茚并[1,2-d]噻唑并[3,2-a]嘧啶类似物对 IL-6 介导的 STAT3 的抗增殖作用以及氨基甲酸乙酯诱导的白化 Wistar 大鼠肺癌细胞凋亡途径的作用:硅内、体外和体内研究。

IF 5.3 2区 医学 Q1 ONCOLOGY
Archana Bharti Sonkar, Abhishek Verma, Sneha Yadav, Rohit Kumar, Jyoti Singh, Amit K Keshari, Soniya Rani, Anurag Kumar, Dharmendra Kumar, Neeraj Kumar Shrivastava, Shubham Rastogi, Mariam K Alamoudi, Mohd Nazam Ansari, Abdulaziz S Saeedan, Gaurav Kaithwas, Sudipta Saha
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引用次数: 0

摘要

肺癌(LC)在女性癌症发病率中仅次于乳腺癌,在男性癌症发病率中仅次于前列腺癌。根据 GLOBOCAN 2020 报告,印度占肺癌病例的 5.9%,占肺癌死亡人数的 8.1%。多项临床研究表明,乳腺癌的发生是由于生物学和形态学异常,以及抗氧化剂、细胞因子和细胞凋亡标志物水平的改变。在本研究中,我们采用体外、硅内和体内模型,探讨了茚并[1,2-d]噻唑并[3,2-a]嘧啶类似物对 LC 的抗增殖活性。针对 A549 细胞的体外筛选显示,化合物 9B (8-甲氧基-5-(3,4,5-三甲氧基苯基)-5,6-二氢茚并[1,2-d]噻唑并[3,2-a]嘧啶)和 12B (5-(4-氯苯基)-5,6-二氢茚并[1,2-d]噻唑并[3,2-a]嘧啶)是抗 LC 的潜在嘧啶类似物。使用 AutoDock Vina 4.1 将化合物 9B 和 12B 与不同的分子靶标 IL-6、Cyt-C、Caspase9 和 Caspase3 进行对接,以评估其结合亲和力。随后,在白化 Wistar 大鼠体内通过氨基甲酸乙酯(EC)诱导 LC 进行了体内研究。9B 和 12B 对白化 Wistar 大鼠在氨基甲酸乙酯诱导的 LC 中的生理指标(体重变化)、生化指标(抗氧化剂 [TBAR、SOD、ProC 和 GSH]、血脂指标(TC、TG、LDL、VLDL 和 HDL)]和细胞因子指标(IL-2、IL-6、IL-10 和 IL-1β)均有显著影响。形态学检查(SEM和H&E)和Western印迹(IL-6、STAT3、Cyt-C、BAX、Bcl-2、Caspase3和caspase9)表明,化合物9B和12B具有抗增殖作用。因此,从体外、硅内和体内实验结果来看,我们认为 9B 和 12B 具有显著的抗增殖潜力,是进一步评估的潜在候选化合物,以满足新药申请研究的要求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antiproliferative effect of indeno[1,2-d]thiazolo[3,2-a]pyrimidine analogues on IL-6 mediated STAT3 and role of the apoptotic pathway in albino Wistar rats of ethyl carbamate-induced lung carcinoma: In-silico, In-vitro, and In-vivo study.

Lung cancer (LC) ranks second most prevalent cancer in females after breast cancer and second in males after prostate cancer. Based on the GLOBOCAN 2020 report, India represented 5.9% of LC cases and 8.1% of deaths caused by the disease. Several clinical studies have shown that LC occurs because of biological and morphological abnormalities and the involvement of altered level of antioxidants, cytokines, and apoptotic markers. In the present study, we explored the antiproliferative activity of indeno[1,2-d]thiazolo[3,2-a]pyrimidine analogues against LC using in-vitro, in-silico, and in-vivo models. In-vitro screening against A549 cells revealed compounds 9B (8-methoxy-5-(3,4,5-trimethoxyphenyl)-5,6-dihydroindeno[1,2-d]thiazolo[3,2-a]pyrimidine) and 12B (5-(4-chlorophenyl)-5,6-dihydroindeno[1,2-d]thiazolo[3,2-a]pyrimidine) as potential pyrimidine analogues against LC. Compounds 9B and 12B were docked with different molecular targets IL-6, Cyt-C, Caspase9, and Caspase3 using AutoDock Vina 4.1 to evaluate the binding affinity. Subsequently, in-vivo studies were conducted in albino Wistar rats through ethyl-carbamate (EC)- induced LC. 9B and 12B imparted significant effects on physiological (weight variation), and biochemical (anti-oxidant [TBAR's, SOD, ProC, and GSH), lipid (TC, TG, LDL, VLDL, and HDL)], and cytokine (IL-2, IL-6, IL-10, and IL-1β) markers in EC-induced LC in albino Wistar rats. Morphological examination (SEM and H&E) and western blotting (IL-6, STAT3, Cyt-C, BAX, Bcl-2, Caspase3, and caspase9) showed that compounds 9B and 12B had antiproliferative effects. Accordingly, from the in-vitro, in-silico, and in-vivo experimental findings, we concluded that 9B and 12B have significant antiproliferative potential and are potential candidates for further evaluation to meet the requirements of investigation of new drug application.

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来源期刊
CiteScore
10.90
自引率
1.70%
发文量
360
审稿时长
1 months
期刊介绍: Cancer Cell International publishes articles on all aspects of cancer cell biology, originating largely from, but not limited to, work using cell culture techniques. The journal focuses on novel cancer studies reporting data from biological experiments performed on cells grown in vitro, in two- or three-dimensional systems, and/or in vivo (animal experiments). These types of experiments have provided crucial data in many fields, from cell proliferation and transformation, to epithelial-mesenchymal interaction, to apoptosis, and host immune response to tumors. Cancer Cell International also considers articles that focus on novel technologies or novel pathways in molecular analysis and on epidemiological studies that may affect patient care, as well as articles reporting translational cancer research studies where in vitro discoveries are bridged to the clinic. As such, the journal is interested in laboratory and animal studies reporting on novel biomarkers of tumor progression and response to therapy and on their applicability to human cancers.
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