Harnessing tumor immunogenomics: Tumor neoantigens in ovarian cancer and beyond

被引:5
|
作者
Wu, Mengrui [1 ]
Zhou, Shengtao [1 ]
机构
[1] Sichuan Univ, West China Hosp 2, Dept Obstet & Gynecol, Key Lab Birth Defects & Related Dis Women & Childr, Chengdu, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Ovarian cancer; Immunogenomics; Next -generation sequencing; Neoantigen; Immunotherapy; CYTOLYTIC T-LYMPHOCYTES; INFILTRATING LYMPHOCYTES; CELL RESPONSES; PROGNOSTIC-SIGNIFICANCE; ADOPTIVE TRANSFER; CTLA-4; BLOCKADE; HUMAN-MELANOMA; PD-1; GENE FUSIONS; IMMUNOTHERAPY;
D O I
10.1016/j.bbcan.2023.189017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ovarian cancer is a major cause of death among gynecological cancers due to its highly aggressive nature. Immunotherapy has emerged as a promising avenue for ovarian cancer treatment, offering targeted approaches with reduced off-target effects. With the advent of next-generation sequencing, it has become possible to identify genomic alterations that can serve as potential targets for immunotherapy. Furthermore, immunogenomics research has revealed the importance of genetic alterations in shaping the cancer immune responses. However, the heterogeneity of immunogenicity and the low tumor mutation burden pose challenges for neoantigen-based immunotherapies. Further research is needed to identify neoantigen-specific tumor-infiltrating lymphocytes (TIL) and establish guidelines for patient inclusion criteria in TIL-based therapy. The study of neoantigens and their implications in ovarian cancer immunotherapy holds great promise, and efforts focused on personalized treatment strategies, refined neoantigen selection, and optimized therapeutic combinations will contribute to improving patient outcomes in the future.
引用
收藏
页数:16
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