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Metabolic shifts toward glutamine regulate tumor growth, invasion and bioenergetics in ovarian cancer
Ist Teil von
Molecular systems biology, 2014-05, Vol.10 (5), p.728-n/a
Ort / Verlag
England: John Wiley & Sons, Inc
Erscheinungsjahr
2014
Link zum Volltext
Quelle
Wiley Online Library Journals
Beschreibungen/Notizen
Glutamine can play a critical role in cellular growth in multiple cancers. Glutamine‐addicted cancer cells are dependent on glutamine for viability, and their metabolism is reprogrammed for glutamine utilization through the tricarboxylic acid (TCA) cycle. Here, we have uncovered a missing link between cancer invasiveness and glutamine dependence. Using isotope tracer and bioenergetic analysis, we found that low‐invasive ovarian cancer (OVCA) cells are glutamine independent, whereas high‐invasive OVCA cells are markedly glutamine dependent. Consistent with our findings, OVCA patients’ microarray data suggest that glutaminolysis correlates with poor survival. Notably, the ratio of gene expression associated with glutamine anabolism versus catabolism has emerged as a novel biomarker for patient prognosis. Significantly, we found that glutamine regulates the activation of STAT3, a mediator of signaling pathways which regulates cancer hallmarks in invasive OVCA cells. Our findings suggest that a combined approach of targeting high‐invasive OVCA cells by blocking glutamine's entry into the TCA cycle, along with targeting low‐invasive OVCA cells by inhibiting glutamine synthesis and STAT3 may lead to potential therapeutic approaches for treating OVCAs.
Synopsis
Glutamine plays an important role in cellular growth in several cancers. In this study, a further link between glutamine dependency and tumor invasiveness is established in ovarian cancer. Glutamine maintains the high‐invasive phenotype by regulating STAT3 signaling.
High‐invasive ovarian cancer (OVCA) cells are glutamine dependent in contrast to low‐invasive cells that are glutamine independent.
Glutamine regulates STAT3 activation in high‐invasive cancer cells.
Glutamine's entry into TCA cycle modulates the invasive potential of high‐invasive cancer cells.
The ratio of glutamine catabolism over glutamine anabolism is associated with worse overall survival in OVCA patients.
Glutamine plays an important role in cellular growth in several cancers. In this study, a further link between glutamine dependency and tumor invasiveness is established in ovarian cancer. Glutamine maintains the high‐invasive phenotype by regulating STAT3 signaling.