CDK12在实体肿瘤中的失活:一种可操作的遗传亚型

C. H. Marshall, E. Imada, Zhuojun Tang, L. Marchionni, E. Antonarakis
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引用次数: 18

摘要

据报道,在卵巢癌和前列腺癌中,CDK12的失活改变可能具有治疗意义;然而,这些突变在其他癌症类型中的流行程度尚不清楚。我们检索了cbiopportal和GENIE Project(公开发布版本v4.1)数据库,寻找有bbbb200例测序病例的癌症类型,包括转移性疾病患者,其中至少发生单等位基因CDK12改变的发生率为b>1%。至少单等位基因CDK12突变的患病率在膀胱癌中最高(3.7%);其次是前列腺癌(3.4%)、食管胃癌(2.1%)和子宫癌(2.1%)。双等位基因CDK12失活在前列腺癌中最高(1.8%),其次是卵巢癌(1.0%)和膀胱癌(0.5%)。这些结果是第一次(据我们所知)估计单等位基因和双等位基因CDK12突变在超过15,000例的多种癌症类型中的患病率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CDK12 inactivation across solid tumors: an actionable genetic subtype
Inactivating CDK12 alterations have been reported in ovarian and prostate cancers and may have therapeutic implications; however, the prevalence of these mutations across other cancer types is unknown. We searched the cBioPortal and GENIE Project (public release v4.1) databases for cancer types with > 200 sequenced cases, that included patients with metastatic disease, and in which the occurrence of at least monoallelic CDK12 alterations was > 1%. The prevalence of at least monoallelic CDK12 mutations was highest in bladder cancer (3.7%); followed by prostate (3.4%), esophago-gastric (2.1%) and uterine cancers (2.1%). Biallelic CDK12 inactivation was highest in prostate cancer (1.8%), followed by ovarian (1.0%) and bladder cancers (0.5%). These results are the first (to our knowledge) to estimate the prevalence of monoallelic and biallelic CDK12 mutations across multiple cancer types encompassing over 15,000 cases.
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