exposed to TL antibody. Study of the phenomenon in vitro. J Exp Med 1968;127:523–39.
crossref pmid pmc
41. Callahan MK, Wolchok JD, Allison JP. Anti-CTLA-4 antibody therapy: immune monitoring during clinical development of a novel immunotherapy. Semin Oncol 2010;37:473–84.
crossref pmid pmc
42. Pardoll DM. The blockade of immune checkpoints in cancer immunotherapy. Nat Rev Cancer 2012;12:252–64.
crossref pmid pmc pdf
43. Brahmer JR, Pardoll DM. Immune checkpoint inhibitors: making immunotherapy a reality for the treatment of lung cancer. Cancer Immunol Res 2013;1:85–91.
crossref pmid pmc
44. Rizvi NA, Hellmann MD, Snyder A, et al. Cancer immunology: mutational landscape determines sensitivity to PD-1 blockade in non-small cell lung cancer. Science 2015;348:124–8.
crossref pmid pmc
45. Postow MA, Callahan MK, Barker CA, et al. Immunologic correlates of the abscopal effect in a patient with melanoma. N Engl J Med 2012;366:925–31.
crossref pmid pmc
46. Golden EB, Demaria S, Schiff PB, Chachoua A, Formenti SC. An abscopal response to radiation and ipilimumab in a patient with metastatic non-small cell lung cancer. Cancer Immunol Res 2013;1:365–72.
crossref pmid pmc
47. Formenti SC, Demaria S. Systemic effects of local radiotherapy. Lancet Oncol 2009;10:718–26.
crossref pmid pmc
48. Dewan MZ, Galloway AE, Kawashima N, et al. Fractionated but not single-dose radiotherapy induces an immune-mediated abscopal effect when combined with anti-CTLA-4 antibody. Clin Cancer Res 2009;15:5379–88.
crossref pmid pmc
49. Schaue D, Ratikan JA, Iwamoto KS, McBride WH. Maximizing tumor immunity with fractionated radiation. Int J Radiat Oncol Biol Phys 2012;83:1306–10.
crossref pmid
50. McBride WH, Ganapathy E, Lee MH, Nesseler JP, Nguyen C, Schaue D. A perspective on the impact of radiation therapy on the immune rheostat. Br J Radiol 2017;90:20170272.
crossref pmid pmc
51. Koo T, Kim IA. Radiotherapy and immune checkpoint blockades: a snapshot in 2016. Radiat Oncol J 2016;34:250–9.
crossref pmid pmc pdf
52. Qian BZ, Pollard JW. Macrophage diversity enhances tumor progression and metastasis. Cell 2010;141:39–51.
crossref pmid pmc
53. Cannarile MA, Weisser M, Jacob W, Jegg AM, Ries CH, Ruttinger D. Colony-stimulating factor 1 receptor (CSF1R) inhibitors in cancer therapy. J Immunother Cancer 2017;5:53.
crossref pmid pmc pdf
54. Jenrow KA, Brown SL, Lapanowski K, Naei H, Kolozsvary A, Kim JH. Selective inhibition of microglia-mediated neuroinflammation mitigates radiation-induced cognitive impairment. Radiat Res 2013;179:549–56.
crossref pmid pmc
55. Jenrow KA, Brown SL, Kolozsvary AJ, Lapanowski K, Kim JH. Time-dependent inhibition of pan-inflammatory cytokines mitigates radiation-induced skin injury in mice. Radiat Res 2014;182:316–21.
crossref pmid
56. Acharya MM, Green KN, Allen BD, et al. Elimination of microglia improves cognitive function following cranial irradiation. Sci Rep 2016;6:31545.
crossref pmid pmc pdf
57. Vanpouille-Box C, Diamond JM, Pilones KA, et al. TGFβ is a master regulator of radiation therapy-induced antitumor immunity. Cancer Res 2015;75:2232–42.
crossref pmid pmc
58. Ehrhart EJ, Segarini P, Tsang ML, Carroll AG, Barcellos-Hoff MH. Latent transforming growth factor beta1 activation in situ: quantitative and functional evidence after low-dose gamma-irradiation. FASEB J 1997;11:991–1002.
crossref pmid
59. Anscher MS, Marks LB, Shafman TD, et al. Risk of long-term complications after TFG-beta1-guided very-high-dose thoracic radiotherapy. Int J Radiat Oncol Biol Phys 2003;56:988–95.
