Malopolska Centre of Biotechnology, Jagiellonian University, ul. Gronostajowa 7A, 30-387 Krakow, Poland.
Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, ul. Gronostajowa 7, 30-387 Krakow, Poland.
Int J Mol Sci. 2020 May 1;21(9):3218. doi: 10.3390/ijms21093218.
Pancreatic ductal adenocarcinoma (PDAC) causes annually well over 400,000 deaths world-wide and remains one of the major unresolved health problems. This exocrine pancreatic cancer originates from the mutated epithelial cells: acinar and ductal cells. However, the epithelia-derived cancer component forms only a relatively small fraction of the tumor mass. The majority of the tumor consists of acellular fibrous stroma and diverse populations of the non-neoplastic cancer-associated cells. Importantly, the tumor microenvironment is maintained by dynamic cell-cell and cell-matrix interactions. In this article, we aim to review the most common drivers of PDAC. Then we summarize the current knowledge on PDAC microenvironment, particularly in relation to pancreatic cancer therapy. The focus is placed on the acellular stroma as well as cell populations that inhabit the matrix. We also describe the altered metabolism of PDAC and characterize cellular signaling in this cancer.
胰腺导管腺癌(PDAC)每年在全球导致超过 40 万人死亡,仍然是未解决的主要健康问题之一。这种外分泌胰腺癌症来源于突变的上皮细胞:腺泡细胞和导管细胞。然而,上皮来源的癌症成分仅占肿瘤质量的相对较小部分。肿瘤的大部分由无细胞纤维基质和多种非肿瘤相关的细胞组成。重要的是,肿瘤微环境是通过动态的细胞-细胞和细胞-基质相互作用维持的。在本文中,我们旨在综述 PDAC 的最常见驱动因素。然后,我们总结了目前关于 PDAC 微环境的知识,特别是与胰腺癌治疗相关的知识。重点放在无细胞基质以及居住在基质中的细胞群体上。我们还描述了 PDAC 的改变代谢,并描述了这种癌症中的细胞信号转导。