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香草酸对子宫内膜癌大鼠氧化还原稳态、基质金属蛋白酶和细胞周期蛋白D1调节的预防作用

Preventive Efficacy of Vanillic Acid on Regulation of Redox Homeostasis, Matrix Metalloproteinases and Cyclin D1 in Rats Bearing Endometrial Carcinoma.

作者信息

Bhavani Pakkiri, Subramanian Perumal, Kanimozhi Sivamani

机构信息

Department of Biochemistry and Biotechnology, Faculty of Science, Annamalai University, Chidambaram, Tamil Nadu 608002 India.

出版信息

Indian J Clin Biochem. 2017 Oct;32(4):429-436. doi: 10.1007/s12291-016-0605-6. Epub 2016 Aug 24.

Abstract

Endometrial carcinoma is a malignant tumor of the female genital tract. This study has been performed to evaluate the chemopreventive efficacy of vanillic acid (a bio flavonoid) on endometrial carcinoma (EC) by assessing the levels of thiobarbituric acid reactive substances (TBARS), lipid hydroperoxides (LOOH), cytochrome P450, antioxidants-superoxide dismutase (SOD), catalase (CAT), glutathione peroxides (GPx), reduced glutathione (GSH), vitamins C and E, matrix metalloproteinases (MMP-2 and 9) and cell cycle check point protein (cyclin D1) in -methyl-'-nitro--nitrosoguanidine (MNNG) induced carcinogenic rats. EC provoked by intravaginal detention of MNNG (150 mg/kg b.w. for 90 days), lead to enhancement of the levels of TBARS, LOOH, cytochrome P450, and decrement in the levels of antioxidants (SOD, CAT, GPx, GSH, vitamins C and E) and upregulated expression of MMP-2 and 9 and cyclin D1 (by western blot analysis). The treatment of vanillic acid (100 mg/kg b.w.) to MNNG treated rats (1) normalized the histopathological alterations, (2) reduced the levels of TBARS, LOOH and cytochrome P450 (3) increased the levels of antioxidants (SOD, CAT, GPx, GSH, vitamins C and E) in plasma and uterus and (4) down regulated the expression of MMP-2, 9 and cyclin D1. The effect of vanillic acid is more predominant in pre-treatment group than co-treated rats. Our results designate that vanillic acid inhibits the EC by elevating antioxidants and by regulating the levels of metalloproteinase and cell cycle check point protein.

摘要

子宫内膜癌是女性生殖道的一种恶性肿瘤。本研究旨在通过评估硫代巴比妥酸反应性物质(TBARS)、脂质氢过氧化物(LOOH)、细胞色素P450、抗氧化剂——超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、谷胱甘肽过氧化物酶(GPx)、还原型谷胱甘肽(GSH)、维生素C和E、基质金属蛋白酶(MMP - 2和9)以及细胞周期检查点蛋白(细胞周期蛋白D1)的水平,来评价香草酸(一种生物类黄酮)对甲基硝基亚硝基胍(MNNG)诱导的致癌大鼠子宫内膜癌(EC)的化学预防效果。MNNG(150 mg/kg体重,持续90天)经阴道留置诱发的EC,导致TBARS、LOOH、细胞色素P450水平升高,抗氧化剂(SOD、CAT、GPx、GSH、维生素C和E)水平降低,且MMP - 2和9以及细胞周期蛋白D1的表达上调(通过蛋白质免疫印迹分析)。对经MNNG处理的大鼠给予香草酸(100 mg/kg体重)治疗:(1)使组织病理学改变恢复正常;(2)降低TBARS、LOOH和细胞色素P450的水平;(3)提高血浆和子宫中抗氧化剂(SOD、CAT、GPx、GSH、维生素C和E)的水平;(4)下调MMP - 2、9和细胞周期蛋白D1的表达。香草酸在预处理组中的作用比联合治疗组的大鼠更为显著。我们的结果表明,香草酸通过提高抗氧化剂水平以及调节金属蛋白酶和细胞周期检查点蛋白的水平来抑制子宫内膜癌。

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