The extracellular matrix protein TGFBI induces microtubule stabilization and sensitizes ovarian cancers to paclitaxel

被引:196
作者
Ahmed, Ahmed Ashour [1 ,3 ,5 ]
Mills, Anthony D. [4 ]
Ibrahim, Ashraf E. K. [1 ]
Temple, Jillian [1 ,3 ]
Blenkiron, Cherie [3 ]
Vias, Maria [3 ]
Massie, Charlie E. [3 ]
Iyer, N. Gopalakrishna [3 ]
McGeoch, Adam [4 ]
Crawford, Robin [5 ]
Nicke, Barbara [6 ]
Downward, Julian [6 ]
Swanton, Charles [6 ]
Bell, Stephen D. [4 ]
Earl, Helena M. [3 ]
Laskey, Ronald A. [4 ]
Caldas, Carlos [2 ,3 ]
Brenton, James D. [1 ,3 ]
机构
[1] Li Ka Shing Ctr, Canc Res UK Cambridge Res Inst, Funct Genom Drug Resistance Lab, Cambridge CB2 0RE, England
[2] Li Ka Shing Ctr, Canc Res UK Cambridge Res Inst, Breast Canc Funct Genom Lab, Cambridge CB2 0RE, England
[3] Hutchison MRC Res Ctr, Dept Oncol, Cambridge CB2 0XZ, England
[4] Hutchison MRC Res Ctr, MRC Canc Cell Unit, Cambridge CB2 0XZ, England
[5] Cambridge Univ Hosp, NHS Fdn Trust, Addenbrookes Hosp, Gynaecol Oncol Reg Ctr, Cambridge CB2 0QQ, England
[6] Canc Res UK London Res Inst, Signal Transduct Lab, London WC2A 3PX, England
基金
英国医学研究理事会;
关键词
D O I
10.1016/j.ccr.2007.11.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The extracellular matrix (ECM) can induce chemotherapy resistance via AKT-mediated inhibition of apoptosis. Here, we show that loss of the ECM protein TGFBI (transforming growth factor beta induced) is sufficient to induce specific resistance to paclitaxel and mitotic spindle abnormalities in ovarian cancer cells. Paclitaxel-resistant cells treated with recombinant TGFBI protein show integrin-dependent restoration of paclitaxel sensitivity via FAK- and Rho-dependent stabilization of microtubules. Immunohistochemical staining for TGFBI in paclitaxel-treated ovarian cancers from a prospective clinical trial showed that morphological changes of paclitaxel-induced cytotoxicity were restricted to areas of strong expression of TGFBI. These data show that ECM can mediate taxane sensitivity by modulating microtubule stability.
引用
收藏
页码:514 / 527
页数:14
相关论文
共 57 条
[31]  
Mozzetti S, 2005, CLIN CANCER RES, V11, P298
[32]   A gene-expression signature to predict survival in breast cancer across independent data sets [J].
Naderi, A. ;
Teschendorff, A. E. ;
Barbosa-Morais, N. I. ;
Pinder, S. E. ;
Green, A. R. ;
Powe, D. G. ;
Robertson, J. F. R. ;
Aparicio, S. ;
Ellis, I. O. ;
Brenton, J. D. ;
Caldas, C. .
ONCOGENE, 2007, 26 (10) :1507-1516
[33]   Identification of the αvβ3 integrin-interacting motif of βig-h3 and its anti-angiogenic effect [J].
Nam, JO ;
Kim, JE ;
Jeong, HW ;
Lee, SJ ;
Lee, BH ;
Choi, JY ;
Park, RW ;
Park, JY ;
Kim, IS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (28) :25902-25909
[34]   How cells get the right chromosomes [J].
Nicklas, RB .
SCIENCE, 1997, 275 (5300) :632-637
[35]   Localized stabilization of microtubules by integrin- and FAK-facilitated Rho signaling [J].
Palazzo, AF ;
Eng, CH ;
Schlaepfer, DD ;
Marcantonio, EE ;
Gundersen, GG .
SCIENCE, 2004, 303 (5659) :836-839
[36]   Beta ig-h3 promotes renal proximal tubular epithelial cell adhesion, migration and proliferation through the interaction with α3β1 integrin [J].
Park, SW ;
Bae, JS ;
Kim, KS ;
Park, SH ;
Lee, BH ;
Choi, JY ;
Park, JY ;
Ha, SW ;
Kim, YL ;
Kwon, TH ;
Kim, IS ;
Park, RW .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2004, 36 (03) :211-219
[37]  
Parmar MKB, 2002, LANCET, V360, P505
[38]   Fluoxetine inhibits multidrug resistance extrusion pumps and enhances responses to chemotherapy in syngeneic and in human xenograft mouse tumor models [J].
Peer, D ;
Dekel, Y ;
Melikhov, D ;
Margalit, R .
CANCER RESEARCH, 2004, 64 (20) :7562-7569
[39]   Paclitaxel-carboplatin alone or with bevacizumab for non-small-cell lung cancer [J].
Sandler, Alan ;
Gray, Robert ;
Perry, Michael C. ;
Brahmer, Julie ;
Schiller, Joan H. ;
Dowlati, Afshin ;
Lilenbaum, Rogerio ;
Johnson, David H. .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (24) :2542-2550
[40]   Mitotic phosphorylation of Bcl-2 during normal cell cycle progression and taxol-induced growth arrest [J].
Scatena, CD ;
Stewart, ZA ;
Mays, D ;
Tang, LJ ;
Keefer, CJ ;
Leach, SD ;
Pietenpol, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (46) :30777-30784