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Impact of Cancer Predisposition and Radiosensitivity on the Population Risk of Radiation-Induced Cancers

机译:癌症易感性和放射敏感性对辐射诱发癌症人群风险的影响

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This paper provides a brief overview of the current evidence for cancer predisposition and for an increased sensitivity of individuals carrying such predisposing mutations to cancers induced by ionizing radiations. We also discuss the use of a Mendelian one-locus, two-allele autosomal dominant model for predicting the impact of cancer predisposition and increased radiosensitivity on the risk of radiation-induced cancers in the population and in relatives of affected individuals using breast cancer due to BRCA1 mutations as an example. The main conclusions are the following: (1) The relative risk ratio of the risks of radiation-induced cancer in a heterogeneous population which has subgroups of normal and cancer-predisposed individuals to the risks in a homogeneous population (i.e., one which does not have these subgroups) increases with increasing dose; however, the dose dependence of the RR decreases at higher doses because of the fact that at high doses, the radiation risk to a homogeneous population will already be high. (2) The attributable risk (the proportion of cancers attributable to increased cancer susceptibility and increased radiosensitivity) follows a similar pattern. (3) When the proportion of cancers due to the susceptible genotypes is small (<10%), as is likely to be the case for breast cancers in non-Ashkenazi Jewish women, the increases in risk ratios and attributable risks are small, and become marked only when there are very large increases in cancer susceptibility (>1000-fold) and radiosensitivity (>100-fold) in the susceptible group. (4) When the proportion of cancers due to the susceptible genotypes is appreciable (≥10%), as may be the case for breast cancers in Ashkenazi Jewish women, there may be significant increases in the risk ratios and attributable risk for comparatively moderate increases in cancer susceptibility (>10-fold) and radiosensitivity (>100-fold) in the susceptible subpopulation. (5) The ratio of the risk of radiation-induced cancer in relatives to that in unrelated individuals in the population increases with the biological relatedness of the relative, being higher for close than for distant relatives; however, even when the mutant BRCA1 gene frequency and the proportion of breast cancers due to these mutations are high, as in Ashkenazi Jewish women, for values of predisposition strength and radiosensitivity differential <10, the increase in breast cancer risks is only marginal, even for first-degree relatives.
机译:本文简要概述了癌症易感性的当前证据以及携带此类易感性突变的个体对电离辐射诱发的癌症的敏感性提高。我们还讨论了使用孟德尔单基因座,两等位基因常染色体显性模型预测癌症易感性和放射敏感性增加对人群和受乳腺癌影响的亲属的辐射诱发癌症风险的影响。以BRCA1突变为例。主要结论如下:(1)在具有正常人群和癌症易感人群的亚类人群中,辐射致癌风险的相对危险度与在同质人群中的相对危险度之比(即没有这些亚组)随着剂量的增加而增加;然而,由于高剂量时,RR的剂量依赖性降低,因为在高剂量时,对同质群体的辐射风险已经很高。 (2)归因风险(归因于癌症易感性和放射敏感性增加的癌症比例)遵循相似的模式。 (3)当由于易感基因型导致的癌症比例很小(<10%)时(非非阿什肯纳兹犹太妇女很可能患乳腺癌),风险比率和可归因风险的增加很小,并且仅在易感人群中癌症易感性(> 1000倍)和放射敏感性(> 100倍)大大增加时才显着。 (4)当由于易感基因型导致的癌症比例相当大(≥10%)时(例如阿什肯纳齐犹太妇女的乳腺癌),风险比率可能会显着增加,而适度增加的可归因的风险可能会增加易感亚群的癌症易感性(> 10倍)和放射敏感性(> 100倍)。 (5)人口中由亲属引起的辐射致癌风险与人群中无亲属的风险的比率随亲属的生物学亲缘关系而增加,近亲比远亲更高。然而,即使突变BRCA1基因的频率和由于这些突变而导致的乳腺癌比例很高,例如在Ashkenazi犹太妇女中,对于易感强度和放射敏感性差异值<10,乳腺癌风险的增加也只是微不足道,甚至对于一级亲戚。

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