PURPOSE: The expression of survivin, a member of the inhibitor-of-apoptosis protein family, is elevated in many types of human cancer. High survivin expression has been associated with poor patient prognosis and tumor resistance to chemotherapy and radiotherapy. The purpose of this study was to compare the radiosensitizing effects of five agents that target survivin on their relative ability to downregulate survivin expression. METHODS AND MATERIALS: The human epidermoid carcinoma cell line A431 was treated with adenoviral-mediated wild-type p53, antisense to survivin, the mitogen-activated protein kinase inhibitor PD98059, the cyclin-dependent kinase inhibitor Purvalanol A, or the histone deacetylase inhibitor trichostatin A. The radiosensitizing effects of these treatments were determined by clonogenic survival curve analysis and their abilities to suppress survivin expression by Western blot analysis. RESULTS: All the strategies were shown to radiosensitize A431 cells. This effect correlated with their abilities to downregulate survivin. CONCLUSION: Expression of survivin appears to confer a radioresistant phenotype that can be overcome using several clinically achievable strategies that target survivin either specifically or nonspecifically.
PURPOSE: The expression of survivin, a member of the inhibitor-of-apoptosis protein family, is elevated in many types of humancancer. High survivin expression has been associated with poor patient prognosis and tumor resistance to chemotherapy and radiotherapy. The purpose of this study was to compare the radiosensitizing effects of five agents that target survivin on their relative ability to downregulate survivin expression. METHODS AND MATERIALS: The humanepidermoid carcinoma cell line A431 was treated with adenoviral-mediated wild-type p53, antisense to survivin, the mitogen-activated protein kinase inhibitor PD98059, the cyclin-dependent kinase inhibitor Purvalanol A, or the histone deacetylase inhibitor trichostatin A. The radiosensitizing effects of these treatments were determined by clonogenic survival curve analysis and their abilities to suppress survivin expression by Western blot analysis. RESULTS: All the strategies were shown to radiosensitize A431 cells. This effect correlated with their abilities to downregulate survivin. CONCLUSION: Expression of survivin appears to confer a radioresistant phenotype that can be overcome using several clinically achievable strategies that target survivin either specifically or nonspecifically.
Authors: David J Grdina; Jeffrey S Murley; Richard C Miller; Helena J Mauceri; Harold G Sutton; Jian Jian Li; Gayle E Woloschak; Ralph R Weichselbaum Journal: Cancer Res Date: 2013-05-07 Impact factor: 12.701
Authors: T Iwasa; I Okamoto; K Takezawa; K Yamanaka; T Nakahara; A Kita; H Koutoku; M Sasamata; E Hatashita; Y Yamada; K Kuwata; M Fukuoka; K Nakagawa Journal: Br J Cancer Date: 2010-06-01 Impact factor: 9.075