Isothermal Microcalorimetry of Tumor Cells: Enhanced Thermogenesis by Metastatic Cells.

Front Oncol

Laboratório de Bioquímica e Biologia Molecular Do Câncer, Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal Do Rio de Janeiro, Rio de Janeiro, Brazil.

Published: December 2019

AI Article Synopsis

  • Tumor cells, particularly metastatic ones, show altered metabolism, releasing more heat compared to non-metastatic cells, as analyzed through isothermal microcalorimetry.
  • In experiments, components such as mitochondrial extracts and inhibitors of actin filaments or specific genes influenced the heat release patterns of these cancer cells.
  • The presence of uncoupling protein 2 in metastatic cells and the impact of lipid metabolism on heat release suggest that this thermogenic activity could serve as a measurable indicator of cancer metastasis.

Article Abstract

Tumor cells exhibit rewired metabolism. We carried out comparative analyses attempting to investigate whether metabolic reprograming could be measured by isothermal microcalorimetry. Intact metastatic cell lines of tongue cell carcinoma, human and murine melanoma, lung, and breast tumors consistently released more heat than non-metastatic cells or cells displaying lower metastatic potential. In tongue squamous carcinoma cells mitochondrial enriched extract reproduced the heat release pattern of intact cells. Cytochalasin D, an actin filament inhibitor, and suppression of metastasis marker Melanoma associated gene 10 (MAGEA10) decreased heat release. Uncoupling protein 2 was highly expressed in metastatic cells, but not in non-metastatic cells. Carnitine palmitoyl transferase-1 inhibitor, Etomoxir strongly inhibited heat release by metastatic cells, thus linking lipid metabolism to thermogenesis. We propose that heat release may be a quantifiable trait of the metastatic process.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6930183PMC
http://dx.doi.org/10.3389/fonc.2019.01430DOI Listing

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