Natural Terpenoids Against Female Breast Cancer: A 5-year Recent Research

被引:58
|
作者
Ateba, Sylvin Benjamin [1 ]
Mvondo, Marie Alfrede [2 ]
Ngeu, Sadrine Tchoukouegno [3 ]
Tchoumtchoual', Job [1 ,4 ]
Awounfackl, Charline Florence [1 ]
Njamen, Dieudonne [1 ]
Krenn, Liselotte [5 ]
机构
[1] Univ Yaounde I, Fac Sci, Dept Anim Biol & Physiol, Lab Anim Physiol, POB 812, Yaounde, Cameroon
[2] Univ Dschang, Fac Sci, Dept Anim Biol, Lab Anim Physiol & Phytopharmacol, POB 67, Dschang, Cameroon
[3] Protestant Univ Cent Africa, Fac Hlth Sci, POB 4011, Yaounde, Cameroon
[4] Univ Athens, Fac Pharm, Div Pharmacognosy & Nat Prod Chem, GR-15771 Athens, Greece
[5] Univ Vienna, Dept Pharmacognosy, Althanstr 14, A-1090 Vienna, Austria
关键词
Breast; anti-cancer; terpenoids/terpenes; carcinogenesis; breast cancer; breast cancer treatment; CELL-CYCLE ARREST; EPITHELIAL-MESENCHYMAL TRANSITION; PEGYLATED NANOLIPOSOMAL ARTEMISININ; CYTOTOXIC SESQUITERPENE LACTONES; GROWTH-INHIBITORY ACTIVITY; MTT-BASED ASSAY; IN-VITRO; DOWN-REGULATION; CUCURBITACIN B; TUMOR ANGIOGENESIS;
D O I
10.2174/0929867325666180214110932
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
Background: The approval of Taxol (R) in 1993 marked the great entrance of terpenoids in the anti-cancer area and this drug is still highly important in the treatment of refractory ovarian, breast and other cancers. Over decades, other prominent natural terpenoids have become indispensable for the modern pharmacotherapy of breast cancer. However, given the rapid evolution of drug resistance, effective treatments for advanced breast cancers requiring cytotoxic chemotherapy represent a major unmet clinical need. Therefore, innovative agents effective in long-term chemotherapy are urgently needed. Objective: This review examines recent advances/research about natural terpenoids, and their mechanisms against female breast cancer over the period covering January 1st, 2012 to December 31st, 2016. Results: Carcinogenesis constitutes a multistep process wherein each stage is characterized by distinct phenotypic changes. Numerous chemicals recorded in this review have been shown to significantly inhibit proliferation, migration, apoptosis resistance, tumor angiogenesis or metastasis in different breast cancer cells/tumours in vitro and in vivo. Targeting simultaneously several or all these aspects/steps of cancer progression could be an advantage. In line with this, phytochemicals such as thymoquinone (8), costunolide (46), tanshinone IIA (132), triptolide (136), cucurbitacin B (179), celastrol (226) and lycopene (238) had caught our attention. Conclusion: These compounds appear to be promising to overcome breast cancer treatment failure. However, despite the interesting activities, additional preclinical investigations are needed in further breast cancer cell/tumor models in vitro and in vivo.
引用
收藏
页码:3162 / 3213
页数:52
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