Harnessing tumor immunogenomics: Tumor neoantigens in ovarian cancer and beyond

被引:7
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
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2023年 / 1878卷 / 06期
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
相关论文
共 140 条
[91]   Adoptive cell transfer as personalized immunotherapy for human cancer [J].
Rosenberg, Steven A. ;
Restifo, Nicholas P. .
SCIENCE, 2015, 348 (6230) :62-68
[92]   Education Forum I: Immunotherapy 2018: Updates and Toxicities Saturday, March 24, 2018 [J].
Ross, M. S. ;
Tianzhou, M. ;
Priedigkeit, N. ;
Zhang, L. ;
Tseng, G. ;
Lee, A. V. ;
Edwards, R. P. ;
Vlad, A. .
GYNECOLOGIC ONCOLOGY, 2018, 149 :8-8
[93]   Resistance to checkpoint blockade therapy through inactivation of antigen presentation [J].
Sade-Feldman, Moshe ;
Jiao, Yunxin J. ;
Chen, Jonathan H. ;
Rooney, Michael S. ;
Barzily-Rokni, Michal ;
Eliane, Jean-Pierre ;
Bjorgaard, Stacey L. ;
Hammond, Marc R. ;
Vitzthum, Hans ;
Blackmon, Shauna M. ;
Frederick, Dennie T. ;
Hazar-Rethinam, Mehlika ;
Nadres, Brandon A. ;
Van Seventer, Emily E. ;
Shukla, Sachet A. ;
Yizhak, Keren ;
Ray, John P. ;
Rosebrock, Daniel ;
Livitz, Dimitri ;
Adalsteinsson, Viktor ;
Getz, Gad ;
Duncan, Lyn M. ;
Li, Bo ;
Corcoran, Ryan B. ;
Lawrence, Donald P. ;
Stemmer-Rachamimov, Anat ;
Boland, Genevieve M. ;
Landau, Dan A. ;
Flaherty, Keith T. ;
Sullivan, Ryan J. ;
Hacohen, Nir .
NATURE COMMUNICATIONS, 2017, 8
[94]   Potential clinical application of tumor-infiltrating lymphocyte therapy for ovarian epithelial cancer prior or post-resistance to chemotherapy [J].
Sakellariou-Thompson, Donastas ;
Forget, Marie-Andree ;
Hinchcliff, Emily ;
Celestino, Joseph ;
Hwu, Patrick ;
Jazaeri, Amir A. ;
Haymaker, Cara ;
Bernatchez, Chantale .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2019, 68 (11) :1747-1757
[95]   Phenotypic and functional analysis of tumor-infiltrating lymphocytes compared with tumor-associated lymphocytes from ascitic fluid and peripheral blood lymphocytes in patients with advanced ovarian cancer [J].
Santin, AD ;
Hermonat, PL ;
Ravaggi, A ;
Bellone, S ;
Roman, JJ ;
Smith, CV ;
Pecorelli, S ;
Radominska-Pandya, A ;
Cannon, MJ ;
Parham, GP .
GYNECOLOGIC AND OBSTETRIC INVESTIGATION, 2001, 51 (04) :254-261
[96]   A Phase I/II trial comparing autologous dendritic cell vaccine pulsed either with personalized peptides (PEP-DC) or with tumor lysate (OC-DC) in patients with advanced high-grade ovarian serous carcinoma [J].
Sarivalasis, Apostolos ;
Boudousquie, Caroline ;
Balint, Klara ;
Stevenson, Brian J. ;
Gannon, Philippe O. ;
Iancu, Emanuela Marina ;
Rossier, Laetitia ;
Lluesma, Silvia Martin ;
Mathevet, Patrice ;
Sempoux, Christine ;
Coukos, George ;
Dafni, Urania ;
Harari, Alexandre ;
BassaniSternberg, Michal ;
Kandalaft, Lana E. .
JOURNAL OF TRANSLATIONAL MEDICINE, 2019, 17 (01)
[97]   Intraepithelial CD8+ tumor-infiltrating lymphocytes and a high CD8+/regulatory T cell ratio are associated with favorable prognosis in ovarian cancer [J].
Sato, E ;
Olson, SH ;
Ahn, J ;
Bundy, B ;
Nishikawa, H ;
Qian, F ;
Jungbluth, AA ;
Frosina, D ;
Gnjatic, S ;
Ambrosone, C ;
Kepner, J ;
Odunsi, T ;
Ritter, G ;
Lele, S ;
Chen, YT ;
Ohtani, H ;
Old, LJ ;
Odunsi, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (51) :18538-18543
[98]   Immunotherapy and Its Development for Gynecological (Ovarian, Endometrial and Cervical) Tumors: From Immune Checkpoint Inhibitors to Chimeric Antigen Receptor (CAR)-T Cell Therapy [J].
Schepisi, Giuseppe ;
Casadei, Chiara ;
Toma, Ilaria ;
Poti, Giulia ;
Iaia, Maria Laura ;
Farolfi, Alberto ;
Conteduca, Vincenza ;
Lolli, Cristian ;
Ravaglia, Giorgia ;
Brighi, Nicole ;
Altavilla, Amelia ;
Martinelli, Giovanni ;
De Giorgi, Ugo .
CANCERS, 2021, 13 (04) :1-22
[99]   Neoantigens in cancer immunotherapy [J].
Schumacher, Ton N. ;
Schreiber, Robert D. .
SCIENCE, 2015, 348 (6230) :69-74
[100]   CD4+ T-cell recognition of mutated B-RAF in melanoma patients harboring the V599E mutation [J].
Sharkey, MS ;
Lizée, G ;
Gonzales, MI ;
Patel, S ;
Topalian, SL .
CANCER RESEARCH, 2004, 64 (05) :1595-1599