Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center at Omaha, Omaha, Nebraska.
Department of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, Florida.
Gastroenterology. 2024 Oct;167(5):867-884. doi: 10.1053/j.gastro.2024.05.005. Epub 2024 May 15.
Gastrointestinal (GI) cancers are the leading cause of new cancer cases and cancer-related deaths worldwide. The treatment strategies for patients with GI tumors have focused on oncogenic molecular profiles associated with tumor cells. Recent evidence has demonstrated that the tumor cell functions are modulated by its microenvironment, compromising fibroblasts, extracellular matrices, microbiome, immune cells, and the enteric nervous system. Along with the tumor microenvironment components, alterations in key metabolic pathways have emerged as a hallmark of tumor cells. From these perspectives, this review will highlight the functions of different cellular components of the GI tumor microenvironment and their implications for treatment. Furthermore, we discuss the major metabolic reprogramming in GI tumor cells and how understanding metabolic rewiring could lead to new therapeutic strategies. Finally, we briefly summarize the targeted agents currently being studied in GI cancers. Understanding the complex interplay between tumor cell-intrinsic and -extrinsic factors during tumor progression is critical for developing new therapeutic strategies.
胃肠道(GI)癌症是全球新癌症病例和癌症相关死亡的主要原因。GI 肿瘤患者的治疗策略集中于与肿瘤细胞相关的致癌分子特征。最近的证据表明,肿瘤细胞的功能受到其微环境的调节,包括成纤维细胞、细胞外基质、微生物组、免疫细胞和肠神经系统。除了肿瘤微环境成分外,关键代谢途径的改变也成为肿瘤细胞的一个标志。从这些角度来看,本综述将强调 GI 肿瘤微环境中不同细胞成分的功能及其对治疗的意义。此外,我们还讨论了 GI 肿瘤细胞中主要的代谢重编程,以及了解代谢重编程如何导致新的治疗策略。最后,我们简要总结了目前正在 GI 癌症中研究的靶向药物。了解肿瘤进展过程中肿瘤细胞内在和外在因素之间的复杂相互作用对于开发新的治疗策略至关重要。