Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3999356 | Urologic Oncology: Seminars and Original Investigations | 2016 | 8 Pages |
Abstract
Our results indicate that KLF5 is an essential transcription regulator of MKK7 kinase and promotes the apoptosis induced by TNFα in LNCaP cells. Loss of KLF5 in prostate cancer may decrease cell response to TNFα-inducing apoptosis and facilitate cancer initiation and progression; moreover, KLF5 could be a potential molecular marker for predicting the effect of high-dose TNFα on tumor growth inhibition in prostate cancer.
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Authors
Qi Ph.D., Yang Ph.D., Shan M.S., Chong M.S., Feng Ph.D., Xiao-Shuang Ph.D., Jing Ph.D., Xinyang A.S., Luke M.D., Dalin M.D., Peng Ph.D.,