天然化合物作为胰腺癌的潜在治疗药物:综述。

IF 1.8 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xing-Da Lin, Tian Li, Rui-Xia Du, Gui-Chen Li, Zhe Liu
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引用次数: 0

摘要

胰腺癌是一种高致死率的恶性肿瘤,5年生存率低。本文就天然化合物作为潜在的治疗药物进行综述。不同类型的天然化合物,如多酚、皂苷和生物碱,已经显示出抗胰腺癌的作用,包括抑制肿瘤细胞生长、诱导细胞凋亡和防止血管生成。它们还通过影响肠道微生物群、糖脂代谢和内分泌系统对胰腺癌产生间接影响。此外,含有这些化合物的中草药在临床应用中显示出前景。然而,诸如目标识别和低生物利用度等挑战仍然存在。未来的研究趋势包括跨学科合作和使用先进技术来克服这些问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Natural Compounds as Potential Therapeutics for Pancreatic Cancer: A Narrative Review.

Pancreatic cancer is a highly lethal malignancy with a low 5-year survival rate. This review fo-cuses on natural compounds as potential therapeutics for it. Different types of natural compounds, such as polyphenols, saponins, and alkaloids, have shown anti-pancreatic cancer effects, including inhibiting tumor cell growth, inducing apoptosis, and preventing angiogenesis. They also have indirect impacts on pancreatic cancer through influencing the gut microbiota, glucose and lipid metabolism, and the endocrine system. Ad-ditionally, Chinese herbal medicines containing these compounds show promise in clinical applications. However, challenges such as target identification and low bioavailability persist. Future research trends in-volve interdisciplinary collaboration and the use of advanced technologies to overcome these issues.

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来源期刊
Current drug metabolism
Current drug metabolism 医学-生化与分子生物学
CiteScore
4.30
自引率
4.30%
发文量
81
审稿时长
4-8 weeks
期刊介绍: Current Drug Metabolism aims to cover all the latest and outstanding developments in drug metabolism, pharmacokinetics, and drug disposition. The journal serves as an international forum for the publication of full-length/mini review, research articles and guest edited issues in drug metabolism. Current Drug Metabolism is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the most important developments. The journal covers the following general topic areas: pharmaceutics, pharmacokinetics, toxicology, and most importantly drug metabolism. More specifically, in vitro and in vivo drug metabolism of phase I and phase II enzymes or metabolic pathways; drug-drug interactions and enzyme kinetics; pharmacokinetics, pharmacokinetic-pharmacodynamic modeling, and toxicokinetics; interspecies differences in metabolism or pharmacokinetics, species scaling and extrapolations; drug transporters; target organ toxicity and interindividual variability in drug exposure-response; extrahepatic metabolism; bioactivation, reactive metabolites, and developments for the identification of drug metabolites. Preclinical and clinical reviews describing the drug metabolism and pharmacokinetics of marketed drugs or drug classes.
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