Betulinic acid: A natural promising anticancer drug, current situation, and future perspectives

被引:23
|
作者
Aswathy, Maniyamma [1 ,2 ]
Vijayan, Ajesh [3 ]
Daimary, Uzini D. [4 ]
Girisa, Sosmitha [4 ]
Radhakrishnan, Kokkuvayil, V [1 ]
Kunnumakkara, Ajaikumar B. [4 ]
机构
[1] Natl Inst Interdisciplinary Sci & Technol CSIR NI, Chem Sci & Technol Div, Thiruvananthapuram 695019, Kerala, India
[2] Acad Sci & Innovat Res AcSIR, Ghaziabad, India
[3] CHRIST Deemed Univ, Dept Chem, Bangalore, Karnataka, India
[4] Indian Inst Technol, Dept Biosci & Bioengn, Canc Biol Lab, Room 005,O Block, Gauhati 781039, Assam, India
关键词
anticancer; apoptosis; betulin; betulinic acid; cytotoxicity; hydrosolubility; pharmacokinetics; ENDOTHELIAL GROWTH-FACTOR; SQUAMOUS-CELL CARCINOMA; TRIPLE NEGATIVE BREAST; PROSTATE-CANCER CELLS; KAPPA-B ACTIVATION; IN-VITRO; MEDIATED APOPTOSIS; STAT3; ACTIVATION; ALPHA; CURCUMIN;
D O I
10.1002/jbt.23206
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
Natural products serve as the single most productive source for the discovery of drugs and pharmaceutical leads. Among the various chemicals derived from microbes, plants, and animals, phytochemicals have emerged as potential candidates for the development of anticancer drugs due to their structural diversities, complexities, and pleiotropic effects. Herein, we discuss betulinic acid (BA), a ubiquitously distributed lupane structured pentacyclic triterpenoid, scrutinized as a promising natural agent for the prevention, suppression, and management of various human malignancies. Ease of availability, common occurrences, cell-specific cytotoxicity, and astonishing selectivity are the important factors that contribute to the development of BA as an anticancer agent. The current review delineates the mechanistic framework of BA-mediated cancer suppression through the modulation of multiple signaling pathways and also summarizes the key outcomes of BA in preclinical investigations.
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页数:18
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