首页> 外文期刊>The Journal of Pathology: Clinical Research >Association of p16 expression with prognosis varies across ovarian carcinoma histotypes: an Ovarian Tumor Tissue Analysis consortium study
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Association of p16 expression with prognosis varies across ovarian carcinoma histotypes: an Ovarian Tumor Tissue Analysis consortium study

机译:p16表达与预后的关联因卵巢癌组织类型而异:卵巢肿瘤组织分析联合会研究

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We aimed to validate the prognostic association of p16 expression in ovarian high‐grade serous carcinomas (HGSC) and to explore it in other ovarian carcinoma histotypes. p16 protein expression was assessed by clinical‐grade immunohistochemistry in 6525 ovarian carcinomas including 4334 HGSC using tissue microarrays from 24 studies participating in the Ovarian Tumor Tissue Analysis consortium. p16 expression patterns were interpreted as abnormal (either overexpression referred to as block expression or absence) or normal (heterogeneous). CDKN2A (which encodes p16) mRNA expression was also analyzed in a subset ( n = 2280) mostly representing HGSC ( n = 2010). Association of p16 expression with overall survival (OS) was determined within histotypes as was CDKN2A expression for HGSC only. p16 block expression was most frequent in HGSC (56%) but neither protein nor mRNA expression was associated with OS. However, relative to heterogeneous expression, block expression was associated with shorter OS in endometriosis‐associated carcinomas, clear cell [hazard ratio (HR): 2.02, 95% confidence (CI) 1.47–2.77, p 0.001] and endometrioid (HR: 1.88, 95% CI 1.30–2.75, p = 0.004), while absence was associated with shorter OS in low‐grade serous carcinomas (HR: 2.95, 95% CI 1.61–5.38, p = 0.001). Absence was most frequent in mucinous carcinoma (50%), and was not associated with OS in this histotype. The prognostic value of p16 expression is histotype‐specific and pattern dependent. We provide definitive evidence against an association of p16 expression with survival in ovarian HGSC as previously suggested. Block expression of p16 in clear cell and endometrioid carcinoma should be further validated as a prognostic marker, and absence in low‐grade serous carcinoma justifies CDK4 inhibition.
机译:我们旨在验证p16表达在卵巢高级浆液性癌(HGSC)中的预后相关性,并探讨其在其他卵巢癌组织学类型中的作用。使用来自卵巢肿瘤组织分析联盟的24项研究的组织芯片,​​通过临床级免疫组织化学对6525例卵巢癌(包括4334 HGSC)中的p16蛋白表达进行了评估。 p16表达模式被解释为异常(过表达称为嵌段表达或缺失)或正常(异源)。还分析了CDKN2A(编码p16)mRNA表达的子集(n = 2280),主要代表HGSC(n = 2010)。 p16表达与总生存期(OS)的关联在组织型中得以确定,CDKN2A表达仅用于HGSC。在HGSC中,p16的表达最为频繁(56%),但蛋白和mRNA的表达均与OS无关。然而,相对于异质表达,在子宫内膜异位症相关癌中,阻滞表达与较短的OS,透明细胞[危险比(HR):2.02、95%置信度(CI)1.47–2.77,p <0.001]和子宫内膜样物质(HR: 1.88,95%CI 1.30-2.75,p = 0.004),而缺席与低度浆液性癌的OS短相关(HR:2.95,95%CI 1.61-5.38,p = 0.001)。黏液癌的缺席率最高(50%),在这种组织型中与OS无关。 p16表达的预后价值取决于组织类型和模式。我们提供了明确的证据,以证明p16表达与卵巢HGSC的存活相关。 p16在透明细胞和子宫内膜样癌中的阻滞表达应进一步作为预后标志物,而低度浆液性癌的缺失可证明对CDK4的抑制作用。

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