Long-Chain Fatty Acid Analogues Suppress Breast Tumorigenesis and Progression

被引:33
作者
Gluschnaider, Udi [1 ]
Hertz, Rachel [1 ]
Ohayon, Sarit [1 ]
Smeir, Elia [1 ]
Smets, Martha [1 ]
Pikarsky, Eli [2 ]
Bar-Tana, Jacob [1 ]
机构
[1] Hebrew Univ Jerusalem, Sch Med, Dept Human Nutr & Metab, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Sch Med, Dept Pathol, IL-91120 Jerusalem, Israel
关键词
FULL NEOPLASTIC TRANSFORMATION; PROTEIN-TYROSINE KINASES; LARGE TUMOR-ANTIGEN; IN-VIVO; OXIDATIVE STRESS; CARCINOMA CELLS; ACYL ANALOGS; MEDICA; 16; CANCER; SRC;
D O I
10.1158/0008-5472.CAN-14-0385
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Obesity and type 2 diabetes (T2D) are associated with increased breast cancer incidence and mortality, whereas carbohydrate-restricted ketogenic diets ameliorate T2D and suppress breast cancer. These observations suggest an inherent efficacy of nonesterified long-chain fatty acids (LCFA) in suppressing T2D and breast tumorigenesis. In this study, we investigated novel antidiabetic MEDICA analogues consisting of methyl-substituted LCFA that are neither beta-oxidized nor esterified to generate lipids, prompting interest in their potential efficacy as antitumor agents in the context of breast cancer. In the MMTV-PyMT oncomouse model of breast cancer, in which we confirmed that tumor growth could be suppressed by a carbohydrate-restricted ketogenic diet, MEDICA treatment suppressed tumor growth, and lung metastasis, promoting a differentiated phenotype while suppressing mesenchymal markers. In human breast cancer cells, MEDICA treatment attenuated signaling through the STAT3 and c-Src transduction pathways. Mechanistic investigations suggested that MEDICA suppressed c-Src-transforming activity by elevating reactive oxygen species production, resulting in c-Src oxidation and oligomerization. Our findings suggest that MEDICA analogues may offer therapeutic potential in breast cancer and overcome the poor compliance of patients to dietary carbohydrate restriction. (C) 2014 AACR.
引用
收藏
页码:6991 / 7002
页数:12
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共 50 条
[1]   Ketogenic Diets Enhance Oxidative Stress and Radio-Chemo-Therapy Responses in Lung Cancer Xenografts [J].
Allen, Bryan G. ;
Bhatia, Sudershan K. ;
Buatti, John M. ;
Brandt, Kristin E. ;
Lindholm, Kaleigh E. ;
Button, Anna M. ;
Szweda, Luke I. ;
Smith, Brian J. ;
Spitz, Douglas R. ;
Fath, Melissa A. .
CLINICAL CANCER RESEARCH, 2013, 19 (14) :3905-3913
[2]  
Arulanandam R, 2010, ANTICANCER RES, V30, P47
[3]  
BARTANA J, 1988, J LIPID RES, V29, P431
[4]   SYNTHESIS AND HYPOLIPIDEMIC AND ANTIDIABETOGENIC ACTIVITIES OF BETA,BETA,BETA',BETA'-TETRASUBSTITUTED, LONG-CHAIN DIOIC ACIDS [J].
BARTANA, J ;
BENSHOSHAN, S ;
BLUM, J ;
MIGRON, Y ;
HERTZ, R ;
PILL, J ;
ROSEKHAN, G ;
WITTE, EC .
JOURNAL OF MEDICINAL CHEMISTRY, 1989, 32 (09) :2072-2084
[5]   Simultaneous siRNA Targeting of Src and Downstream Signaling Molecules Inhibit Tumor Formation and Metastasis of a Human Model Breast Cancer Cell Line [J].
Bjorge, Jeffrey D. ;
Pang, Andy S. ;
Funnell, Melanie ;
Chen, Ke Yun ;
Diaz, Roman ;
Magliocco, Anthony M. ;
Fujita, Donald J. .
PLOS ONE, 2011, 6 (04)
[6]   Syngeneic mouse mammary carcinoma cell lines: Two closely related cell lines with divergent metastatic behavior [J].
Borowsky, AD ;
Namba, R ;
Young, LJT ;
Hunter, KW ;
Hodgson, JG ;
Tepper, CG ;
McGoldrick, ET ;
Muller, WJ ;
Cardiff, R ;
Gregg, JP .
CLINICAL & EXPERIMENTAL METASTASIS, 2005, 22 (01) :47-58
[7]   Stat3 activation is required for cellular transformation by v-src [J].
Bromberg, JF ;
Horvath, CM ;
Besser, D ;
Lathem, WW ;
Darnell, JE .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (05) :2553-2558
[8]   Quantitative In vivo Imaging of the Effects of Inhibiting Integrin Signaling via Src and FAK on Cancer Cell Movement: Effects on E-cadherin Dynamics [J].
Canel, Marta ;
Serrels, Alan ;
Miller, Derek ;
Timpson, Paul ;
Serrels, Bryan ;
Frame, Margaret C. ;
Brunton, Valerie G. .
CANCER RESEARCH, 2010, 70 (22) :9413-9422
[9]   Inhibition of Src Family Kinases and Receptor Tyrosine Kinases by Dasatinib: Possible Combinations in Solid Tumors [J].
Carlos Montero, Juan ;
Seoane, Samuel ;
Ocana, Alberto ;
Pandiella, Atanasio .
CLINICAL CANCER RESEARCH, 2011, 17 (17) :5546-5552
[10]   CARBOXY TERMINUS OF POLYOMA MIDDLE-SIZED TUMOR-ANTIGEN IS REQUIRED FOR ATTACHMENT TO MEMBRANES, ASSOCIATED PROTEIN-KINASE ACTIVITIES, AND CELL-TRANSFORMATION [J].
CARMICHAEL, GG ;
SCHAFFHAUSEN, BS ;
DORSKY, DI ;
OLIVER, DB ;
BENJAMIN, TL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (11) :3579-3583