A neuronal network of mitochondrial dynamics regulates metastasis.
M Cecilia CainoJae Ho SeoAngeline AguinaldoEric WaitKelly G BryantAndrew V KossenkovJames E HaydenValentina VairaAnnamaria MorottiStefano FerreroSilvano BosariDmitry I GabrilovichLucia R LanguinoAndrew R CohenDario C AltieriPublished in: Nature communications (2016)
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.
Keyphrases
- oxidative stress
- papillary thyroid
- genome wide
- cell death
- squamous cell carcinoma
- reactive oxygen species
- squamous cell
- small cell lung cancer
- signaling pathway
- dna methylation
- spinal cord
- cell proliferation
- case report
- spinal cord injury
- high throughput
- blood brain barrier
- gene expression
- childhood cancer
- mesenchymal stem cells
- brain injury
- copy number