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Oncotarget

Osteopontin Induces Mitochondrial Biogenesis in Deadherent Cancer Cells

Dec 4, 2023
This podcast explores the relationship between Osteopontin splice variants and mitochondrial biogenesis in cancer cells, revealing a functional connection between short-term oxidative metabolism and long-term mitochondrial biogenesis, with potential implications for treating cancer metastasis.
02:33

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Quick takeaways

  • Osteopontin C, in conjunction with CD44-V, upregulates chloride-dependent cysteine glutamate transporter SLC7A11, leading to increased mitochondrial size.
  • Understanding the signaling pathways and mechanisms of mitochondrial biogenesis could lead to targeted therapies for reducing tumor mass in metastatic cancer.

Deep dives

Osteopontin Induces Mitochondrial Biogenesis in Cancer Metastasis

Researchers from the University of Cincinnati's James L. Winkle College of Pharmacy conducted a study to explore the connection between short-term oxidative metabolism and long-term mitochondrial biogenesis in cancer metastasis. The researchers hypothesized that Osteopontin splice variants, which increase ATP levels in dead heron cells, also stimulate mitochondrial growth through the same signaling mechanisms. Their study confirmed that Osteopontin C, in conjunction with the receptor CD44-V, upregulates the chloride-dependent cysteine glutamate transporter SLC7A11, leading to an increase in mitochondrial size. In vivo experiments showed that suppression of the biogenesis-inducing mechanisms reduced disseminated tumor mass, pointing to potential targets for treating cancer metastasis.

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