Demir Kübra, Turgut Rana, Şentürk Selcen, Işıklar Handan, Günalan Elif
Institute of Graduate Education Istanbul Health and Technology University Istanbul Türkiye.
Faculty of Health Science, Department of Nutrition and Dietetics Sabahattin Zaim University Istanbul Türkiye.
Food Sci Nutr. 2024 Nov 7;12(12):9951-9973. doi: 10.1002/fsn3.4534. eCollection 2024 Dec.
Understanding the molecular signaling pathways of colorectal cancer (CRC) can be accepted as the first step in treatment strategy. Permanent mTOR signaling activation stimulates the CRC process via various biological processes. It supplies the survival of CRC stem cells, tumorigenesis, morbidity, and decreased response to drugs in CRC pathogenesis. Therefore, inhibition of the mTOR signaling by numerous bioactive components may be effective against CRC. The study aims to discuss the therapeutic capacity of various polyphenols, terpenoids, and alkaloids on CRC via the PI3K/Akt/mTOR pathway. The potential molecular effects of bioactive compounds on the mTOR pathway's upstream and downstream targets are examined. Each bioactive component causes various physiological processes, such as triggering free radical production, disruption of mitochondrial membrane potential, cell cycle arrest, inhibition of CRC stem cell migration, and suppression of glycolysis through mTOR signaling inhibition. As a result, carcinogenesis is inhibited by inducing apoptosis and autophagy. However, it should be noted that studies are primarily in vitro dose-dependent treatment researchers. This study raises awareness about the role of phenolic compounds in treating CRC, contributing to their future use as anticancer agents. These bioactive compounds have the potential to be developed into food supplementation to prevent and treat various cancer types including CRC. This review has the potential to lead to further development of clinical studies. In the future, mTOR inhibition by applying several bioactive agents using advanced drug delivery systems may contribute to CRC treatment with 3D cell culture and in vivo clinical studies.
了解结直肠癌(CRC)的分子信号通路可被视为治疗策略的第一步。mTOR信号通路的持续激活通过各种生物学过程刺激CRC进程。它在CRC发病机制中为CRC干细胞的存活、肿瘤发生、发病率及对药物反应的降低提供支持。因此,多种生物活性成分对mTOR信号通路的抑制可能对CRC有效。本研究旨在探讨各种多酚、萜类和生物碱通过PI3K/Akt/mTOR途径对CRC的治疗能力。研究了生物活性化合物对mTOR通路上下游靶点的潜在分子效应。每种生物活性成分都会引发各种生理过程,如触发自由基产生、破坏线粒体膜电位、细胞周期停滞、抑制CRC干细胞迁移以及通过抑制mTOR信号通路抑制糖酵解。结果,通过诱导凋亡和自噬来抑制致癌作用。然而,应该注意的是,研究主要是体外剂量依赖性治疗研究。本研究提高了人们对酚类化合物在治疗CRC中作用的认识,有助于它们未来用作抗癌剂。这些生物活性化合物有潜力开发成食品补充剂,用于预防和治疗包括CRC在内的各种癌症类型。本综述有可能推动临床研究的进一步发展。未来,使用先进的药物递送系统应用多种生物活性剂抑制mTOR可能有助于通过3D细胞培养和体内临床研究来治疗CRC。