Profilin-1 Overexpression in MDA-MB-231 Breast Cancer Cells Is Associated with Alterations in Proteomics Biomarkers of Cell Proliferation, Survival, and Motility as Revealed by Global Proteomics Analyses

被引:28
|
作者
Coumans, Joelle V. F. [1 ,2 ]
Gau, David [3 ]
Poljak, Anne [4 ,5 ]
Wasinger, Valerie [4 ,5 ]
Roy, Partha [3 ]
Moens, Pierre D. J. [1 ]
机构
[1] Univ New England, Sch Sci & Technol, Armidale, NSW 2351, Australia
[2] Univ New England, Sch Rural Med, Armidale, NSW 2351, Australia
[3] Univ Pittsburgh, Dept Bioengn & Pathol, Pittsburgh, PA USA
[4] Univ New S Wales, Mark Wainright Analyt Ctr, Bioanalyt Mass Spectrometry Facil, Sydney, NSW, Australia
[5] Univ New S Wales, Sch Med Sci, Sydney, NSW, Australia
关键词
MIGRATION INHIBITORY FACTOR; THIOREDOXIN REDUCTASE 1; HEAT-SHOCK PROTEINS; DUCTAL CARCINOMA; DOWN-REGULATION; APOPTOSIS; EXPRESSION; COFILIN; BINDING; CYCLE;
D O I
10.1089/omi.2014.0075
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Despite early screening programs and new therapeutic strategies, metastatic breast cancer is still the leading cause of cancer death in women in industrialized countries and regions. There is a need for novel biomarkers of susceptibility, progression, and therapeutic response. Global analyses or systems science approaches with omics technologies offer concrete ways forward in biomarker discovery for breast cancer. Previous studies have shown that expression of profilin-1 (PFN1), a ubiquitously expressed actin-binding protein, is downregulated in invasive and metastatic breast cancer. It has also been reported that PFN1 overexpression can suppress tumorigenic ability and motility/invasiveness of breast cancer cells. To obtain insights into the underlying molecular mechanisms of how elevating PFN1 level induces these phenotypic changes in breast cancer cells, we investigated the alteration in global protein expression profiles of breast cancer cells upon stable overexpression of PFN1 by a combination of three different proteome analysis methods (2-DE, iTRAQ, label-free). Using MDA-MB-231 as a model breast cancer cell line, we provide evidence that PFN1 overexpression is associated with alterations in the expression of proteins that have been functionally linked to cell proliferation (FKPB1A, HDGF, MIF, PRDX1, TXNRD1, LGALS1, STMN1, LASP1, S100A11, S100A6), survival (HSPE1, HSPB1, HSPD1, HSPA5 and PPIA, YWHAZ, CFL1, NME1) and motility (CFL1, CORO1B, PFN2, PLS3, FLNA, FLNB, NME2, ARHGDIB). In view of the pleotropic effects of PFN1 overexpression in breast cancer cells as suggested by these new findings, we propose that PFN1-induced phenotypic changes in cancer cells involve multiple mechanisms. Our data reported here might also offer innovative strategies for identification and validation of novel therapeutic targets and companion diagnostics for persons with, or susceptibility to, breast cancer.
引用
收藏
页码:778 / 791
页数:14
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