IN-SILICO ANALYSIS OF THYMOQUINONE AS AN ANTI-CANCER AGENT AGAINST CHEMORESISTANCE-ASSOCIATED PROTEINS IN OVARIAN CANCER

S. Tendulkar, Aishwarya Hattiholi, S. Dodamani
{"title":"IN-SILICO ANALYSIS OF THYMOQUINONE AS AN ANTI-CANCER AGENT AGAINST CHEMORESISTANCE-ASSOCIATED PROTEINS IN OVARIAN CANCER","authors":"S. Tendulkar, Aishwarya Hattiholi, S. Dodamani","doi":"10.55218/jasr.202314605","DOIUrl":null,"url":null,"abstract":"Thymoquinone (TQ), a polyphenol obtained from Nigella sativa plays a fundamental role in controlling homeostasis. Itpossesses anti-cancer, anti-oxidant, anti-inflammatory, and analgesic properties. Its anti-cancer properties extend tolymphoma, leukaemia, medulloblastoma, prostate, pancreatic, breast, and ovarian cancer (OvCa). OvCa is one of themost lethal malignancies worldwide having distinct symptoms and a poor prognosis. Resistance to Cisplatin (CDDP) andsubsequent reoccurrence of tumors lead to treatment failure. To tackle this, combination therapies along withpolyphenols are being studied and have been proven to enhance CDDP response. Certain proteins such as Bcl-2, Bax,STAT3, p53, and caspase-3/9 are involved in cancer progression and signaling of chemoresistance. In this study,Thymoquinone (TQ) interactions with these proteins have been observed through molecular docking. The 3D structureprediction was carried out using Phyre2 and SWISS-MODEL. The molecular docking of protein targets and TQ wasdone using the PatchDock server. The docked results were then visualized using Discovery Studio. This study helps us tounderstand the interactions between TQ and apoptotic proteins that help in the augmentation of conventional therapy.This knowledge will also help in developing a new approach and alternate therapeutic strategies using polyphenols likeTQ, even in resistant cells.","PeriodicalId":14906,"journal":{"name":"Journal of Advanced Scientific Research","volume":"8 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Advanced Scientific Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55218/jasr.202314605","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Thymoquinone (TQ), a polyphenol obtained from Nigella sativa plays a fundamental role in controlling homeostasis. Itpossesses anti-cancer, anti-oxidant, anti-inflammatory, and analgesic properties. Its anti-cancer properties extend tolymphoma, leukaemia, medulloblastoma, prostate, pancreatic, breast, and ovarian cancer (OvCa). OvCa is one of themost lethal malignancies worldwide having distinct symptoms and a poor prognosis. Resistance to Cisplatin (CDDP) andsubsequent reoccurrence of tumors lead to treatment failure. To tackle this, combination therapies along withpolyphenols are being studied and have been proven to enhance CDDP response. Certain proteins such as Bcl-2, Bax,STAT3, p53, and caspase-3/9 are involved in cancer progression and signaling of chemoresistance. In this study,Thymoquinone (TQ) interactions with these proteins have been observed through molecular docking. The 3D structureprediction was carried out using Phyre2 and SWISS-MODEL. The molecular docking of protein targets and TQ wasdone using the PatchDock server. The docked results were then visualized using Discovery Studio. This study helps us tounderstand the interactions between TQ and apoptotic proteins that help in the augmentation of conventional therapy.This knowledge will also help in developing a new approach and alternate therapeutic strategies using polyphenols likeTQ, even in resistant cells.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
胸腺醌作为一种抗癌剂对卵巢癌化疗耐药相关蛋白的作用的硅内分析
胸腺醌(TQ)是从黑麦草中提取的一种多酚,在控制体内平衡方面发挥着重要作用。它具有抗癌、抗氧化、抗炎和镇痛特性。其抗癌特性可用于淋巴瘤、白血病、髓母细胞瘤、前列腺癌、胰腺癌、乳腺癌和卵巢癌(OvCa)。卵巢癌是全球致死率最高的恶性肿瘤之一,症状明显,预后较差。对顺铂 (CDDP) 的耐药性和随后的肿瘤复发导致治疗失败。为了解决这个问题,人们正在研究与多酚一起使用的联合疗法,事实证明这种疗法可以增强 CDDP 的反应。某些蛋白质,如 Bcl-2、Bax、STAT3、p53 和 caspase-3/9 参与了癌症进展和化疗抗性信号的传递。本研究通过分子对接观察了胸腺醌(TQ)与这些蛋白的相互作用。使用 Phyre2 和 SWISS-MODEL 进行了三维结构预测。使用 PatchDock 服务器对目标蛋白质和 TQ 进行了分子对接。然后使用 Discovery Studio 对对接结果进行可视化。这项研究有助于我们理解 TQ 与凋亡蛋白之间的相互作用,从而有助于增强传统疗法。这些知识还将有助于开发新的方法,以及使用多酚(如 TQ)的替代治疗策略,即使是在耐药细胞中也是如此。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
A Review on Coronary Stents: With Polymers and without Polymers Evaluation of Neuroprotective effect of Bioactive compounds of Mucuna monosperma in PD lines of Drosophila melanogaster Formulation and Evaluation of Polyherbal Antidiabetic Capsules Contribution of Unani Physicians in Tashrīḥ al-Raḥim (Anatomy of the Uterus): A Systematic Review Isolation and Characterization of Rhizobacteria from Soil and Its Efficiency as Plant Growth- Promoting Microbes
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1