β1 integrin as a molecular therapeutic target

被引:54
作者
Cordes, Nils
Park, Catherine C.
机构
[1] Tech Univ Dresden, Med Fac Carl Gustav Carus, OncoRay Ctr Radiat Res Oncol, D-01307 Dresden, Germany
[2] Univ Calif San Francisco, Dept Radiat Oncol, San Francisco, CA 94143 USA
关键词
beta1; integrin; ionizing radiation; radiotherapy; tumor;
D O I
10.1080/09553000701639694
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Purpose: Radiation therapy ( RT) is a commonly used modality to treat human cancer. However, dose-limiting toxicity and resistance are major problems to improving treatment efficacy. Increasing evidence has pointed to the critical role of the tumor microenvironment and cell-extracellular matrix ( ECM), specifically via beta 1 integrins, in modifying response to therapy, including radiation. beta 1 integrins have been implicated in several key processes in malignant progression and metastasis, and more recently in mediating resistance to cytotoxic chemotherapy and radiation. Evidence is mounting that beta 1 integrins mediate essential survival signals post-IR, through both canonical and non-canonical integrin signaling pathways that make it a highly promising therapeutic target for several solid malignancies. Conclusions: In this mini-review article, we briefly summarize the most recent emerging findings concerning beta 1 integrin and radiation survival that indicate the promise of beta 1 integrin inhibitory agents as radiosensitizers.
引用
收藏
页码:753 / 760
页数:8
相关论文
共 72 条
[1]   Myoepithelial cells: good fences make good neighbors [J].
Adriance, MC ;
Inman, JL ;
Petersen, OW ;
Bissell, MJ .
BREAST CANCER RESEARCH, 2005, 7 (05) :190-197
[2]   Integrin signaling inhibits paclitaxel-induced apoptosis in breast cancer cells [J].
Aoudjit, F ;
Vuori, K .
ONCOGENE, 2001, 20 (36) :4995-5004
[3]   Radiation and the microenvironment - Tumorigenesis and therapy [J].
Barcellos-Hoff, MH ;
Park, C ;
Wright, EG .
NATURE REVIEWS CANCER, 2005, 5 (11) :867-875
[4]  
BARCELLOSHOFF MH, 1993, CANCER RES, V53, P3880
[5]   Selective inhibition of the epidermal growth factor receptor tyrosine kinase by BIBX1382BS and the improvement of growth delay, but not local control, after fractionated irradiation in human FaDu squamous cell carcinoma in the nude mouse [J].
Baumann, M ;
Krause, M ;
Zips, D ;
Eicheler, W ;
Dörfler, A ;
Ahrens, J ;
Petersen, C ;
Brüchner, K ;
Hilberg, F .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 2003, 79 (07) :547-559
[6]   Integrin expression and survival in human breast cancer [J].
Berry, MG ;
Gui, GPH ;
Wells, CA ;
Carpenter, R .
EJSO, 2004, 30 (05) :484-489
[7]  
Bissell MJ, 1999, CANCER RES, V59, p1757S
[8]   Radiotherapy plus cetuximab for squamous-cell carcinoma of the head and neck [J].
Bonner, JA ;
Harari, PM ;
Giralt, J ;
Azarnia, N ;
Shin, DM ;
Cohen, RB ;
Jones, CU ;
Sur, R ;
Raben, D ;
Jassem, J ;
Ove, R ;
Kies, MS ;
Baselga, J ;
Youssoufian, H ;
Amellal, N ;
Rowinsky, EK ;
Ang, KK .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 354 (06) :567-578
[9]   A NEW DIPLOID NONTUMORIGENIC HUMAN-BREAST EPITHELIAL-CELL LINE ISOLATED AND PROPAGATED IN CHEMICALLY DEFINED MEDIUM [J].
BRIAND, P ;
PETERSEN, OW ;
VANDEURS, B .
IN VITRO CELLULAR & DEVELOPMENTAL BIOLOGY, 1987, 23 (03) :181-188
[10]   Radiation-enhanced hepatocellular carcinoma cell invasion with MMP-9 expression through PI3K/Akt/NF-κB signal transduction pathway [J].
Cheng, J. C-H ;
Chou, C. H. ;
Kuo, M. L. ;
Hsieh, C-Y .
ONCOGENE, 2006, 25 (53) :7009-7018