Cryptobrachytone C from Cryptocarya pulchrinervia (Kosterm) Leaves on Proliferation, Apoptosis, Migration and Clonogenicity of MCF-7 and T47D Cell Lines.

IF 17.7 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Accounts of Chemical Research Pub Date : 2023-06-01 Epub Date: 2023-07-21 DOI:10.21315/tlsr2023.34.2.11
Jujun Ratnasari, Marselina Irasonia Tan, Rizkita Rachmi Esyanti, Lia Dewi Juliawaty
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Abstract

Cryptocarya pulchrinervia is an Indonesian indigenous plant that grows in Sumatra, Kalimantan and Papua. One of the new compounds extracted from this plant was cryptobrachytone C, which was known to be cytotoxic against cancer cells of Murine leukemia P388 with IC50 10.52 μM. In this study, the cytotoxicity and anticancer properties of cryptobrachytone C on proliferation, apoptosis, migration and clone formation of MCF-7 and T47D breast cancer cell lines were examined, which had not previously been done before. The cytotoxicity of the compound was measured using an MTT (3- (4,5-dimethylthiazol-2- yl) -2,5-di-phenyl-tetrazolium bromide) assay. The cell proliferation was measured using a BrdU assay, and the cell apoptosis was measured using annexin-V FITC, while the cell migration was measured using a transwell filter. The cytotoxic test result demonstrated that cryptobrachytone C was cytotoxic against MCF-7 cells with IC50 12.94 ± 0.32 μM but not against T47D cells with IC50 65.33 ± 2.33 μM nor against normal MRC-5 cells with IC50 122.57 ± 19.84 μM. The cell proliferation assay showed that cryptobrachytone C at IC50 concentration had antiproliferative properties against MCF-7 cancer cell lines (p < 0.05) but did not significantly reduce T47D cell proliferation (p < 0.07). Although the results of the cell apoptosis test showed that cryptobrachytone C could induce the apoptosis of the MCF-7 and T47D cells, it was insignificant (p > 0.05). The cell migration test showed that cryptobrachytone at IC50 concentrations could inhibit the migration of the MCF-7 and T47D cells. The clonogenic test showed that cryptobrachytone C at IC50 concentration can induce the inhibition of the formation of MCF-7 and T47D cell colonies. The cryptobrachytone C anti-cancer character was more signi icant on the MCF-7 cell line compared to the T47D. This study showed that cryptobrachytone C was cytotoxic and had potential as an anti-cancer compound against MCF-7 and T47D breast cancer cell lines.

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隐卡叶隐短细胞酮C对MCF-7和T47D细胞增殖、凋亡、迁移和克隆原性的影响
粉叶隐车是一种印尼本土植物,生长在苏门答腊、加里曼丹和巴布亚。从该植物中提取的新化合物之一是隐短细胞酮C,已知其对小鼠白血病P388的癌症细胞具有细胞毒性,IC50 10.52?M.本研究检测了隐短细胞酮C对MCF-7和T47D乳腺癌症细胞系增殖、凋亡、迁移和克隆形成的细胞毒性和抗癌特性,这是以前从未做过的。使用MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基-四唑鎓溴化物)测定法测定该化合物的细胞毒性。使用BrdU测定法测量细胞增殖,使用膜联蛋白-V FITC测量细胞凋亡,同时使用transwell过滤器测量细胞迁移。细胞毒性试验结果表明,隐短细胞毒素C对MCF-7细胞具有细胞毒性,IC50为12.94±0.32?M对T47D细胞的IC50为65.33±2.33?M对正常MRC-5细胞的IC50为122.57±19.84?M.细胞增殖试验结果显示,IC50浓度的隐短细胞酮C对MCF-7癌症细胞株具有抗增殖作用(p<0.05),但对T47D细胞增殖无明显抑制作用(p>0.07),细胞迁移实验表明,IC50浓度的隐短细胞酮能抑制MCF-7和T47D细胞的迁移。克隆形成试验表明,IC50浓度的隐短细胞酮C可诱导MCF-7和T47D细胞集落的形成受到抑制。与T47D相比,隐短细胞酮C的抗癌特性在MCF-7细胞系上更显著。本研究表明隐短细胞酮C具有细胞毒性,具有抗MCF-7和T47D乳腺癌症细胞系的抗癌潜力。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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