Centre de Recherche en Cancérologie de Marseille (CRCM), INSERM U1068, CNRS UMR 7258, Aix-Marseille Université and Institut Paoli-Calmettes, Parc Scientifique et Technologique de Luminy, 163 Avenue de Luminy, 13288 Marseille, France.
Int J Mol Sci. 2021 May 7;22(9):4970. doi: 10.3390/ijms22094970.
Pancreatic fibrosis is caused by the excessive deposits of extracellular matrix (ECM) and collagen fibers during repeated necrosis to repair damaged pancreatic tissue. Pancreatic fibrosis is frequently present in chronic pancreatitis (CP) and pancreatic cancer (PC). Clinically, pancreatic fibrosis is a pathological feature of pancreatitis and pancreatic cancer. However, many new studies have found that pancreatic fibrosis is involved in the transformation from pancreatitis to pancreatic cancer. Thus, the role of fibrosis in the crosstalk between pancreatitis and pancreatic cancer is critical and still elusive; therefore, it deserves more attention. Here, we review the development of pancreatic fibrosis in inflammation and cancer, and we discuss the therapeutic strategies for alleviating pancreatic fibrosis. We further propose that cellular stress response might be a key driver that links fibrosis to cancer initiation and progression. Therefore, targeting stress proteins, such as nuclear protein 1 (NUPR1), could be an interesting strategy for pancreatic fibrosis and PC treatment.
胰腺纤维化是由反复坏死修复受损胰腺组织过程中细胞外基质(ECM)和胶原纤维的过度沉积引起的。胰腺纤维化在慢性胰腺炎(CP)和胰腺癌(PC)中很常见。临床上,胰腺纤维化是胰腺炎和胰腺癌的病理特征。然而,许多新的研究发现,胰腺纤维化参与了胰腺炎向胰腺癌的转化。因此,纤维化在胰腺炎和胰腺癌相互作用中的作用至关重要,但仍不清楚;因此,它值得更多关注。在这里,我们综述了炎症和癌症中胰腺纤维化的发展,并讨论了缓解胰腺纤维化的治疗策略。我们进一步提出,细胞应激反应可能是将纤维化与癌症发生和进展联系起来的关键驱动因素。因此,针对应激蛋白,如核蛋白 1(NUPR1),可能是治疗胰腺纤维化和 PC 的一个有趣策略。