Potent Inhibitory Effect of δ-Tocopherol on Prostate Cancer Cells Cultured in Vitro and Grown As Xenograft Tumors in Vivo
Author(s) -
Huarong Huang,
Yan He,
Xiaoxing Cui,
Susan Goodin,
Hong Wang,
ChengFeng Du,
Dongli Li,
Kun Zhang,
AhNg Tony Kong,
Robert S. DiPaola,
Chung S. Yang,
Allan H. Conney,
Xi Zheng
Publication year - 2014
Publication title -
journal of agricultural and food chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.203
H-Index - 297
eISSN - 1520-5118
pISSN - 0021-8561
DOI - 10.1021/jf504058f
Subject(s) - prostate cancer , in vivo , apoptosis , cancer research , prostate , cancer , androgen receptor , in vitro , medicine , growth inhibition , cell growth , endocrinology , chemistry , biology , biochemistry , microbiology and biotechnology
In the present study, the effects of δ-tocopherol (δ-T) on growth and apoptosis of human prostate cancer cells were determined and compared with that of α-tocopherol (α-T), a commonly used form of vitamin E. Treatment of human prostate cancer cells with δ-T resulted in strong growth inhibition and apoptosis stimulation, while the effects of α-T were modest. The strong effects of δ-T on the cells were associated with suppression of androgen receptor (AR) activity and decreased level of prostate specific antigen (PSA) that is a downstream target of the AR signaling. In the in vivo study, we found that δ-T had a more potent inhibitory effect on the formation and growth of prostate xenograft tumors than that of α-T. Moreover, δ-T inhibited proliferation and stimulated apoptosis in the tumors. The present study identified δ-T as a better form of vitamin E than α-T for future clinical studies of prostate cancer prevention.
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