Development of Ethanolic Extract of Pinang Masak Jambi (Areca Catechu L.) as A Modulator of Doxorubicin Cytotoxic Effect in Breast Cancer Therapy

F. Fitrianingsih, Indri Maharini, Diah Tri Utami
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Abstract

Doxorubicin is one of the chemotherapy agents that is often used in breast cancer therapy. Phenomenon of breast cancer cell resistance to chemotherapy agents has been traced to the molecular level. The development of compounds that can overcome drug resistance chemotherapy needs to be continuously developed, especially agents with specific molecular targets, namely P-glycoprotein (Pgp), NFkB, cyclin, and cyclin-dependent kinase (CDK). Another alternative is the combination of chemotherapy agents with chemopreventive agents (co-chemotherapy) to reduce side effects and increase sensitivity of cancer cells. Doxorubicin is often used in breast cancer therapy. This study was performed to determine the effect of ethanolic extract of Pinang Masak Jambi ( Areca catechu L.) (EEPMJ) and doxorubicin combination on MCF-7 breast cancer cells. Cytotoxic assay of EEPMJ and doxorubicin, alone, or in combination, was done using MTT test method to determine the IC 50 and CI (Combination Index) values. The results indicated that EEPMJ and doxorubicin had IC 50 values of 75.1 µg/ml and 22 µg/ml, respectively. Based on CI values, all combination concentration showed varying CI values. The concentration of 1/8 IC 50 of EEPMJ with 1/2, 1/4, and 1/8 IC50 of doxorubicin showed a strong synergistic effect (CI 0.1 - 0.3), with the inhibition of cell viability up to 67.39%. This synergistic effect occurs because EEPMJ potentially could increases the cytotoxicity of doxorubicin.
槟榔槟榔醇提物在乳腺癌治疗中阿霉素细胞毒作用的研究
阿霉素是一种常用于乳腺癌治疗的化疗药物。乳腺癌细胞对化疗药物的耐药现象已经追溯到分子水平。克服耐药化疗的化合物需要不断开发,特别是具有特定分子靶点的药物,即p -糖蛋白(Pgp)、NFkB、细胞周期蛋白和细胞周期蛋白依赖性激酶(CDK)。另一种选择是化疗药物与化学预防药物的联合化疗(联合化疗),以减少副作用并增加癌细胞的敏感性。阿霉素常用于乳腺癌治疗。本研究旨在探讨槟榔槟榔醇提物(EEPMJ)与阿霉素联合使用对MCF-7乳腺癌细胞的影响。采用MTT法测定EEPMJ与阿霉素单独或联合使用的细胞毒性,测定ic50和CI(联合指数)值。结果表明,EEPMJ和阿霉素的ic50值分别为75.1µg/ml和22µg/ml。从CI值来看,所有组合浓度的CI值都不同。EEPMJ与阿霉素的1/2、1/4、1/8 IC50浓度均表现出较强的协同效应(CI 0.1 ~ 0.3),对细胞活力的抑制率达67.39%。这种协同效应的发生是因为EEPMJ可能会增加阿霉素的细胞毒性。
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