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基于基质金属蛋白酶 9 的导向分离及其对乳腺癌细胞模型的细胞毒性: 计算机模拟和体外研究(第二部分)。

Bioguided Fractionation of Local Plants against Matrix Metalloproteinase9 and Its Cytotoxicity against Breast Cancer Cell Models: In Silico and In Vitro Study (Part II).

机构信息

Drug Discovery Student Club, Faculty of Pharmacy, Campus III, Sanata Dharma University, Paingan, Maguwoharjo, Depok, Sleman, Yogyakarta 55282, Indonesia.

Bachelor in Pharmacy Program, Faculty of Science and Technology, Ma Chung University, Malang 65151, Indonesia.

出版信息

Molecules. 2021 Mar 8;26(5):1464. doi: 10.3390/molecules26051464.

DOI:10.3390/molecules26051464
PMID:33800366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7962846/
Abstract

In our previous work, the partitions (1 mg/mL) of (AC) aerial parts and (IC) leaves showed inhibitions of 94% and 96%, respectively, whereas their fractions showed IC 43 and 116 µg/mL, respectively, toward Matrix Metalloproteinase9 (MMP9), an enzyme that catalyzes a proteolysis of extracellular matrix. In this present study, we performed IC determinations for AC -hexane, IC -hexane, and IC ethylacetate partitions, followed by the cytotoxicity study of individual partitions against MDA-MB-231, 4T1, T47D, MCF7, and Vero cell lines. Successive fractionations from AC -hexane and IC ethylacetate partitions led to the isolation of two compounds, oxytetracycline (OTC) and dioctyl phthalate (DOP). The result showed that AC -hexane, IC -hexane, and IC ethylacetate partitions inhibit MMP9 with their respective IC as follows: 246.1 µg/mL, 5.66 µg/mL, and 2.75 × 10 µg/mL. Toward MDA-MB-231, 4T1, T47D, and MCF7, AC -hexane demonstrated IC 2.05, 265, 109.70, and 2.11 µg/mL, respectively, whereas IC ethylacetate showed IC 1.92, 57.5, 371.5, and 2.01 µg/mL, respectively. The inhibitions toward MMP9 by OTC were indicated by its IC 18.69 µM, whereas DOP was inactive. A molecular docking study suggested that OTC prefers to bind to PEX9 rather than its catalytic domain. Against 4T1, OTC showed inhibition with IC 414.20 µM. In conclusion, this study furtherly supports the previous finding that AC and IC are two herbals with potential to be developed as triple-negative anti-breast cancer agents.

摘要

在我们之前的工作中,(AC)地上部分和(IC)叶子的部分(1mg/mL)分别显示出 94%和 96%的抑制作用,而它们的馏分则分别显示出基质金属蛋白酶 9(MMP9)的 IC 43 和 116μg/mL,MMP9 是一种催化细胞外基质蛋白水解的酶。在本研究中,我们对 AC-己烷、IC-己烷和 IC 乙酸乙酯部分进行了 IC 测定,然后对各部分进行了细胞毒性研究,以 MDA-MB-231、4T1、T47D、MCF7 和 Vero 细胞系。从 AC-己烷和 IC 乙酸乙酯部分的连续分馏导致了两种化合物的分离,即土霉素(OTC)和邻苯二甲酸二辛酯(DOP)。结果表明,AC-己烷、IC-己烷和 IC 乙酸乙酯部分抑制 MMP9 的 IC 分别为:246.1μg/mL、5.66μg/mL 和 2.75×10μg/mL。对 MDA-MB-231、4T1、T47D 和 MCF7,AC-己烷表现出 IC 2.05、265、109.70 和 2.11μg/mL,而 IC 乙酸乙酯表现出 IC 1.92、57.5、371.5 和 2.01μg/mL。OTC 的 MMP9 抑制作用表明其 IC 为 18.69μM,而 DOP 无活性。分子对接研究表明,OTC 更喜欢与 PEX9 结合而不是其催化结构域。对 4T1,OTC 显示出 IC 414.20μM 的抑制作用。综上所述,本研究进一步支持了之前的发现,即 AC 和 IC 是两种具有开发潜力的三阴性抗乳腺癌药物的草药。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/95d190991f0f/molecules-26-01464-g013.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/a3d3cf6515d3/molecules-26-01464-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/9ef4133a269b/molecules-26-01464-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/43ff19f7f135/molecules-26-01464-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/ac214d66e6f2/molecules-26-01464-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/4e07a9397a3b/molecules-26-01464-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/c957ae9efaa9/molecules-26-01464-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/43754b10d8da/molecules-26-01464-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/b3377b52e016/molecules-26-01464-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/95d190991f0f/molecules-26-01464-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/cb6265e521fc/molecules-26-01464-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/ca0c85505a56/molecules-26-01464-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/0a274c45543c/molecules-26-01464-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/8c073216d3c9/molecules-26-01464-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/a3d3cf6515d3/molecules-26-01464-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/9ef4133a269b/molecules-26-01464-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/43ff19f7f135/molecules-26-01464-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/ac214d66e6f2/molecules-26-01464-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/4e07a9397a3b/molecules-26-01464-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/c957ae9efaa9/molecules-26-01464-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/43754b10d8da/molecules-26-01464-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/b3377b52e016/molecules-26-01464-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a71c/7962846/95d190991f0f/molecules-26-01464-g013.jpg

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