Mousavi-Koodehi Batool, Darzi Leila, Sadeghizadeh Majid, Najafi Farhood, Forouzandeh-Moghdam Mehdi
Department of Medical Biotechnology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.
Department of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.
Life Sci. 2022 Mar 15;293:120308. doi: 10.1016/j.lfs.2022.120308. Epub 2022 Jan 10.
Metformin hydrochloride is a highly hydrophilic molecule with low permeability. In the present study, to develop an effective drug to treat the metastatic breast cancer, metformin caprylic acid was synthesized using metformin hydrochloride as a permeable agent.
The cytotoxic effects of various concentrations of metformin caprylic acid and metformin hydrochloride (0 to 20 mM) on MCF-7 and MDA-MB-231 breast cancer cells and MCF-10A human mammary epithelial cell line were assessed by the MTT assay. Furthermore, Annexin V, PI staining, and cell flow cytometry assays were performed to evaluate the apoptotic effects. The invasion and migration ability of these cells were evaluated following treatment with equal concentration (3 mM) of the two compounds.
The treatment of tested cell lines with an equal concentration of two chemicals decreased cell viability in a time and dose-dependent manner, where in all cases, metformin caprylic acid caused significantly more apoptosis and invasion inhibition than that of metformin hydrochloride (*p < 0.05). Chemical structures of both compounds were confirmed by FTIR and H NMR, C NMR. Both chemicals inhibited the migration of MCF-7 and MCF-10A cells, but had no effect on MDA-MB-231 migration. All data are expressed as mean ± SD (n = 3).
It seems that in an equal concentration, the similarity of the hydrophobic tail of caprylic acid to the cell membrane improves its entrance, while decreasing the drug excretion.
盐酸二甲双胍是一种亲水性高、渗透性低的分子。在本研究中,为开发一种治疗转移性乳腺癌的有效药物,以盐酸二甲双胍为渗透剂合成了辛酸二甲双胍。
采用MTT法评估不同浓度的辛酸二甲双胍和盐酸二甲双胍(0至20 mM)对MCF-7和MDA-MB-231乳腺癌细胞以及MCF-10A人乳腺上皮细胞系的细胞毒性作用。此外,进行了膜联蛋白V、碘化丙啶染色和细胞流式细胞术检测以评估凋亡作用。用两种化合物的等浓度(3 mM)处理后评估这些细胞的侵袭和迁移能力。
用两种化学物质的等浓度处理受试细胞系,细胞活力呈时间和剂量依赖性降低,在所有情况下,辛酸二甲双胍引起的凋亡和侵袭抑制均明显多于盐酸二甲双胍(*p < 0.05)。两种化合物的化学结构通过傅里叶变换红外光谱(FTIR)、氢核磁共振(H NMR)和碳核磁共振(C NMR)得以确认。两种化学物质均抑制MCF-7和MCF-10A细胞的迁移,但对MDA-MB-231细胞的迁移无影响。所有数据均表示为平均值±标准差(n = 3)。
似乎在等浓度下,辛酸的疏水尾部与细胞膜的相似性提高了其进入细胞的能力,同时减少了药物排泄。