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
相关论文
共 50 条
  • [21] Interaction of two metastasis suppressors, Nm23-H1 and Gelsolin, in the proliferation and motility of MDA-MB-231 breast carcinoma cells
    Marino, Natascia
    Marshall, Jean-Claude A.
    Collins, Joshua
    Zhou, Ming
    Veenstra, Timothy
    Steeg, Patricia S.
    [J]. CANCER RESEARCH, 2012, 72
  • [22] Cell proliferation inhibitory and apoptosis-inducing properties of anacardic acid and lunasin in human breast cancer MDA-MB-231 cells
    Hsieh, Chia-Chien
    Hernandez-Ledesma, Blanca
    de Lumen, Ben O.
    [J]. FOOD CHEMISTRY, 2011, 125 (02) : 630 - 636
  • [23] Urokinase is a Negative Modulator of Egf-dependent Proliferation and Motility in the Two Breast Cancer Cell Lines MCF-7 and MDA-MB-231
    Kozlova, Nina
    Samoylenko, Anatoly
    Drobot, Lyudmyla
    Kietzmann, Thomas
    [J]. MOLECULAR CARCINOGENESIS, 2016, 55 (02) : 170 - 181
  • [24] Urokinase modulates EGF-dependent signalling, proliferation and motility of the two breast cancer cell lines MCF-7 and MDA-MB-231
    Kozlova, N.
    Samoylenko, A.
    Drobot, L.
    Kietzmann, T.
    [J]. EUROPEAN JOURNAL OF CANCER, 2014, 50 : S123 - S123
  • [25] Downregulation of GATS gene inhibits proliferation, clonogenicity and migration in triple negative breast cancer cells MDA-MB-231 by cell autophagy
    Feng, Fan
    Zhang, Dongjing
    Han, Fangkai
    Zhang, Xingtao
    Duan, Tengfei
    Zhang, Xiuwen
    [J]. CANCER BIOMARKERS, 2019, 26 (03) : 261 - 269
  • [26] Therapeutic effects of hAMSCs secretome on proliferation of MDA-MB-231 breast cancer cells by the cell cycle arrest in G1/S phase
    Marzieh Rahimi Lifshagerd
    Fatemeh Safari
    [J]. Clinical and Translational Oncology, 2023, 25 : 1702 - 1709
  • [27] Invasive Breast Cancer: miR-24-2 Targets Genes Associated with Survival and Sensitizes MDA-MB-231 Cells to Berberine
    Ali, Mansoor
    Bamezai, Rameshwar N. K.
    Singh, Rana P.
    [J]. OMICS-A JOURNAL OF INTEGRATIVE BIOLOGY, 2023, 27 (09) : 409 - 420
  • [28] Therapeutic effects of hAMSCs secretome on proliferation of MDA-MB-231 breast cancer cells by the cell cycle arrest in G1/S phase
    Lifshagerd, Marzieh Rahimi
    Safari, Fatemeh
    [J]. CLINICAL & TRANSLATIONAL ONCOLOGY, 2023, 25 (06): : 1702 - 1709
  • [29] The suppression of cell motility through the reduction of FAK activity and expression of cell adhesion proteins by hAMSCs secretome in MDA-MB-231 breast cancer cells
    Safari, Fatemeh
    Bararpour, Setareh
    Chomachaei, Fatemeh Omidi
    [J]. INVESTIGATIONAL NEW DRUGS, 2024, 42 (03) : 272 - 280
  • [30] Brefeldin A Reduces Anchorage-Independent Survival, Cancer Stem Cell Potential and Migration of MDA-MB-231 Human Breast Cancer Cells
    Tseng, Chao-Neng
    Hong, Yi-Ren
    Chang, Hsueh-Wei
    Yu, Tsai-Jung
    Hung, Ting-Wei
    Hou, Ming-Feng
    Yuan, Shyng-Shiou F.
    Cho, Chung-Lung
    Liu, Chien-Tsung
    Chiu, Chien-Chih
    Huang, Chih-Jen
    [J]. MOLECULES, 2014, 19 (11) : 17464 - 17477