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

被引:202
作者
He, Wei A.
Calore, Federica
Londhe, Priya
Canella, Alessandro
Guttridge, Denis C. [1 ]
Croce, Carlo M.
机构
[1] Ohio State Univ, Dept Mol Virol Immunol & Med Genet, Human Canc Genet Program, Columbus, OH 43210 USA
基金
美国国家卫生研究院;
关键词
TLRs; MVs; JNK; muscle stem cells; SKELETAL-MUSCLE; SIGNALING PATHWAYS; MICRORNAS; APOPTOSIS; DYSREGULATION; MECHANISM;
D O I
10.1073/pnas.1402714111
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:4525 / 4529
页数:5
相关论文
共 31 条
[1]   Skeletal muscle apoptosis and weight loss in chronic obstructive pulmonary disease [J].
Agustí, AGN ;
Sauleda, J ;
Miralles, C ;
Gomez, C ;
Togores, B ;
Sala, E ;
Batle, S ;
Busquets, X .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (04) :485-+
[2]  
Alexandrov Peter N, 2012, Int J Biochem Mol Biol, V3, P365
[3]   Circulating microRNAs: New biomarkers in diagnosis, prognosis and treatment of cancer (Review) [J].
Allegra, Alessandro ;
Alonci, Andrea ;
Campo, Salvatore ;
Penna, Giuseppa ;
Petrungaro, Annamaria ;
Gerace, Demetrio ;
Musolino, Caterina .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2012, 41 (06) :1897-1912
[4]   Apoptosis signalling is essential and precedes protein degradation in wasting skeletal muscle during catabolic conditions [J].
Argiles, Josep A. ;
Lopez-Soriano, Francisco J. ;
Busquets, Silvia .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2008, 40 (09) :1674-1678
[5]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[6]   In vivo time-lapse microscopy reveals no loss of murine myonuclei during weeks of muscle atrophy [J].
Bruusgaard, Jo C. ;
Gundersen, Kristian .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (04) :1450-1457
[7]   Apoptosis is present in skeletal muscle of cachectic gastro-intestinal cancer patients [J].
Busquets, Silvia ;
Deans, Chris ;
Figueras, Maite ;
Moore-Carrasco, Rodrigo ;
Lopez-Soriano, Francisco J. ;
Fearon, Kenneth C. H. ;
Argiles, Josep M. .
CLINICAL NUTRITION, 2007, 26 (05) :614-618
[8]  
Camussi G, 2011, AM J CANCER RES, V1, P98
[9]   Membrane Microvesicles as Actors in the Establishment of a Favorable Prostatic Tumoral Niche: A Role for Activated Fibroblasts and CX3CL1-CX3CR1 Axis [J].
Castellana, Donatello ;
Zobairi, Fatiha ;
Martinez, Maria Carmen ;
Panaro, Maria Antonietta ;
Mitolo, Vincenzo ;
Freyssinet, Jean-Marie ;
Kunzelmann, Corinne .
CANCER RESEARCH, 2009, 69 (03) :785-793
[10]   Causes and consequences of microRNA dysregulation in cancer [J].
Croce, Carlo M. .
NATURE REVIEWS GENETICS, 2009, 10 (10) :704-714