APOBEC3B stratifies ovarian clear cell carcinoma with distinct immunophenotype and prognosis

被引:3
作者
Long, Xiaoran [1 ,2 ]
Lu, Huaiwu [3 ]
Cai, Mei-Chun [1 ]
Zang, Jingyu [1 ]
Zhang, Zhuqing [1 ,2 ]
Wu, Jie [4 ]
Liu, Xiaoshi [1 ,2 ]
Cheng, Lin [1 ,2 ]
Cheng, Jiejun [5 ]
Cheung, Lydia W. T. [6 ]
Shen, Zhen [7 ]
Zhou, Ying [7 ]
Di, Wen [1 ,2 ]
Zhuang, Guanglei [1 ,2 ]
Yin, Xia [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Ren Ji Hosp, Shanghai Key Lab Gynecol Oncol, Sch Med, Shanghai, Peoples R China
[3] Sun Yat Sen Univ, Sun Yat sen Mem Hosp, Dept Gynecol Oncol, Guangzhou, Peoples R China
[4] Qingdao Univ, Dept Pathol, Affiliated Hosp, Qingdao, Peoples R China
[5] Shanghai Jiao Tong Univ, Ren Ji Hosp, Dept Radiol, Sch Med, Shanghai, Peoples R China
[6] Univ Hong Kong, Li Ka Shing Fac Med, Sch Biomed Sci, Hong Kong, Peoples R China
[7] Univ Sci & Technol China, Affiliated Hosp USTC 1, Dept Obstet & Gynecol, Div Life Sci & Med, Hefei, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
MUTATIONAL SIGNATURES; DEAMINASE APOBEC3B; ANTITUMOR-ACTIVITY; CANCER GENOMES; EVOLUTION; HETEROGENEITY; MUTAGENESIS; EXPRESSION; SAFETY; LINES;
D O I
10.1038/s41416-023-02239-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundOvarian clear cell carcinoma (OCCC) is a challenging disease due to its intrinsic chemoresistance. Immunotherapy is an emerging treatment option but currently impeded by insufficient understanding of OCCC immunophenotypes and their molecular determinants.MethodsWhole-genome sequencing on 23 pathologically confirmed patients was employed to depict the genomic profile of primary OCCCs. APOBEC3B expression and digital pathology-based Immunoscore were assessed by performing immunohistochemistry and correlated with clinical outcomes.ResultsAn APOBEC-positive (APOBEC+) subtype was identified based on the characteristic mutational signature and prevalent kataegis events. APOBEC + OCCC displayed favourable prognosis across one internal and two external patient cohorts. The improved outcome was ascribable to increased lymphocytic infiltration. Similar phenomena of APOBEC3B expression and T-cell accumulation were observed in endometriotic tissues, suggesting that APOBEC-induced mutagenesis and immunogenicity could occur early during OCCC pathogenesis. Corroborating these results, a case report was presented for an APOBEC + patient demonstrating inflamed tumour microenvironment and clinical response to immune checkpoint blockade.ConclusionsOur findings implicate APOBEC3B as a novel mechanism of OCCC stratification with prognostic value and as a potential predictive biomarker that may inform immunotherapeutic opportunities.
引用
收藏
页码:2054 / 2062
页数:9
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