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A neuronal network of mitochondrial dynamics regulates metastasis

The role of mitochondria in cancer is controversial. Using a genome-wide shRNA screen, we now show that tumours reprogram a network of mitochondrial dynamics operative in neurons, including syntaphilin (SNPH), kinesin KIF5B and GTPase Miro1/2 to localize mitochondria to the cortical cytoskeleton and...

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Detalles Bibliográficos
Autores principales: Caino, M. Cecilia, Seo, Jae Ho, Aguinaldo, Angeline, Wait, Eric, Bryant, Kelly G., Kossenkov, Andrew V., Hayden, James E., Vaira, Valentina, Morotti, Annamaria, Ferrero, Stefano, Bosari, Silvano, Gabrilovich, Dmitry I., Languino, Lucia R., Cohen, Andrew R., Altieri, Dario C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5187409/
https://www.ncbi.nlm.nih.gov/pubmed/27991488
http://dx.doi.org/10.1038/ncomms13730
Descripción
Sumario:The role of mitochondria in cancer is controversial. Using a genome-wide shRNA screen, we now show that tumours reprogram a network of mitochondrial dynamics operative in neurons, including syntaphilin (SNPH), kinesin KIF5B and GTPase Miro1/2 to localize mitochondria to the cortical cytoskeleton and power the membrane machinery of cell movements. When expressed in tumours, SNPH inhibits the speed and distance travelled by individual mitochondria, suppresses organelle dynamics, and blocks chemotaxis and metastasis, in vivo. Tumour progression in humans is associated with downregulation or loss of SNPH, which correlates with shortened patient survival, increased mitochondrial trafficking to the cortical cytoskeleton, greater membrane dynamics and heightened cell invasion. Therefore, a SNPH network regulates metastatic competence and may provide a therapeutic target in cancer.