在CHEK2中,具有双基生殖系病原体变异的个体的异质癌症表型
Snežana Hinić1, Cezary Cybulski2, Rachel S Van der Post3
1Radboud University Medical Center, Research Institute for Medical Innovation, Department of Human Genetics, Nijmegen, The Netherlands.
概括
双性CHEK2生殖系致病变体 (gPVs) 患者对多种癌症 (包括结直肠癌,甲状腺癌和前列腺癌) 的敏感性增加. 诊断测试的局限性可能导致这些CHEK2变异的诊断不足.
科学领域:
- 遗传学 是一个遗传学.
- 在瘤学瘤学.
- 分子生物学分子生物学
背景情况:
- 在CHEK2中的生殖系致病变体 (gPV) 与遗传性癌症,特别是乳腺癌有关.
- 双基CHEK2 gPV很少见,但与单基变异相比,可能会增加多种原发性恶性瘤的风险.
研究的目的:
- 为了研究与乳腺癌以外的双性CHEK2 gPV相关的恶性瘤的范围.
- 扩大对双性CHEK2功能丧失变体患者癌症易感性的理解.
主要方法:
- 外体序列测序用于识别双性CHEK2 gPVs.个体.
- 收集和分析了来自291名双性CHEK2 gPV患者队列的表型数据.
主要成果:
- 超过一半 (53.4%) 的双性CHEK2 gPV患者至少出现了一种恶性瘤.
- 结肠直肠,甲状腺和前列腺癌是乳腺癌之后最常见的恶性瘤.
- 与具有特定误解变异的女性相比,具有双性CHEK2功能丧失的gPV的女性在较早的年龄内患有多种恶性瘤的发病率更高.
结论:
- 双性CHEK2 gPV增加了女性和男性对多种癌症的易感性.
- 目前对CHEK2变异的诊断测试,通常仅限于乳腺癌患者,可能导致其他恶性瘤患者的诊断不足.
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