crossref pmid
60. Tsushima H, Kawata S, Tamura S, et al. High levels of transforming growth factor beta 1 in patients with colorectal cancer: association with disease progression. Gastroenterology 1996;110:375–82.
crossref pmid
61. Morris JC, Tan AR, Olencki TE, et al. Phase I study of GC1008 (fresolimumab): a human anti-transforming growth factorbeta (TGFβ) monoclonal antibody in patients with advanced malignant melanoma or renal cell carcinoma. PLoS One 2014;9:e90353.
crossref pmid pmc
62. Bouquet F, Pal A, Pilones KA, er al. TGFβ1 inhibition increases the radiosensitivity of breast cancer cells in vitro and promotes tumor control by radiation in vivo. Clin Cancer Res 2011;17:6754–65.
crossref pmid pmc
63. Formenti SC, Lee P, Adams S, et al. Focal irradiation and systemic TGFβ Blockade in metastatic breast cancer. Clin Cancer Res 2018;24:2493–504.
crossref pmid
64. Liang H, Deng L, Hou Y, et al. Host STING-dependent MDSC mobilization drives extrinsic radiation resistance. Nat Commun 2017;8:1736.
crossref pmid pmc pdf
65. Son CH, Bae JH, Shin DY, et al. Combination effect of regulatory T-cell depletion and ionizing radiation in mouse models of lung and colon cancer. Int J Radiat Oncol Biol Phys 2015;92:390–8.
crossref pmid
66. Kim JH, Jenrow KA, Brown SL. Mechanisms of radiationinduced normal tissue toxicity and implications for future clinical trials. Radiat Oncol J 2014;32:103–15.
crossref pmid pmc
67. Sharlow ER, Leimgruber S, Lira A, et al. A small molecule screen exposes mTOR signaling pathway involvement in radiation-induced apoptosis. ACS Chem Biol 2016;11:1428–37.
crossref pmid pmc
68. Lawrence J, Nho R. The role of the mammalian target of rapamycin (mTOR) in pulmonary fibrosis. Int J Mol Sci 2018;19:E778.
crossref pmid
69. Taniguchi CM, Miao YR, Diep AN, et al. PHD inhibition mitigates and protects against radiation-induced gastrointestinal toxicity via HIF2. Sci Transl Med 2014;6:236ra64.
crossref pmid pmc
70. Olcina MM, Giaccia AJ. Reducing radiation-induced gastrointestinal toxicity: the role of the PHD/HIF axis. J Clin Invest 2016;126:3708–15.
crossref pmid pmc
71. Richardson RB. Ionizing radiation and aging: rejuvenating an old idea. Aging (Albany NY) 2009;1:887–902.
crossref pmid pmc
72. Wang Y, Schulte BA, LaRue AC, Ogawa M, Zhou D. Total body irradiation selectively induces murine hematopoietic stem cell senescence. Blood 2006;107:358–66.
crossref pmid pmc
73. Day RM, Snow AL, Panganiban RA. Radiation-induced accelerated senescence: a fate worse than death? Cell Cycle 2014;13:2011–2.
crossref pmid pmc
74. Wang Y, Boerma M, Zhou D. Ionizing radiation-induced endothelial cell senescence and cardiovascular diseases. Radiat Res 2016;186:153–61.
crossref pmid pmc
75. Pan J, Li D, Xu Y, et al. Inhibition of Bcl-2/xl with ABT-263 selectively kills senescent type II pneumocytes and reverses persistent pulmonary fibrosis induced by ionizing radiation in mice. Int J Radiat Oncol Biol Phys 2017;99:353–61.
crossref pmid
76. Panganiban RA, Day RM. Inhibition of IGF-1R prevents ionizing radiation-induced primary endothelial cell senescence. PLoS One 2013;8:e78589.
crossref pmid pmc
77. Kim JH, Kolozsavry A, Brown SL, et al. Senolytics mitigate radiation-induced normal tissue damage. In: Proceedings of the 64th Annual Radiation Research Society Meeting; 2018 Sep 23-26; Chicago, IL.

78. Kirkland JL, Tchkonia T. Cellular senescence: a translational perspective. EBioMedicine 2017;21:21–8.
crossref pmid pmc
79. Fuhrmann-Stroissnigg H, Ling YY, Zhao J, et al. Identification of HSP90 inhibitors as a novel class of senolytics. Nat Commun 2017;8:422.
crossref pmid pmc pdf
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