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


ABSTRACT: 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.

SUBMITTER: He WA 

PROVIDER: S-EPMC3970508 | biostudies-literature | 2014 Mar

REPOSITORIES: biostudies-literature

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

He Wei A WA   Calore Federica F   Londhe Priya P   Canella Alessandro A   Guttridge Denis C DC   Croce Carlo M CM  

Proceedings of the National Academy of Sciences of the United States of America 20140310 12


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 apopto  ...[more]

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2022-02-04 | GSE144512 | GEO