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拉卡酸和苯乙基异硫氰酸酯联合通过双重抑制 DNA 甲基转移酶-1 和组蛋白去乙酰化酶-1 在结直肠癌中的抗肿瘤活性。

Potent antitumor activity of Laccaic acid and Phenethyl isothiocyanate combination in colorectal cancer via dual inhibition of DNA methyltransferase-1 and Histone deacetylase-1.

机构信息

Department of Pharmacology, SVKM's Dr. Bhanuben Nanavati College of Pharmacy, Vile Parle (W), Mumbai, India.

Department of Pharmacology, SVKM's Dr. Bhanuben Nanavati College of Pharmacy, Vile Parle (W), Mumbai, India.

出版信息

Toxicol Appl Pharmacol. 2019 Aug 15;377:114631. doi: 10.1016/j.taap.2019.114631. Epub 2019 Jun 19.

Abstract

Despite an incessant advancement in the treatment of Colorectal Cancer (CRC), 40% of individuals suffer from disease relapse which marks the need for new treatment options. In this study we report synergistic antitumor activity of Laccaic acid (LA) and Phenethyl isothiocyanate (PEITC) combination in colorectal cancer via dual inhibition of DNA methyltransferase-1 and Histone deacetylase-1. Efficacy of combination was evaluated in both in-vitro and in-vivo experiments using human colon carcinoma cell line HT29 and 1,2-dimethyl hydrazine induced colon cancer rat model, respectively. In the cell line studies treatment with combination showed reduced cell viability with apoptotic cell death compared to individual treatment groups which showed necrotic cell death. IC50 value for combination (0.478 μM) was much lower than LA (6.08 μM), PEITC (11.88 μM) and 5-Fluorouracil (9.88 μM). In the in-vivo study combination group significantly attenuated number of aberrant crypt foci, fecal consistency score, IL-6, TNF-α, DNMT1 and HDAC1 levels, histological findings and mortality as compared to negative control. Further, toxic effects produced by combination were significantly less. Results suggest potent synergistic efficacy of Laccaic acid and Phenethyl isothiocyanate combination in colorectal cancer.

摘要

尽管在结直肠癌(CRC)的治疗方面取得了持续的进展,但仍有 40%的患者出现疾病复发,这标志着需要新的治疗选择。在这项研究中,我们报告了通过双重抑制 DNA 甲基转移酶-1 和组蛋白去乙酰化酶-1,漆酚酸(LA)和苯乙基异硫氰酸酯(PEITC)联合在结直肠癌中的协同抗肿瘤活性。使用人结肠癌细胞系 HT29 和 1,2-二甲基肼诱导的结肠癌大鼠模型,分别在体外和体内实验中评估了联合治疗的疗效。在细胞系研究中,与单独治疗组相比,联合治疗组表现出降低的细胞活力和凋亡性细胞死亡,而单独治疗组表现出坏死性细胞死亡。联合治疗的 IC50 值(0.478μM)远低于 LA(6.08μM)、PEITC(11.88μM)和 5-氟尿嘧啶(9.88μM)。在体内研究中,与阴性对照组相比,联合组显著减少了异常隐窝病灶、粪便稠度评分、IL-6、TNF-α、DNMT1 和 HDAC1 水平、组织学发现和死亡率。此外,联合治疗产生的毒性作用明显较小。结果表明,漆酚酸和苯乙基异硫氰酸酯联合在结直肠癌中有很强的协同疗效。

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