Marine anticancer drugs in modulating miRNAs and antioxidant signaling

被引:1
|
作者
Chuang, Ya-Ting [1 ]
Yen, Ching-Yu [2 ,3 ]
Tang, Jen-Yang [4 ,5 ]
Wu, Kuo-Chuan [6 ]
Chang, Fang-Rong [7 ]
Tsai, Yi-Hong [8 ]
Chien, Tsu-Ming [4 ,9 ,10 ]
Chang, Hsueh-Wei [1 ,11 ,12 ]
机构
[1] Kaohsiung Med Univ, Coll Life Sci, Dept Biomed Sci & Environm Biol, PhD Program Life Sci, Kaohsiung 80708, Taiwan
[2] Taipei Med Univ, Sch Dent, Taipei 11031, Taiwan
[3] Chi Mei Med Ctr, Dept Oral & Maxillofacial Surg, Tainan 71004, Taiwan
[4] Kaohsiung Med Univ, Sch Postbaccalaureate Med, Kaohsiung 80708, Taiwan
[5] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Dept Radiat Oncol, Kaohsiung 80708, Taiwan
[6] Natl Pingtung Univ, Dept Comp Sci & Informat Engn, Pingtung 900392, Taiwan
[7] Kaohsiung Med Univ, Grad Inst Nat Prod, Kaohsiung 80708, Taiwan
[8] Tajen Univ, Coll Pharm & Hlth Care, Dept Pharm & Master Program, Pingtung 907101, Taiwan
[9] Kaohsiung Med Univ Hosp, Dept Urol, Kaohsiung 80708, Taiwan
[10] Kaohsiung Med Univ, Kaohsiung Gangshan Hosp, Dept Urol, Kaohsiung 820111, Taiwan
[11] Kaohsiung Med Univ, Ctr Canc Res, Kaohsiung 80708, Taiwan
[12] Kaohsiung Med Univ Hosp, Dept Med Res, Kaohsiung 80708, Taiwan
关键词
Marine natural products; Anticancer; miRNAs; Antioxidant signaling; BREAST-CANCER CELLS; HEPATOCELLULAR-CARCINOMA; OXIDATIVE STRESS; MITOCHONDRIAL DYSFUNCTION; INHIBITS PROLIFERATION; DEPENDENT APOPTOSIS; EXPRESSION; PROTECTS; AXIS; PROGRESSION;
D O I
10.1016/j.cbi.2024.111142
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several marine drugs exert anticancer effects by inducing oxidative stress, which becomes overloaded and kills cancer cells when redox homeostasis is imbalanced. The downregulation of antioxidant signaling induces oxidative stress, while its upregulation attenuates oxidative stress. Marine drugs have miRNA-modulating effects against cancer cells. However, the potential antioxidant targets of such drugs have been rarely explored. This review aims to categorize the marine-drug-modulated miRNAs that downregulate their antioxidant targets, causing oxidative stress in anticancer treatments. We also categorize the downregulation of oxidative-stress- inducing miRNAs in antioxidant protection among non-cancer cells. We summarize the putative antioxidant targets of miRNA-modulating marine drugs by introducing a bioinformatics tool (miRDB). Finally, the marine drugs affecting antioxidant targets are surveyed. In this way, the connections between marine drugs and their modulating miRNA and antioxidant targets are innovatively categorized to provide a precise network for exploring their potential anticancer functions and protective effects on non-cancer cells.
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收藏
页数:14
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