Li Jin-Tao, Wang Yi-Ping, Yin Miao, Lei Qun-Ying
Fudan University Shanghai Cancer Center and Cancer Metabolism Laboratory, Institutes of Biomedical Sciences, Shanghai Medical College, Fudan University; Department of Oncology, Shanghai Medical College, Fudan University, Shanghai 200032, People's Republic of China.
Lead Contact.
Cell Stress. 2019 Nov 4;3(12):361-368. doi: 10.15698/cst2019.12.205.
Pancreatic ductal adenocarcinoma (PDAC) is predicted to become the second leading cause of death of patients with malignant cancers by 2030. Current options of PDAC treatment are limited and the five-year survival rate is less than 8%, leading to an urgent need to explore innovatively therapeutic strategies. PDAC cells exhibit extensively reprogrammed metabolism to meet their energetic and biomass demands under extremely harsh conditions. The metabolic changes are closely linked to signaling triggered by activation of oncogenes like as well as inactivation of tumor suppressors. Furthermore, tumor microenvironmental factors including extensive desmoplastic stroma reaction result in series of metabolism remodeling to facilitate PDAC development. In this review, we focus on the dysregulation of metabolism in PDAC and its surrounding microenvironment to explore potential metabolic targets in PDAC therapy.
预计到2030年,胰腺导管腺癌(PDAC)将成为恶性肿瘤患者的第二大死因。目前PDAC的治疗选择有限,五年生存率低于8%,因此迫切需要探索创新的治疗策略。PDAC细胞在极其恶劣的条件下表现出广泛的代谢重编程,以满足其能量和生物量需求。这些代谢变化与癌基因激活以及肿瘤抑制因子失活所触发的信号密切相关。此外,包括广泛的促结缔组织增生性基质反应在内的肿瘤微环境因素会导致一系列代谢重塑,以促进PDAC的发展。在这篇综述中,我们聚焦于PDAC及其周围微环境中的代谢失调,以探索PDAC治疗中的潜在代谢靶点。