Abstract 965: The KISS1 metastasis suppressor appears to reverse the ‘Warburg Effect’

In 1924, Otto Warburg described the preference of cancer cells for glycolytic metabolism, even under normoxic conditions and that these metabolic changes directly correlate with malignant potential of several cancers. Although its purpose remains unclear, the “Warburg Effect” is thought to confer pr...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2011-04, Vol.71 (8_Supplement), p.965-965
Hauptverfasser: Welch, Danny R., Beck, Benjamin H., Feeley, Kyle P., Diers, Anne R., Vaidya, Kedar S., Nash, Kevin T., Bodenstine, Thomas M., Thomas, John W., Landar, Aimee, Ballinger, Scott W.
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Sprache:eng
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Zusammenfassung:In 1924, Otto Warburg described the preference of cancer cells for glycolytic metabolism, even under normoxic conditions and that these metabolic changes directly correlate with malignant potential of several cancers. Although its purpose remains unclear, the “Warburg Effect” is thought to confer proliferative and survival advantages by increasing uptake of nutrients into biomass. The KISS1 metastasis suppressor protein is secreted and proteolytically cleaved into so-called kisspeptins (KP) that block the colonization of metastatic C8161.9 human melanoma cells at secondary sites. We asked whether secreted KISS1 mediates its inhibitory effects on metastatic growth through regulation of the “Warburg Effect.” Comparing multiple bioenergetic and metabolic aspects of glucose metabolism in C8161.9 ± KISS1 showed that all KISS1-secreting clones had significantly (P
ISSN:0008-5472
1538-7445
DOI:10.1158/1538-7445.AM2011-965