Anticancer Activity of Tetrandrine by Inducing Apoptosis in Human Breast Cancer Cell Line MDA-MB-231 In Vivo.
Chun-Hui WangJia-Min YangYu-Bo GuoJing ShenXiao-Hua PeiPublished in: Evidence-based complementary and alternative medicine : eCAM (2020)
Tetrandrine (TET) is an alkaloid extracted from a traditional Chinese medicinal plant. It exerts remarkable anticancer activity and induces apoptotic cell death in various human cancer cells. The present study aimed to investigate the effects of TET on the inhibition of tumor growth and the induction of apoptosis in MDA-MB-231 breast cancer in xenograft mice. Tumor weight and volume were measured. The histopathological changes in the tumor tissue were observed. Immunohistochemistry analysis of Bcl-2-associated X protein (Bax) and B-cell lymphoma/leukemia-2 (Bcl-2) was carried out. The expression of apoptosis-associated genes and proteins, such as cysteine aspartic acid-specific protease-3 (Caspase-3), Survivin, Bax, Bcl-2, BH3-interacting domain death agonist (Bid), and poly ADP-ribose polymerase (PARP), was measured by reverse transcription-polymerase chain reaction (RT-PCR) and Western blotting, respectively. TET inhibited tumor growth and induced apoptosis in TNBC cell line MDA-MB-231. The mechanism underlying this effect might be mediated by TET-upregulated Caspase-3, Bax, and Bid and downregulated by Bcl-2, Survivin, and PARP. Taken together, this study supported the fact that TET is a promising therapeutic agent for the treatment of TNBC, thereby providing experimental evidence for its use in the treatment of breast cancer.
Keyphrases
- induced apoptosis
- cell death
- cell cycle arrest
- endoplasmic reticulum stress
- oxidative stress
- signaling pathway
- endothelial cells
- dna damage
- pi k akt
- breast cancer cells
- dna repair
- body mass index
- bone marrow
- poor prognosis
- type diabetes
- transcription factor
- south africa
- physical activity
- gene expression
- diffuse large b cell lymphoma
- insulin resistance
- protein protein
- weight gain
- combination therapy
- induced pluripotent stem cells
- drug discovery
- genome wide
- breast cancer risk