Secalonic acid D induces cell apoptosis in both sensitive and ABCG2-overexpressing multidrug resistant cancer cells through upregulating c-Jun expression
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  • 英文篇名:Secalonic acid D induces cell apoptosis in both sensitive and ABCG2-overexpressing multidrug resistant cancer cells through upregulating c-Jun expression
  • 作者:Hong ; Zhang ; Liyan ; Huang ; Liyang ; Tao ; Jianye ; Zhang ; Fang ; Wang ; Xu ; Zhang ; Liwu ; Fu
  • 英文作者:Hong Zhang;Liyan Huang;Liyang Tao;Jianye Zhang;Fang Wang;Xu Zhang;Liwu Fu;Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangdong Esophageal Cancer Institute;School of Pharmaceutical Sciences, Guangzhou Medical University;
  • 英文关键词:Multidrug resistance;;Secalonic acid D;;Apoptosis;;c-Jun;;ABCG2
  • 中文刊名:YXBY
  • 英文刊名:药学学报(英文)
  • 机构:Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangdong Esophageal Cancer Institute;School of Pharmaceutical Sciences, Guangzhou Medical University;
  • 出版日期:2019-05-25
  • 出版单位:Acta Pharmaceutica Sinica B
  • 年:2019
  • 期:v.9
  • 基金:supported by grants from the National Science & Technology Major Project “Key New Drug Creation and Manufacturing Program” (No. 2018ZX09711002, China);; Science and Technology Foundation of Guangdong Province (No. 2016A030312014, China);; Guangzhou Science and Technology Program (No. 201707010048, China);; from the Scientific and Technological Leading Talent Project of Guangdong Province (2015, China)
  • 语种:英文;
  • 页:YXBY201903007
  • 页数:10
  • CN:03
  • ISSN:10-1171/R
  • 分类号:72-81
摘要
Secalonic acid D(SAD) could inhibit cell growth in not only sensitive cells but also multidrug resistant(MDR) cells. However, the molecular mechanisms need to be elucidated. Here, we identified that SAD possessed potent cytotoxicity in 3 pairs of MDR and their parental sensitive cells including S1-MI-80 and S1,H460/MX20 and H460, MCF-7/ADR and MCF-7 cells. Furthermore, SAD induced cell G2/M phase arrest via the downregulation of cyclin B1 and the increase of CDC2 phosphorylation. Importantly, JNK pathway upregulated the expression of c-Jun in protein level and increased c-Jun phosphorylation induced by SAD, which was linked to cell apoptosis via c-Jun/Src/STAT3 pathway. To investigate the mechanisms of upregulation of c-Jun protein by SAD, the mR NA expression level and degradation of c-Jun were examined. We found that SAD did not alter the mR NA level of c-Jun but inhibited its proteasome-dependent degradation. Taken together, these results implicate that SAD induces cancer cell death through c-Jun/Src/STAT3 signaling axis by inhibiting the proteasome-dependent degradation of c-Jun in both sensitive cells and ATP-binding cassette transporter sub-family G member 2(ABCG2)-mediated MDR cells.
        Secalonic acid D(SAD) could inhibit cell growth in not only sensitive cells but also multidrug resistant(MDR) cells. However, the molecular mechanisms need to be elucidated. Here, we identified that SAD possessed potent cytotoxicity in 3 pairs of MDR and their parental sensitive cells including S1-MI-80 and S1,H460/MX20 and H460, MCF-7/ADR and MCF-7 cells. Furthermore, SAD induced cell G2/M phase arrest via the downregulation of cyclin B1 and the increase of CDC2 phosphorylation. Importantly, JNK pathway upregulated the expression of c-Jun in protein level and increased c-Jun phosphorylation induced by SAD, which was linked to cell apoptosis via c-Jun/Src/STAT3 pathway. To investigate the mechanisms of upregulation of c-Jun protein by SAD, the mR NA expression level and degradation of c-Jun were examined. We found that SAD did not alter the mR NA level of c-Jun but inhibited its proteasome-dependent degradation. Taken together, these results implicate that SAD induces cancer cell death through c-Jun/Src/STAT3 signaling axis by inhibiting the proteasome-dependent degradation of c-Jun in both sensitive cells and ATP-binding cassette transporter sub-family G member 2(ABCG2)-mediated MDR cells.
引文
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