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Betulinic acid induces apoptosis of gallbladder cancer cells via repressing SCD1.
Wang, Hongfei; Dong, Fangxiao; Wang, Ye; Wang, Xu'an; Hong, Defei; Liu, Yingbin; Zhou, Jian.
Affiliation
  • Wang H; Department of General Surgery, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China.
  • Dong F; Shanghai Key Laboratory of Biliary Tract Disease Research, Shanghai 200092, China.
  • Wang Y; Department of Model Animal Research, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China.
  • Wang X; Department of Model Animal Research, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China.
  • Hong D; Department of General Surgery, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China.
  • Liu Y; Shanghai Key Laboratory of Biliary Tract Disease Research, Shanghai 200092, China.
  • Zhou J; Department of General Surgery, Sir Run Run Shaw Hospital Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou 310016, China.
Acta Biochim Biophys Sin (Shanghai) ; 52(2): 200-206, 2020 Feb 03.
Article in En | MEDLINE | ID: mdl-31915810
ABSTRACT
Gallbladder cancer (GBC) is the most common and aggressive malignancy of the biliary tract. Betulinic acid (BetA) has been reported to have anti-inflammatory and antitumor effects; however, the effect of BetA on GBC is still unknown. In this study, we investigated the effect of BetA on five GBC cell lines and found that BetA significantly inhibited the proliferation of NOZ cells but had little inhibitory effect on other GBC cells. BetA disturbed mitochondrial membrane potential and induced apoptosis in NOZ cells. Real-time polymerase chain reaction analysis revealed that stearoyl-coenzyme A desaturase 1 (SCD1) was highly expressed in NOZ cells but low expressed in other GBC cells. BetA inhibited SCD1 expression in a concentration-dependent manner in NOZ cells. Downregulation of SCD1 expression by RNA interference inhibited the proliferation of NOZ cells and induced cell apoptosis. Moreover, BetA inhibited the growth of xenografted tumors and suppressed SCD1 expression in nude mice. Thus, our results showed that BetA induced apoptosis through repressing SCD1 expression in GBC, suggesting that BetA might be an effective agent for the treatment of patients with GBC that highly expresses SCD1.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stearoyl-CoA Desaturase / Triterpenes / Apoptosis / Gallbladder Neoplasms Limits: Animals / Humans Language: En Journal: Acta Biochim Biophys Sin (Shanghai) Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stearoyl-CoA Desaturase / Triterpenes / Apoptosis / Gallbladder Neoplasms Limits: Animals / Humans Language: En Journal: Acta Biochim Biophys Sin (Shanghai) Year: 2020 Document type: Article