Rac1/Pak1/p38/MMP-2 Axis Regulates Angiogenesis in Ovarian Cancer

被引:66
作者
Gonzalez-Villasana, Vianey [1 ]
Fuentes-Mattei, Enrique [2 ]
Ivan, Cristina [3 ]
Dalton, Heather J. [4 ]
Rodriguez-Aguayo, Cristian [1 ]
Fernandez-de Thomas, Ricardo J. [1 ]
Aslan, Burcu [1 ]
Monroig, Paloma del C. [1 ,5 ]
Velazquez-Torres, Guermarie [2 ]
Previs, Rebecca A. [3 ]
Pradeep, Sunila [3 ]
Kahraman, Nermin [1 ]
Wang, Huamin [6 ]
Kanlikilicer, Pinar [1 ]
Ozpolat, Bulent [1 ]
Calin, George [1 ,7 ]
Sood, Anil K. [3 ,4 ,7 ]
Lopez-Berestein, Gabriel [1 ,7 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77054 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Houston, TX 77054 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Canc Biol, Houston, TX 77054 USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Gynecol Oncol, Houston, TX 77054 USA
[5] Univ Puerto Rico, Sch Med, San Juan, PR 00936 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77054 USA
[7] Univ Texas MD Anderson Canc Ctr, Ctr RNAi & Noncoding RNA, Houston, TX 77054 USA
关键词
MATRIX METALLOPROTEINASES; ZOLEDRONIC ACID; IN-VITRO; BISPHOSPHONATES INHIBIT; BREAST-CANCER; CELL-DEATH; P38; KINASE; RAC1; TARGET;
D O I
10.1158/1078-0432.CCR-14-2279
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Zoledronic acid is being increasingly recognized for its antitumor properties, but the underlying functions are not well understood. In this study, we hypothesized that zoledronic acid inhibits ovarian cancer angiogenesis preventing Rac1 activation. Experimental Design: The biologic effects of zoledronic acid were examined using a series of in vitro [cell invasion, cytokine production, Rac1 activation, reverse-phase protein array, and in vivo (orthotopic mouse models)] experiments. Results: There was significant inhibition of ovarian cancer (HeyA8-MDR and OVCAR-5) cell invasion as well as reduced production of proangiogenic cytokines in response to zoledronic acid treatment. Furthermore, zoledronic acid inactivated Rac1 and decreased the levels of Pak1/p38/matrix metalloproteinase-2 in ovarian cancer cells. In vivo, zoledronic acid reduced tumor growth, angiogenesis, and cell proliferation and inactivated Rac1 in both HeyA8-MDR and OVCAR-5 models. These in vivo antitumor effects were enhanced in both models when zoledronic acid was combined with nab-paclitaxel. Conclusions: Zoledronic acid has robust antitumor and anti-angiogenic activity and merits further clinical development as ovarian cancer treatment. (C) 2015 AACR.
引用
收藏
页码:2127 / 2137
页数:11
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