Li Jin-Tao, Lei Ming-Zhu, Lei Qun-Ying, Yin Miao
Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, China.
Sichuan Da Xue Xue Bao Yi Xue Ban. 2021 Jan;52(1):5-10. doi: 10.12182/20210160502.
Pancreatic ductal adenocarcinoma (PDAC) is one of the most notorious malignancies with a 5-year survival rate of less than 8%. Therefore, it is crucial to investigate the molecular mechanism underlining PDAC initiation, promotion, and progression for efficient treatment of PDAC. In order to adapt and survive in an extremely adverse microenvironment of hypoxia and insufficiency of nutrients and energy, PDAC cells undergo extensive metabolic modification triggered by intrinsic signalings which are activated by different genetic events, including mutations occurred at , 53, and 4/ 4, collaboratively promoting PDAC development. Notably, PDCA cells have extensive crosstalk in the form of reciprocal metabolic flux with its surrounding microenvironment to facilitate tumor advancement and therapy resistance. We herein summarize recent findings of PDAC metabolism and discuss metabolic rewiring-based therapeutic strategies.
胰腺导管腺癌(PDAC)是最臭名昭著的恶性肿瘤之一,5年生存率低于8%。因此,研究PDAC发生、发展和进展的分子机制对于有效治疗PDAC至关重要。为了在缺氧以及营养和能量不足的极端不利微环境中适应和生存,PDAC细胞会经历由内在信号触发的广泛代谢改变,这些内在信号由不同的基因事件激活,包括发生在 、53和4/ 4的突变,共同促进PDAC的发展。值得注意的是,PDCA细胞与其周围微环境以相互代谢通量的形式存在广泛的串扰,以促进肿瘤进展和治疗抗性。我们在此总结了PDAC代谢的最新发现,并讨论了基于代谢重塑的治疗策略。