MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1073/pnas.1402714111

Медицинская библиотека · Proceedings of the National Academy of Sciences of the United States of America · 2014

Microvesicles containing miRNAs promote muscle cell death in cancer cachexia via TLR7.

He Wei A, Calore Federica, Londhe Priya, Canella Alessandro, Guttridge Denis C, Croce Carlo M

СтатьяПоддержка NIH: внешняя программаПеревод в очереди

Аннотация

MicroRNAs (miRNAs) are small, noncoding RNAs that regulate gene expression and, in cancers, are often packaged within secreted microvesicles. The cachexia syndrome is a debilitating state of cancer that predominantly results from the loss of skeletal muscle mass, which is in part associated with apoptosis. How tumors promote apoptosis in distally located skeletal muscles has not been explored. Using both tumor cell lines and patient samples, we show that tumor-derived microvesicles induce apoptosis of skeletal muscle cells. This proapoptotic activity is mediated by a microRNA cargo, miR-21, which signals through the Toll-like 7 receptor (TLR7) on murine myoblasts to promote cell death. Furthermore, tumor microvesicles and miR-21 require c-Jun N-terminal kinase activity to regulate this apoptotic response. Together, these results describe a unique pathway by which tumor cells promote muscle loss, which might provide a great insight into elucidating the causes and treatment options of cancer cachexia.

Для цитирования: He Wei A, Calore Federica, Londhe Priya, Canella Alessandro, Guttridge Denis C, Croce Carlo M. Microvesicles containing miRNAs promote muscle cell death in cancer cachexia via TLR7.. Proceedings of the National Academy of Sciences of the United States of America. 2014. DOI: 10.1073/pnas.1402714111.

Предметные рубрики MeSH

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.