Format

Send to

Choose Destination
Mol Carcinog. 2016 May;55(5):420-30. doi: 10.1002/mc.22291. Epub 2015 Feb 3.

Elimination of ALDH+ breast tumor initiating cells by docosahexanoic acid and/or gamma tocotrienol through SHP-1 inhibition of Stat3 signaling.

Author information

1
Department of Nutritional Sciences, The University of Texas at Austin, Austin, Texas.
2
Department of Molecular Biosciences, The University of Texas at Austin, Austin, Texas.

Abstract

Study investigated the ability of docosahexaenoic acid (DHA) alone and in combination with gamma-tocotrienol (γT3) to eliminate aldehyde dehydrogenase positive (ALDH+) cells and to inhibit mammosphere formation, biomarker and functional assay for tumor initiating cells (TICs), respectively, in human triple negative breast cancer cells (TNBCs), and investigated possible mechanisms of action. DHA upregulated Src homology region 2 domain-containing protein tyrosine phosphatase-1 (SHP-1) protein levels and suppressed levels of phosphorylated signal transducer and activator of transcription-3 (pStat3) and its downstream mediators c-Myc, and cyclin D1. siRNA to SHP-1 enhanced the percentage of ALDH+ cells and Stat-3 signaling, as well as inhibited, in part, the ability of DHA to reduce the percentage of ALDH+ cells and Stat-3 signaling. γT3 alone and in combination with DHA reduced ALDH+ TNBCs, up-regulated SHP-1 protein levels, and suppressed Stat-3 signaling. Taken together, data demonstrate the anti-TIC potential of achievable concentrations of DHA alone as well as in combination with γT3.

KEYWORDS:

aldehyde dehydrogenase activity positive (ALDH+); cancer stem-like cells (CSCs); docosahexaenoic acid (DHA); gamma-tocotrienol (γT3); mammospheres; protein Src homology region 2 domain-containing tyrosine phosphatase (SHP-1); signal transducer and activator of transcription 3 (Stat-3); triple negative breast cancer (TNBC) cells; tumor initiating cells (TICs)

PMID:
25648304
DOI:
10.1002/mc.22291
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center