Wang Haitao, Tang Rui, Jiang Ling, Jia Yingtian
The School of Clinical Medical Sciences, Southwest Medical University, Luzhou, Sichuan, China.
Chengdu Anorectal Hospital, Chengdu, China.
Front Pharmacol. 2024 Oct 30;15:1494802. doi: 10.3389/fphar.2024.1494802. eCollection 2024.
PIK3CA gene encodes the p110α catalytic subunit of PI3K, which regulates the PI3K/AKT/mTOR signaling pathway. PIK3CA gene mutation is one of the most common mutations in colorectal cancer (CRC), affecting about 15%-20% of CRC patients. PIK3CA gene mutation leads to the persistent activation of the PI3K/AKT/mTOR signaling pathway, which promotes the proliferation, invasion, metastasis, and drug resistance of CRC. This article provides a summary of the key detection methods for PIK3CA gene mutation, and provides an introduction to the existing colorectal cancer treatments and their practical applications in the clinic. Besides, this article summarizes the role and mechanism of PIK3CA gene mutation in the occurrence and development of CRC. It also explores the relationship between PIK3CA gene mutation and the clinical features and prognosis of CRC. This article focuses on the influence and mechanism of PIK3CA gene mutation on the targeted therapy and immunotherapy of CRC, and discusses the potential value and future direction of PIK3CA gene mutation in the personalized therapy of CRC. We aim to provide new perspectives and ideas for the precise diagnosis and treatment of CRC.
PIK3CA基因编码PI3K的p110α催化亚基,该亚基调节PI3K/AKT/mTOR信号通路。PIK3CA基因突变是结直肠癌(CRC)中最常见的突变之一,约15%-20%的CRC患者受其影响。PIK3CA基因突变导致PI3K/AKT/mTOR信号通路持续激活,促进CRC的增殖、侵袭、转移及耐药。本文总结了PIK3CA基因突变的关键检测方法,并介绍了现有的结直肠癌治疗方法及其在临床中的实际应用。此外,本文总结了PIK3CA基因突变在CRC发生发展中的作用及机制,还探讨了PIK3CA基因突变与CRC临床特征及预后的关系。本文重点关注PIK3CA基因突变对CRC靶向治疗和免疫治疗的影响及机制,并讨论PIK3CA基因突变在CRC个体化治疗中的潜在价值和未来方向。我们旨在为CRC的精准诊断和治疗提供新的视角和思路。