2017-01-16T10:47:14Z
2017-01-16T10:47:14Z
2016-04-05
2017-01-05T09:14:02Z
The mechanisms that allow breast cancer (BCa) cells to metabolically sustain rapid growth are poorly understood. Here we report that BCa cells are dependent on a mechanism to supply precursors for intracellular lipid production derived from extracellular sources and that the endothelial lipase (LIPG) fulfils this function. LIPG expression allows the import of lipid precursors, thereby contributing to BCa proliferation. LIPG stands out as an essential component of the lipid metabolic adaptations that BCa cells, and not normal tissue, must undergo to support high proliferation rates. LIPG is ubiquitously and highly expressed under the control of FoxA1 or FoxA2 in all BCa subtypes. The downregulation of either LIPG or FoxA in transformed cells results in decreased proliferation and impaired synthesis of intracellular lipids.
Article
Published version
English
Càncer de mama; Hidrolases; Biologia molecular; Factors de transcripció; Breast cancer; Hydrolases; Molecular biology; Transcription factors
Macmillan
Reproducció del document publicat a: http://dx.doi.org/10.1038/ncomms11199
Nature Communications, 2016, vol. 7, num. 11199
http://dx.doi.org/10.1038/ncomms11199
cc by (c) Slebe et al., 2016
http://creativecommons.org/licenses/by/3.0/es/