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基于肠促胰岛素的疗法与癌症:有哪些新进展?

Incretin-Based Therapies and Cancer: What's New?

作者信息

Medenica Sanja, Bogdanovic Jelena, Vekic Jelena, Vojinovic Tanja, Babic Ivana, Bogdanović Ljiljana, Maggio Viviana, Tanani Mohamed El, Rizzo Manfredi

机构信息

Department of Endocrinology, Internal Medicine Clinic, Clinical Centre of Montenegro, 81000 Podgorica, Montenegro.

Faculty of Medicine, University of Montenegro, 81000 Podgorica, Montenegro.

出版信息

Medicina (Kaunas). 2025 Apr 7;61(4):678. doi: 10.3390/medicina61040678.

Abstract

Growing interest in incretin-based therapies for diabetes mellitus has led to an increased evaluation of their potential effects on cancer development. This review aims to synthesize recent evidence regarding the relationship between incretin-based therapies and cancer risk. We conducted a comprehensive literature review focusing on studies investigating dipeptidyl peptidase-4 (DPP-4) inhibitors, glucagon-like peptide-1 (GLP-1) receptor agonists, and dual GLP-1/glucose-dependent insulinotropic polypeptide (GIP) receptor agonists in relation to various malignancies. Current findings suggest that while these therapies demonstrate potential benefits, including weight reduction and metabolic regulation, concerns remain regarding their long-term safety profile. Notably, some studies indicate an increased risk of thyroid and pancreatic cancers, while others report protective effects against prostate, colorectal, and breast cancers. Given the complexity of their effects, further long-term studies and post-marketing surveillance are warranted. This review highlights the need for careful clinical assessment when prescribing incretin-based therapies to patients who may be at increased risk of cancer.

摘要

对基于肠促胰岛素的糖尿病治疗方法的兴趣日益浓厚,这导致人们对其在癌症发展方面潜在影响的评估有所增加。本综述旨在综合有关基于肠促胰岛素的治疗方法与癌症风险之间关系的最新证据。我们进行了一项全面的文献综述,重点关注研究二肽基肽酶-4(DPP-4)抑制剂、胰高血糖素样肽-1(GLP-1)受体激动剂以及双重GLP-1/葡萄糖依赖性促胰岛素多肽(GIP)受体激动剂与各种恶性肿瘤关系的研究。目前的研究结果表明,虽然这些治疗方法显示出潜在益处,包括体重减轻和代谢调节,但人们仍对其长期安全性表示担忧。值得注意的是,一些研究表明甲状腺癌和胰腺癌的风险增加,而另一些研究则报告对前列腺癌、结直肠癌和乳腺癌有保护作用。鉴于其影响的复杂性,有必要进行进一步的长期研究和上市后监测。本综述强调,在为可能患癌风险增加的患者开基于肠促胰岛素的治疗药物时,需要进行仔细的临床评估。

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