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舒林酸砜作为一种选择性凋亡抗肿瘤药物在人头颈部鳞状细胞癌细胞系中的化学预防功效:一项系统评价

Chemopreventive Efficacy of Sulindac Sulfone as a Selective Apoptotic Antineoplastic Drug in Human Head and Neck Squamous Cell Carcinoma Cell Lines: A Systematic Review.

作者信息

Karuppiah Nivethitha, B Sivapathasundharam, Chockalingam Rajeswari M, Bhupathy Prem Karthick, Kalaimani Gnanambigai, Ramamurthi Raghini

机构信息

Oral Pathology and Microbiology, Priyadarshini Dental College and Hospital, Tiruvallur, IND.

Oral and Maxillofacial Pathology, Priyadarshini Dental College and Hospital, Thiruvallur, IND.

出版信息

Cureus. 2024 Jan 5;16(1):e51692. doi: 10.7759/cureus.51692. eCollection 2024 Jan.

Abstract

Sulindac sulfone, an active metabolite of sulindac, a non-steroidal anti-inflammatory drug, has good anti-inflammatory potential. The antineoplastic effect of sulindac sulfone is mediated through a cyclooxygenase inhibitory mechanism, followed by apoptosis and inhibition of cell proliferation. Mounting studies have explored the anti-neoplastic effect of sulindac sulfone in various types of cancers in a dose-dependent manner. In this backdrop, we have conducted a systematic review to evaluate the efficacy and dose of sulindac sulfone as an anti-neoplastic agent in human head and neck squamous cell carcinoma cell lines (HNSCCs). In this study, we used a systematic literature review approach, and articles were searched in PubMed, and Medline with the keywords "sulindac sulfone," "anti-neoplastic activity," "chemopreventive," and "head and neck squamous cell carcinoma". A hand-search of journals was also performed. Articles were reviewed and analyzed. The analysis reveals that, based on the in vitro studies on various tumor models, the optimum concentration of sulindac sulfone which elicits anti-neoplastic effects is 200-800 µM. The anti-neoplastic effect is mediated through inhibition of cell proliferation and apoptosis. The results of our systematic review show that the anti-neoplastic activity of pharmacologic Sulindac sulfone is part of its dose-dependent activity, which can be safely employed in the therapy for human HNSCCs and would be responsible for a beneficial outcome of the treatment.

摘要

舒林酸砜是一种非甾体抗炎药舒林酸的活性代谢产物,具有良好的抗炎潜力。舒林酸砜的抗肿瘤作用是通过环氧化酶抑制机制介导的,随后诱导细胞凋亡并抑制细胞增殖。越来越多的研究已对舒林酸砜在各种类型癌症中的抗肿瘤作用进行了剂量依赖性研究。在此背景下,我们进行了一项系统评价,以评估舒林酸砜作为抗肿瘤药物在人头颈部鳞状细胞癌细胞系(HNSCCs)中的疗效和剂量。在本研究中,我们采用系统文献综述方法,在PubMed和Medline中搜索关键词为“舒林酸砜”、“抗肿瘤活性”、“化学预防”和“头颈部鳞状细胞癌”的文章。我们还对手检期刊进行了检索。对文章进行了审查和分析。分析表明,基于对各种肿瘤模型的体外研究,产生抗肿瘤作用的舒林酸砜最佳浓度为200 - 800µM。其抗肿瘤作用是通过抑制细胞增殖和诱导细胞凋亡介导的。我们的系统评价结果表明,药理学上的舒林酸砜的抗肿瘤活性是其剂量依赖性活性的一部分,可安全用于人类HNSCCs的治疗,并将带来有益的治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec61/10838484/c657830f04cb/cureus-0016-00000051692-i01.jpg

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