Betulinic acid and oleanolic acid modulate CD81 expression and induce apoptosis in triple-negative breast cancer cells through ROS generation
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作者:
Lestari, Dian Yuliartha
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Univ Airlangga, Fac Med, Doctoral Program Med Sci, Surabaya, Indonesia
Univ Muhammadiyah Malang, Med Fac, Malang, IndonesiaUniv Airlangga, Fac Med, Doctoral Program Med Sci, Surabaya, Indonesia
Lestari, Dian Yuliartha
[1
,2
]
Mastutik, Gondo
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Univ Airlangga, Fac Med, Dept Pathol Anat, Surabaya, IndonesiaUniv Airlangga, Fac Med, Doctoral Program Med Sci, Surabaya, Indonesia
Mastutik, Gondo
[3
]
Mukono, Indri Safitri
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Univ Airlangga, Fac Med, Dept Physiol & Med Biochem, Surabaya, IndonesiaUniv Airlangga, Fac Med, Doctoral Program Med Sci, Surabaya, Indonesia
Mukono, Indri Safitri
[4
]
机构:
[1] Univ Airlangga, Fac Med, Doctoral Program Med Sci, Surabaya, Indonesia
[2] Univ Muhammadiyah Malang, Med Fac, Malang, Indonesia
[3] Univ Airlangga, Fac Med, Dept Pathol Anat, Surabaya, Indonesia
[4] Univ Airlangga, Fac Med, Dept Physiol & Med Biochem, Surabaya, Indonesia
Triple-negative breast cancer (TNBC) is an aggressive subtype of breast cancer characterized by a lack of hormones receptors and the HER2 receptor, making it unresponsive to targeted therapy. Triterpenoids such as betulinic acid (BA) and oleanolic acid (OA) have anticancer effects by inducing apoptosis in TNBC cells. CD81 is a tetraspanin that affects the growth and metastasis of cancer cells. To examine the effect of BA and OA on the viability of TNBC cell line (MDA-MB 231) by analyzing the CD81 expression, intracellular ROS, and apoptosis. The MDA-MB 231 cells was cultured and treated by BA and OA. The viability cell was evaluated by the CCK8 assay. This study analyzed the binding of BA and OA with CD81 using molecular docking and evaluated CD81 expression, intracellular ROS, and apoptosis by flow cytometry. The result showed that BA and OA inhibited viability of MDA-MB-231 cells. BA and OA bind to CD81 in silico, with binding affinities of 9.0 kcal/mol for BA and 7.2 kcal/mol for OA. Flow cytometry results revealed that BA can downregulate CD81 expression. BA and OA also increased intracellular ROS levels and induced apoptosis. These findings suggest that BA and OA, especially BA, can modulate CD81 expression and promote apoptosis in TNBC cells through the generation of ROS, thereby offering a potential therapeutic strategy for the treatment of TNBC.
机构:
Tianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R ChinaTianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R China
Li, Dongdong
Wang, Luyao
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Tianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R ChinaTianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R China
Wang, Luyao
Yaguee, Ernesto
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Imperial Coll London, Fac Med, Div Canc, Canc Res Ctr, Hammersmith Hosp Campus, London W12 0NN, EnglandTianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R China
Yaguee, Ernesto
Dai, Linlin
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Tianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R ChinaTianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R China
Dai, Linlin
Zhao, Xiumei
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Tianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R ChinaTianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R China
Zhao, Xiumei
Yang, Zibo
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Tianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R ChinaTianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R China
Yang, Zibo
Zhi, Shuang
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Tianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R ChinaTianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R China
Zhi, Shuang
Hu, Yunhui
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Tianjin Med Univ, Canc Inst & Hosp, Dept Breast Canc 3, Tianjin 300060, Peoples R ChinaTianjin Inst Med & Pharmaceut Sci, Tianjin 300020, Peoples R China
机构:
Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R ChinaGuangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
Xie, Yikun
Su, Yifan
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Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R ChinaGuangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
Su, Yifan
Liao, Zirou
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Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R ChinaGuangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
Liao, Zirou
Liang, Xinran
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Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R ChinaGuangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
Liang, Xinran
Hua, Jing
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机构:
Guangxi Normal Univ, State Key Lab Chem & Mol Engn Med Resources, Guilin 541004, Peoples R ChinaGuangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
Hua, Jing
Zhang, Dawei
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Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R ChinaGuangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
Zhang, Dawei
Hu, Dexuan
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机构:
Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Peoples R ChinaGuangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
Hu, Dexuan
Yu, Qian
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Guangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
Guangxi Normal Univ, State Key Lab Chem & Mol Engn Med Resources, Guilin 541004, Peoples R ChinaGuangdong Pharmaceut Univ, Sch Pharm, Guangzhou 510006, Peoples R China
机构:
China Acad Chinese Med Sci, Wangjing Hosp, Div Gen Surg, Beijing 100102, Peoples R ChinaChina Acad Chinese Med Sci, Wangjing Hosp, Div Gen Surg, Beijing 100102, Peoples R China
Wang, Changcheng
Guo, Jia
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China Acad Chinese Med Sci, Wangjing Hosp, Div Gen Surg, Beijing 100102, Peoples R ChinaChina Acad Chinese Med Sci, Wangjing Hosp, Div Gen Surg, Beijing 100102, Peoples R China
Guo, Jia
Wu, Zeng'An
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China Acad Chinese Med Sci, Wangjing Hosp, Div Gen Surg, Beijing 100102, Peoples R ChinaChina Acad Chinese Med Sci, Wangjing Hosp, Div Gen Surg, Beijing 100102, Peoples R China