Перейти к основному содержанию
AkademIndex

Продукты

Для разработчиков

AkademBaseОткрытый API экосистемы
Обзорная статья

T‐cell immunoglobulin and ITIM domain, as a potential immune checkpoint target for immunotherapy of colorectal cancer

Mehrdad FathiCancer and Immunology Research Center Kurdistan University of Medical Sciences Sanandaj IranInna PustokhinaKazan Federal University Kazan RussiaSergey V. KuznetsovI.M. Sechenov First Moscow State Medical University (Sechenov University) Moscow RussiaMars KhayrullinDepartment of Research Management, K.G. Razumovsky Moscow State University of Technologies and Management (The First Cossack University) Moscow Russian FederationMohammad Hojjat‐FarsangiBioclinicum, Department of Oncology‐Pathology Karolinska Institute Stockholm SwedenVahid KarpishehDepartment of Immunology, School of Medicine Tabriz University of Medical Sciences Tabriz IranAli JaliliCancer and Immunology Research Center Kurdistan University of Medical Sciences Sanandaj IranFarhad Jadidi‐NiaraghDepartment of Immunology, School of Medicine Tabriz University of Medical Sciences Tabriz Iran
2021en
ABI

Аннотация

The importance of the tumor microenvironment in cancer progression has been well studied for many years. Immune checkpoint inhibitors (ICIs) are regarded as potential strategies in enhancing the immune responses in patients with cancer, particularly colorectal cancer (CRC). Notably, CRCs are extraordinarily heterogeneous and mostly are microsatellite-stable (MSS) or cold tumors, which means that the immune response is not usually as strong as that of foreign cells. T-cell immunoglobulin and ITIM domain (TIGIT) is a new immune checkpoint receptor overexpressed inside the CRC tumor-immune microenvironments. Moreover, several studies have shown that TIGIT in combination with other ICIs and/or conventional treatments, can lead to a robust anti-tumor response in CRC. This review looks deep inside TIGIT expression patterns, their various functions, and possible immunotherapy strategies to increase survival rates and decrease immune-related adverse events.

Перевод пока недоступен

Идентификаторы

Цитирования и источники

Цитирований: 3Использованных источников: 0