Department of Biochemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
Department of Biochemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland.
Nutr Res. 2024 Jul;127:133-143. doi: 10.1016/j.nutres.2024.05.007. Epub 2024 Jun 3.
Colorectal cancer (CRC) is one of the leading causes of cancer-related death. Currently, dietary factors are being emphasized in the pathogenesis of CRC. There is strong evidence that fatty acids (FAs) and free FA receptors (FFARs) are involved in CRC. This comprehensive review discusses the role of FAs and their receptors in CRC pathophysiology, development, and treatment. In particular, butyrate and n-3 polyunsaturated fatty acids have been found to exert anticancer properties by, among others, inhibiting proliferation and metastasis and inducing apoptosis in tumor cells. Consequently, they are used in conjunction with conventional therapies. Furthermore, FFAR gene expression is down-regulated in CRC, suggesting their suppressive character. Recent studies showed that the FFAR4 agonist, GW9508, can inhibit tumor growth. In conclusion, natural as well as synthetic FFAR ligands are considered promising candidates for CRC therapy.
结直肠癌(CRC)是癌症相关死亡的主要原因之一。目前,饮食因素在 CRC 的发病机制中受到重视。有强有力的证据表明脂肪酸(FAs)和游离脂肪酸受体(FFARs)参与了结直肠癌的发生发展和治疗。本综述讨论了 FAs 及其受体在 CRC 病理生理学、发展和治疗中的作用。特别是丁酸和 n-3 多不饱和脂肪酸已被发现通过抑制肿瘤细胞的增殖和转移以及诱导细胞凋亡来发挥抗癌作用。因此,它们与传统疗法联合使用。此外,CRC 中 FFAR 基因表达下调,提示其抑制作用。最近的研究表明,FFAR4 激动剂 GW9508 可以抑制肿瘤生长。总之,天然和合成的 FFAR 配体被认为是 CRC 治疗的有前途的候选药物。