resveratrol enhances antitumor activity of trail in prostate cancer xenografts through activation of foxo transcription factor白藜芦醇增强抗肿瘤活性的小道在前列腺癌异种移植foxo转录因子的激活.pdfVIP
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resveratrol enhances antitumor activity of trail in prostate cancer xenografts through activation of foxo transcription factor白藜芦醇增强抗肿瘤活性的小道在前列腺癌异种移植foxo转录因子的激活
Resveratrol Enhances Antitumor Activity of TRAIL in
Prostate Cancer Xenografts through Activation of FOXO
Transcription Factor
1 2 3 4 5
Suthakar Ganapathy , Qinghe Chen , Karan P. Singh , Sharmila Shankar , Rakesh K. Srivastava *
1 Division of Radiation Biology, Department of Radiation Oncology, The University of Texas Health Science Center at San Antonio, Greehey Children’s Cancer Research
Institute, San Antonio, Texas, United States of America, 2 Virginia Bioinformatics Institute, Virginia Polytechnic Institute and State University, Blacksburg, Virginia, United
States of America, 3 Department of Biostatistics, University of North Texas Health Science Center at Fort Worth, Fort Worth, Texas, United States of America, 4 Department
of Pathology and Laboratory Medicine, The University of Kansas Cancer Center, The University of Kansas Medical Center, Kansas City, Kansas, United States of America,
5 Department of Pharmacology, Toxicology and Therapeutics, and Medicine, The University of Kansas Cancer Center, The University of Kansas Medical Center, Kansas City,
Kansas, United States of America
Abstract
Background: Resveratrol (3, 49, 5 tri-hydroxystilbene), a naturally occurring polyphenol, exhibits anti-inflammatory,
antioxidant, cardioprotective and antitumor activities. We have recently shown that resveratrol can enhance the apoptosis-
inducing potential of TRAIL in prostate cancer cells through multiple mechanisms in vitro. Therefore, the present study was
designed to validate whether resveratrol can enhance the apoptosis-inducing potential of TRAIL in a xenograft model of
prostate cancer.
Methodology/Principal Findings: Resveratrol and TRAIL alone inhibited growth of PC-3 xenografts in nude mice by
inhibiting
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