4.5 Article

Depleting Tumor-NQO1 Potentiates Anoikis and Inhibits Growth of NSCLC

Journal

MOLECULAR CANCER RESEARCH
Volume 14, Issue 1, Pages 14-25

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1541-7786.MCR-15-0207-T

Keywords

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Funding

  1. WV-CTSI [NIH-NIGMS U54 GM104942]
  2. ACS [IRG-09-061-04]
  3. NIH [CA102792-13]

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The fundamental role that NAD(P)H/quinone oxidoreductase 1 (NQO1) plays, in normal cells, as a cytoprotective enzyme guarding against stress induced by reactive oxygen species (ROS) is well documented. However, what is not known is whether the observed overexpression of NQO1 in neoplastic cells contributes to their survival. The current study discovered that depleting NQO1 expression in A549 and H292 lung adenocarcinoma cells caused an increase in ROS formation, inhibited anchorage-independent growth, increased anoikis sensitization, and decreased three-dimensional tumor spheroid invasion. These in vivo data further implicate tumor-NQO1 expression in a protumor survival role, because its depletion suppressed cell proliferation and decreased lung tumor xenograft growth. Finally, these data reveal an exploitable link between tumor-NQO1 expression and the survival of lung tumors because NQO1 depletion significantly decreased the percentage of ALDH((high)) cancer cells within the tumor population. (C)2015 AACR.

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