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姜黄素-塞来昔布:一种用于乳腺癌的协同且合理的联合化疗方案。

Curcumin-Celecoxib: a synergistic and rationale combination chemotherapy for breast cancer.

作者信息

Alqahtani A M, Chidambaram K, Pino-Figueroa A, Chandrasekaran B, Dhanaraj P, Venkatesan K

机构信息

Department of Pharmacology, College of Pharmacy, King Khalid University, Abha, Saudi Arabia.

出版信息

Eur Rev Med Pharmacol Sci. 2021 Feb;25(4):1916-1927. doi: 10.26355/eurrev_202102_25086.

Abstract

OBJECTIVE

Over-expression of COX-2 has been linked with various molecular signaling such as carcinogenesis, invasiveness, and malignant tumour metastasis. Besides, the use of celecoxib is also related to lowering the risk of breast cancer. This study therefore designed to explore the synergistic inhibitory effect of the combination of curcumin and celecoxib on the growth of human breast cancer cells.

MATERIALS AND METHODS

In our investigation, we treated MDA-MB-231 cancer cells with different concentrations of curcumin and celecoxib. The enzyme-linked immunoassay was used to measure the COX-2 expression levels. MDA-MB-231 growth was examined by MTS cell viability assay, and synergy detection was carried out using combination index approaches. The drug-likeliness of the tested drugs (curcumin and celecoxib) were computed and predicted ADME pharmacokinetic parameters by in silico. Further, we have conducted BOILED-Egg plot and bioavailability radar analysis for the curcumin and celecoxib.

RESULTS

The result of the physicochemical and ADMET/pharmacokinetic properties showed that these two drugs have good oral and optically bioavailable absorption. The present in silico study could offer a reliable theoretical basis for future structural modification of these compounds to treat breast cancer. The in vitro results suggested that curcumin and celecoxib individually inhibited the growth of MDA-MB-231 cells in a dose-dependent manner. The effect was synergistic for MDA-MB-231 cells relative to the two compounds individually. The synergistic growth inhibitory effect was mediated by a mechanism that possibly involves inhibition of the COX-2 pathways.

CONCLUSIONS

Our findings show the prominent anti-proliferative effects of celecoxib and/or curcumin on MDA-MB-231 cells, providing a rationale for further detailed preclinical and potential clinical studies of this combination for breast cancer therapy. Further, these computed parameters suggested that curcumin possesses a high tendency to act as an adjuvant drug with celecoxib in the treatment of breast cancer.

摘要

目的

环氧合酶-2(COX-2)的过表达与多种分子信号传导相关,如致癌作用、侵袭性和恶性肿瘤转移。此外,塞来昔布的使用也与降低乳腺癌风险有关。因此,本研究旨在探讨姜黄素与塞来昔布联合应用对人乳腺癌细胞生长的协同抑制作用。

材料与方法

在我们的研究中,我们用不同浓度的姜黄素和塞来昔布处理MDA-MB-231癌细胞。采用酶联免疫吸附测定法测量COX-2表达水平。通过MTS细胞活力测定法检测MDA-MB-231细胞的生长情况,并使用联合指数方法进行协同作用检测。计算受试药物(姜黄素和塞来昔布)的类药性质,并通过计算机模拟预测其ADME药代动力学参数。此外,我们还对姜黄素和塞来昔布进行了水煮蛋图和生物利用度雷达分析。

结果

理化性质和ADMET/药代动力学性质的结果表明,这两种药物具有良好的口服和光学生物可利用吸收性。目前的计算机模拟研究可为这些化合物未来用于治疗乳腺癌的结构修饰提供可靠的理论依据。体外实验结果表明,姜黄素和塞来昔布均可剂量依赖性地抑制MDA-MB-231细胞的生长。相对于单独使用这两种化合物,对MDA-MB-231细胞的作用具有协同性。协同生长抑制作用可能是通过抑制COX-2途径介导的。

结论

我们的研究结果表明塞来昔布和/或姜黄素对MDA-MB-231细胞具有显著的抗增殖作用,为该联合用药用于乳腺癌治疗的进一步详细临床前和潜在临床研究提供了理论依据。此外,这些计算参数表明姜黄素在乳腺癌治疗中具有作为塞来昔布辅助药物的高度倾向。

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