Cancer vaccines: Targeting KRAS-driven cancers

被引:40
|
作者
Zhang, Ying [1 ]
Ma, Jin-An [1 ]
Zhang, Hai-Xia [1 ]
Jiang, Yu-Na [1 ]
Luo, Wen-Hao [2 ]
机构
[1] Cent South Univ, Xiangya Hosp 2, Dept Oncol, Changsha 410011, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Dept Gen Surg, Beijing, Peoples R China
关键词
KRAS mutation; neo-antigen vaccine; pancreatic cancer; colorectal cancer; lung cancer; peptide vaccine; LYMPHOBLASTOID CELL-LINES; RAS PEPTIDE VACCINATION; PANCREATIC-CANCER; PHASE-II; MOLECULAR ADJUVANTS; LUNG-CANCER; MUTANT KRAS; OPEN-LABEL; GM-CSF; ONCOGENE;
D O I
10.1080/14760584.2020.1733420
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Mutant KRAS is a genetic driver of multiple cancers that has challenged clinical anti-cancer therapeutics in the last 3 decades. Neo-antigens encoded by KRAS mutations have been identified as tumor-specific with high immunogenicity and can be used to deliver precision cancer vaccines to promote anti-tumor immune responses. KRAS mutation-based cancer vaccines have produced encouraging preclinical and clinical results. Cancer vaccines represent a promising approach to treat KRAS-driven cancers. Areas covered: In this review, we summarize the development and progress of vaccines targeting KRAS and evaluate their potential benefits and obstacles in the current landscape of therapy for KRAS-driven cancers. Expert opinion: KRAS mutation-based cancer vaccines can induce immunogenicity in patients with KRAS-driven cancers. However, the mechanisms of tumor suppression including cellular and molecular factors within the tumor microenvironment may limit vaccine efficacy. Combining KRAS-driven therapeutic cancer vaccines with other methods and adjuvants can circumvent immunosuppression and promote therapeutic successes.
引用
收藏
页码:163 / 173
页数:11
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