TY - JOUR
T1 - Immunomodulatory effects of radiotherapy
AU - Kumari, Sharda
AU - Mukherjee, Shibani
AU - Sinha, Debapriya
AU - Abdisalaam, Salim
AU - Krishnan, Sunil
AU - Asaithamby, Aroumougame
N1 - Funding Information:
Funding: This work was supported by the National Institutes of Health grant R01AG053341 (to A.A.) and the Cancer Prevention and Research Institute of Texas grant RP190435 (to A.A.).
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/11/1
Y1 - 2020/11/1
N2 - Radiation therapy (RT), an integral component of curative treatment for many malignancies, can be administered via an increasing array of techniques. In this review, we summarize the properties and application of different types of RT, specifically, conventional therapy with x-rays, stereotactic body RT, and proton and carbon particle therapies. We highlight how low-linear energy transfer (LET) radiation induces simple DNA lesions that are efficiently repaired by cells, whereas high-LET radiation causes complex DNA lesions that are difficult to repair and that ultimately enhance cancer cell killing. Additionally, we discuss the immunogenicity of radiation-induced tumor death, elucidate the molecular mechanisms by which radiation mounts innate and adaptive immune responses and explore strategies by which we can increase the efficacy of these mechanisms. Understanding the mechanisms by which RT modulates immune signaling and the key players involved in modulating the RT-mediated immune response will help to improve therapeutic efficacy and to identify novel immunomodulatory drugs that will benefit cancer patients undergoing targeted RT.
AB - Radiation therapy (RT), an integral component of curative treatment for many malignancies, can be administered via an increasing array of techniques. In this review, we summarize the properties and application of different types of RT, specifically, conventional therapy with x-rays, stereotactic body RT, and proton and carbon particle therapies. We highlight how low-linear energy transfer (LET) radiation induces simple DNA lesions that are efficiently repaired by cells, whereas high-LET radiation causes complex DNA lesions that are difficult to repair and that ultimately enhance cancer cell killing. Additionally, we discuss the immunogenicity of radiation-induced tumor death, elucidate the molecular mechanisms by which radiation mounts innate and adaptive immune responses and explore strategies by which we can increase the efficacy of these mechanisms. Understanding the mechanisms by which RT modulates immune signaling and the key players involved in modulating the RT-mediated immune response will help to improve therapeutic efficacy and to identify novel immunomodulatory drugs that will benefit cancer patients undergoing targeted RT.
KW - Abscopal effects
KW - Cancer vaccines
KW - Carbon ion therapy
KW - Charged particle therapy
KW - Clustered DNA damage
KW - FLASH-RT
KW - Immune signaling
KW - Radiation therapy
KW - Tumor antigens
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U2 - 10.3390/ijms21218151
DO - 10.3390/ijms21218151
M3 - Review article
C2 - 33142765
AN - SCOPUS:85095581310
SN - 1661-6596
VL - 21
SP - 1
EP - 29
JO - International journal of molecular sciences
JF - International journal of molecular sciences
IS - 21
M1 - 8151
ER -