MedElevator Войти в исследования
← Поиск публикаций

DOI 10.3892/ol.2026.15866

Медицинская библиотека · Oncology letters · 2026

Role of tumor necrosis factor receptor superfamily member 19 in cancer: Diverse functions and therapeutic potential (Review).

Xu Manyu, Liu Zhaoyang, Zhang Jingyu, Xu Hanyun, Xu Yufei, Zhang Yue, Hu Qiong-Ying, Zhang Tao

СтатьяОбзорПеревод в очереди

Аннотация

Tumor necrosis factor receptor superfamily member 19 (TNFRSF19), as a principal member of the TNFRSF, is highly expressed across a variety of invasive neoplastic diseases. It facilitates the evasion of host anti-cancer immune responses by remodelling the immunosuppressive cancer microenvironment, thereby playing a key role in immune evasion; conversely, inhibiting its expression can significantly delay cancer progression. This article provides a systematic review of the functional diversity of this molecule, its encoding of two functionally distinct isoforms via differential transcription initiation, the mechanisms underlying its pro-cancer and anti-cancer effects in various cancer diseases, and its potential value in targeted intervention strategies, clinical translation and the regulation of the cancer immune microenvironment, thereby providing a theoretical foundation for further mechanistic investigations in oncology and for the development of combinatorial immunotherapeutic regimens incorporating TNFRSF19-targeted interventions.

Для цитирования: Xu Manyu, Liu Zhaoyang, Zhang Jingyu, Xu Hanyun, Xu Yufei, Zhang Yue, Hu Qiong-Ying, Zhang Tao. Role of tumor necrosis factor receptor superfamily member 19 in cancer: Diverse functions and therapeutic potential (Review).. Oncology letters. 2026. DOI: 10.3892/ol.2026.15866.
Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.