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Biological Complexities in Radiation Carcinogenesis and Cancer Radiotherapy: Impact of New Biological Paradigms

机译:放射致癌和癌症放射治疗中的生物复杂性:新的生物学范例的影响

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摘要

Although radiation carcinogenesis has been shown both experimentally and epidemiologically, the use of ionizing radiation is also one of the major modalities in cancer treatment. Various known cellular and molecular events are involved in carcinogenesis. Apart from the known phenomena, there could be implications for carcinogenesis and cancer prevention due to other biological processes such as the bystander effect, the abscopal effect, intrinsic radiosensitivity and radioadaptation. Bystander effects have consequences for mutation initiated cancer paradigms of radiation carcinogenesis, which provide the mechanistic justification for low-dose risk estimates. The abscopal effect is potentially important for tumor control and is mediated through cytokines and/or the immune system (mainly cell-mediated immunity). It results from loss of growth and stimulatory and/or immunosuppressive factors from the tumor. Intrinsic radiosensitivity is a feature of some cancer prone chromosomal breakage syndromes such as ataxia telangectiasia. Radiosensitivity is manifested as higher chromosomal aberrations and DNA repair impairment is now known as a good biomarker for breast cancer screening and prediction of prognosis. However, it is not yet known whether this effect is good or bad for those receiving radiation or radiomimetic agents for treatment. Radiation hormesis is another major concern for carcinogenesis. This process which protects cells from higher doses of radiation or radio mimic chemicals, may lead to the escape of cells from mitotic death or apoptosis and put cells with a lower amount of damage into the process of cancer induction. Therefore, any of these biological phenomena could have impact on another process giving rise to genome instability of cells which are not in the field of radiation but still receiving a lower amount of radiation. For prevention of radiation induced carcinogenesis or risk assessment as well as for successful radiation therapy, all these phenomena should be taken into account.
机译:尽管已经通过实验和流行病学方法证明了放射致癌作用,但电离辐射的使用也是癌症治疗的主要方式之一。各种已知的细胞和分子事件都参与致癌作用。除了已知的现象外,由于其他生物学过程,例如旁观者效应,抽象效应,内在放射敏感性和放射适应性,还可能对致癌和癌症预防产生影响。旁观者效应对辐射致癌的突变引发的癌症范例有影响,这些范例为低剂量风险评估提供了机械依据。绝对效应对于肿瘤控制可能是重要的,并且是通过细胞因子和/或免疫系统介导的(主要是细胞介导的免疫)。它是由于肿瘤的生长以及刺激和/或免疫抑制因子的丧失所致。固有放射敏感性是某些癌症易发染色体断裂综合征(例如共济失调性毛细血管扩张症)的特征。放射敏感性表现为较高的染色体畸变,而DNA修复受损现被认为是乳腺癌筛查和预测预后的良好生物标志物。然而,对于接受放射或放射模拟剂治疗的人,这种效果是好是坏还不知道。辐射致癌是致癌的另一个主要问题。该过程保护细胞免受更高剂量的辐射或放射模拟化学物质的侵害,可能导致细胞逃脱有丝分裂死亡或凋亡,并使受损程度较低的细胞进入癌症诱导过程。因此,这些生物现象中的任何一种都可能影响另一个过程,从而导致不在辐射领域但仍接受较少辐射量的细胞的基因组不稳定。为了防止放射线致癌或风险评估以及成功的放射线治疗,应考虑所有这些现象。

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