Celecoxib-Induced Cytotoxic Effect Is Potentiated by Inhibition of Autophagy in Human Urothelial Carcinoma Cells

نویسندگان

  • Kuo-How Huang
  • Kuan-Lin Kuo
  • I-Lin Ho
  • Hong-Chiang Chang
  • Yuan-Ting Chuang
  • Wei-Chou Lin
  • Ping-Yi Lee
  • Shih-Chen Chang
  • Chih-Kang Chiang
  • Yeong-Shiau Pu
  • Chien-Tso Chou
  • Chen-Hsun Hsu
  • Shing-Hwa Liu
چکیده

Celecoxib, a cyclooxygenase-2 (COX-2) inhibitor, can elicit anti-tumor effects in various malignancies. Here, we sought to clarify the role of autophagy in celecoxib-induced cytotoxicity in human urothelial carcinoma (UC) cells. The results shows celecoxib induced cellular stress response such as endoplasmic reticulum (ER) stress, phosopho-SAPK/JNK, and phosopho-c-Jun as well as autophagosome formation in UC cells. Inhibition of autophagy by 3-methyladenine (3-MA), bafilomycin A1 or ATG7 knockdown potentiated celecoxib-induced apoptosis. Up-regulation of autophagy by rapamycin or GFP-LC3B-transfection alleviated celecoxib-induced cytotoxicity in UC cells. Taken together, the inhibition of autophagy enhances therapeutic efficacy of celecoxib in UC cells, suggesting a novel therapeutic strategy against UC.

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عنوان ژورنال:

دوره 8  شماره 

صفحات  -

تاریخ انتشار 2013