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Evaluation of heterocyclic steroids and curcumin derivatives as anti breast cancer agents: Studying the effect on apoptosis in MCF-7 breast cancer cells
被引:36
|作者:
Elmegeed, Gamal A.
[1
]
Yahya, Shaymaa M. M.
[1
]
Abd-Elhalim, Mervat M.
[1
]
Mohamed, Mervat S.
[2
,3
]
Mohareb, Rafat M.
[2
]
Elsayed, Ghada H.
[1
]
机构:
[1] Natl Res Ctr, Hormones Dept, Giza 12622, Egypt
[2] Cairo Univ, Dept Chem, Fac Sci, Cairo, Egypt
[3] Cairo Univ, Biochem Special, Fac Sci, Cairo, Egypt
来源:
关键词:
Apoptotic genes;
Breast cancer;
Cytotoxicity;
Heterocycles;
Steroids;
GROWTH-INHIBITION;
CYCLIN D1;
SURVIVIN;
DEATH;
P53;
MEDIATOR;
D O I:
10.1016/j.steroids.2016.08.014
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:
Anticancer agents consisting of hybrid molecules are used to improve effectiveness and diminish drug resistance. The current study aimed to introduce newly synthesized hetero-steroids of promising anticancer effects. Besides, the pro-apoptotic effects of new compounds were investigated extensively. Several pyrimidino-, triazolopyrimidino-, pyridazino-, and curcumin-steroid derivatives were synthesized, elucidated and confirmed using the spectral and analytical data. The synthesized hetero-steroids, compounds 9, 10, 11, 12, 13, 14, 15, 18, 20, 21, 22 and 24, were tested for their cytotoxic effects versus human breast cancer cells (MCF-7) using neutral red supravital dye uptake assay. Compound 24 (IC50 = 18 mu M) showed more inhibitory influence on MCF-7 growth. Using QRT-PCR (Quantitative real time-polymerase chain reaction), CCND1, Survivin, BCL-2, CDC2, P21 and P53, genes expression levels were investigated. The study results disclose that compounds 4, 7, 18, 24 knocked down the expression levels of CCND1, Survivin, BCL-2 and CDC2. However, P21 and P53 were up-regulated by compounds 21, 22. This study introduced promising pro-apoptotic anticancer agents acting through the modulation of key regulators of apoptosis and cell cycle genes. (C) 2016 Elsevier Inc. All rights reserved.
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页码:80 / 89
页数:10
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