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结直肠癌的临床前药物发现:以天然化合物为重点。

Preclinical Drug Discovery in Colorectal Cancer: A Focus on Natural Compounds.

机构信息

Department of Physiology, College of Medicine, University of Sulaimani, 46001 Sulaymaniyah, Iraq.

Department of Medical Laboratory Sciences, Komar University of Science and Technology, Chaq-Chaq Qularaisee, Sulaimaniyah, Iraq

出版信息

Curr Drug Targets. 2021;22(9):977-997. doi: 10.2174/1389450122666210405105206.

Abstract

BACKGROUND

Colorectal cancer (CRC) is considered one of the most predominant and deadly cancer globally. Nowadays, the main clinical management for this cancer includes chemotherapy and surgery; however, these treatments result in the occurrence of drug resistance and severe side effects, and thus it is a crucial requirement to discover an alternative and potential therapy for CRC treatment. Numerous therapeutic cancers were initially recognized from natural metabolites utilized in traditional medicine, and several recent types of research have shown that many natural products own potential effects against CRC and may assist the action of chemotherapy for the treatment of CRC. It has been indicated that most patients are well tolerated by natural compounds without showing any toxicity signs even at high doses. Conventional chemotherapeutics interaction with natural medicinal compounds presents a new feature in cancer exploration and treatment. Most of the natural compounds overwhelm malignant cell propagation by apoptosis initiation of CRC cells and arresting of the cell cycle (especially at G, S, and G2/M phase) that result in inhibition of tumor growth.

OBJECTIVE

This mini-review aimed to focus on natural compounds (alkaloids, flavonoids, polysaccharides, polyphenols, terpenoids, lactones, quinones, etc.) that were identified to have anti- CRC activity in vitro on CRC cell lines and/or in vivo experiments on animal models.

CONCLUSION

Most of the studied active natural compounds possess anti-CRC activity via different mechanisms and pathways in vitro and in vivo that might be used as assistance by clinicians to support chemotherapy therapeutic strategy and treatment doses for cancer patients.

摘要

背景

结直肠癌(CRC)被认为是全球最主要和最致命的癌症之一。目前,这种癌症的主要临床治疗方法包括化疗和手术;然而,这些治疗方法会导致耐药性和严重的副作用的发生,因此,寻找一种替代和潜在的 CRC 治疗方法是至关重要的。许多治疗癌症的药物最初都是从传统医学中使用的天然代谢物中发现的,最近的一些研究表明,许多天然产物对 CRC 具有潜在的作用,并可能有助于化疗治疗 CRC。已经表明,大多数患者对天然化合物的耐受性良好,即使在高剂量下也没有表现出任何毒性迹象。传统化疗药物与天然药物化合物的相互作用为癌症的探索和治疗带来了新的特点。大多数天然化合物通过诱导 CRC 细胞凋亡和细胞周期停滞(特别是在 G、S 和 G2/M 期)来抑制肿瘤生长,从而抑制恶性细胞的增殖。

目的

本综述旨在重点介绍在 CRC 细胞系的体外实验和动物模型的体内实验中被鉴定出具有抗 CRC 活性的天然化合物(生物碱、类黄酮、多糖、多酚、萜类、内酯、醌等)。

结论

大多数研究的活性天然化合物通过不同的机制和途径在体外和体内具有抗 CRC 活性,这可能被临床医生用作辅助手段,以支持癌症患者的化疗治疗策略和治疗剂量。

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