Association of recurrent APOBEC3B alterations with the prognosis of gastric-type cervical adenocarcinoma

医学 腺癌 CDKN2A 癌症 外显子组测序 人口 病理 内科学 肿瘤科 生物 突变 遗传学 基因 环境卫生
作者
Xin Liao,Xuyang Xia,Su Wei,Huayun Yan,Yingfang Ma,Lian Xu,Han Luo,Wanting Liu,Dandan Yin,Weihan Zhang,Hai‐Ning Chen,Yu Deng,Zhixiang Ren,Zehui Yu,Fei Liao,Keling Chen,Minyuan Cao,Yiguan Zhang,Zhang Wei,Wei Wang,Junning Zhao,Huan Xu,Yang Shu
出处
期刊:Gynecologic Oncology [Elsevier]
卷期号:165 (1): 105-113 被引量:8
标识
DOI:10.1016/j.ygyno.2022.01.036
摘要

Gastric-type cervical adenocarcinoma (GCA) is a rare and aggressive type of endocervical adenocarcinoma (ECA) with distinct histopathologic features and unfavorable treatment outcomes, but no genomic prognostic factor has been revealed. We aimed to systematically investigate the somatic alterations of GCA at genome-wide level and evaluate their prognostic value.We performed whole-exome sequencing (WES) on 25 pairs of tumor and matched normal samples to characterize the genomic features of Chinese patients with GCA and investigated their relations to histopathological characterizations and prognosis. The prognostic value of the genomic alterations was evaluated in a total of 58 GCA patients.Mutations were commonly observed in reported GCA-related driver genes, including TP53 (32%), CDKN2A (20%), SKT11 (20%), BRCA2 (12%), SMAD4 (12%), and ERBB2 (12%). Recurrent novel trunk mutations were also observed in PBRM1 (12%), FRMPD4 (12%), and NOP2 (8%) with high variant allele frequency. Moreover, enrichment of the APOBEC signature was attributed to frequent gain of somatic copy number alteration (SCNA) of APOBEC3B (20%), which perfectly matched the nuclear-positive staining of APOBEC3B through immunohistochemistry. In contrast, APOBEC3B alteration was absent in patients with conventional type of ECA (N = 52). Notably, positive APOBEC3B was consistently enriched in patients with favorable prognosis in both the discovery cohort and an additional 33 GCA patients, thus indicating a significant association with lower relapse risk of GCA independent of cancer stage (P = 0.02).Our results can aid understanding of the molecular basis of GCA in the Chinese population by providing genomic profiles and highlighting the potential prognostic value of APOBEC3B for GCA through routine clinical IHC.
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