15-LOX-1 suppression of hypoxia-induced metastatic phenotype and HIF-1α expression in human colon cancer cells

被引:26
作者
Wu, Yuanqing [1 ]
Mao, Fei [2 ]
Zuo, Xiangsheng [2 ]
Moussalli, Micheline J. [3 ]
Elias, Elias [2 ]
Xu, Weiguo [2 ]
Shureiqi, Imad [1 ,2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Clin Canc, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
15-Lipoxygenase-1; angiogenesis; HIF-1; alpha; hypoxia; ENDOTHELIAL-GROWTH-FACTOR; SUMO-SPECIFIC PROTEASE-1; HUMAN PROSTATE-CANCER; COLORECTAL-CANCER; 15-LIPOXYGENASE-1; EXPRESSION; INDUCIBLE FACTOR-1; DOWN-REGULATION; BREAST-CANCER; LINOLEIC-ACID; PPAR-GAMMA;
D O I
10.1002/cam4.222
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The expression of 15-lipoxygenase-1 (15-LOX-1) is downregulated in colon cancer and other major cancers, and 15-LOX-1 reexpression in cancer cells suppresses colonic tumorigenesis. Various lines of evidence indicate that 15-LOX-1 expression suppresses premetastatic stages of colonic tumorigenesis; nevertheless, the role of 15-LOX-1 loss of expression in cancer epithelial cells in metastases continues to be debated. Hypoxia, a common feature of the cancer microenvironment, promotes prometastatic mechanisms such as the upregulation of hypoxia-inducible factor (HIF)-1 alpha, a transcriptional master regulator that enhances cancer cell metastatic potential, angiogenesis, and tumor cell invasion and migration. We have, therefore, tested whether restoring 15-LOX-1 in colon cancer cells affects cancer cells' hypoxia response that promotes metastasis. We found that 15-LOX-1 reexpression in HCT116, HT29LMM, and LoVo colon cancer cells inhibited survival, vascular endothelial growth factor (VEGF) expression, angiogenesis, cancer cell migration and invasion, and HIF-1 alpha protein expression and stability under hypoxia. These findings demonstrate that 15-LOX-1 expression loss in cancer cells promotes metastasis and that therapeutically targeting ubiquitous 15-LOX-1 loss in cancer cells has the potential to suppress metastasis.
引用
收藏
页码:472 / 484
页数:13
相关论文
共 70 条
[1]  
BASTIDA E, 1991, INVAS METAST, V11, P273
[2]   Induction of the SUMO-specific protease 1 transcription by the androgen receptor in prostate cancer cells [J].
Bawa-Khalfe, Tasneem ;
Cheng, Jinke ;
Wang, Zhengxin ;
Yeh, Edward T. H. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (52) :37341-37349
[3]   SENP1 Induces Prostatic Intraepithelial Neoplasia through Multiple Mechanisms [J].
Bawa-Khalfe, Tasneem ;
Cheng, Jinke ;
Lin, Sue-Hwa ;
Ittmann, Michael M. ;
Yeh, Edward T. H. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (33) :25859-25866
[4]   Targeting hypoxic tumour cells to overcome metastasis [J].
Bennewith, Kevin L. ;
Dedhar, Shoukat .
BMC CANCER, 2011, 11
[5]   INTERLEUKIN 1-INDUCED CANCER CELL ENDOTHELIAL-CELL ADHESION INVITRO AND ITS RELATIONSHIP TO METASTASIS INVIVO - ROLE OF VESSEL WALL 13-HODE SYNTHESIS AND INTEGRIN EXPRESSION [J].
BERTOMEU, MC ;
GALLO, S ;
LAURI, D ;
HAAS, TA ;
ORR, FW ;
BASTIDA, E ;
BUCHANAN, MR .
CLINICAL & EXPERIMENTAL METASTASIS, 1993, 11 (03) :243-250
[6]   Endothelial Cell HIF-1α and HIF-2α Differentially Regulate Metastatic Success [J].
Branco-Price, Cristina ;
Zhang, Na ;
Schnelle, Moritz ;
Evans, Colin ;
Katschinski, Doerthe M. ;
Liao, Debbie ;
Ellies, Lesley ;
Johnson, Randall S. .
CANCER CELL, 2012, 21 (01) :52-65
[7]   Discovery of a second 15S-lipoxygenase in humans [J].
Brash, AR ;
Boeglin, WE ;
Chang, MS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (12) :6148-6152
[8]   Lipoxygenases: Occurrence, functions, catalysis, and acquisition of substrate [J].
Brash, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (34) :23679-23682
[9]  
Brizel DM, 1996, CANCER RES, V56, P941
[10]   Hypoxia Predicts Aggressive Growth and Spontaneous Metastasis Formation from Orthotopically Grown Primary Xenografts of Human Pancreatic Cancer [J].
Chang, Qing ;
Jurisica, Igor ;
Do, Trevor ;
Hedley, David W. .
CANCER RESEARCH, 2011, 71 (08) :3110-3120