Department of Medical and Biological Sciences, The Catholic University of Korea, 14662 Bucheon, Republic of Korea.
Department of Biotechnology, The Catholic University of Korea, 14662 Bucheon, Republic of Korea.
Front Biosci (Landmark Ed). 2024 Apr 2;29(4):137. doi: 10.31083/j.fbl2904137.
Most pancreatic cancers are pancreatic ductal adenocarcinomas. This is an extremely lethal disease with poor prognosis and almost no treatment choices. Considering the profound role of the pancreas in the human body, malfunction of this organ can significantly affect quality of life. Although multiple metabolic pathways are altered in cancer cells, certain metabolic gene signatures may be critical for immunotherapy. The reprogrammed metabolism of glucose, amino acids, and lipids can nourish the tumor microenvironment (TME). Previous studies have also shown that reprogrammed metabolism influences immune responses. Tumor-infiltrating immune cells in the TME can adapt their metabolism to blunt the immune system, leading to immunosuppression and tumor progression. The identification of metabolism-related genes (MRGs) associated with immune reactions in pancreatic cancer may lead to improved treatments. This review highlights the characteristics of MRGs in pancreatic cancer and suggests that enhanced anti-cancer therapies could be used to overcome resistance to immunotherapy.
大多数胰腺癌是胰腺导管腺癌。这是一种预后极差、几乎没有治疗选择的极致命疾病。考虑到胰腺在人体中的重要作用,该器官的功能障碍会显著影响生活质量。尽管癌细胞中多个代谢途径发生改变,但某些代谢基因特征可能对免疫疗法至关重要。葡萄糖、氨基酸和脂质的重新编程代谢可以滋养肿瘤微环境(TME)。先前的研究还表明,重新编程的代谢会影响免疫反应。TME 中的肿瘤浸润免疫细胞可以调整其代谢以削弱免疫系统,导致免疫抑制和肿瘤进展。鉴定与胰腺癌免疫反应相关的代谢相关基因(MRGs)可能会导致治疗方法的改进。本综述强调了胰腺癌细胞中 MRGs 的特征,并提出增强抗癌疗法可用于克服免疫疗法的耐药性。