Wang Jian, Zhang Hui, Shao Peng, Zhang Xu, Zhou Bin
Department of General Surgery, Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research, The Affiliated Cancer Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, People's Republic of China.
Int J Gen Med. 2022 Mar 1;15:2311-2319. doi: 10.2147/IJGM.S350959. eCollection 2022.
Pancreatic adenocarcinoma has a poor prognosis and chemotherapy has its limitation due to tumor heterogeneity. It is essential to find novel targets involving in tumorigenesis of pancreatic adenocarcinoma. Growing evidences indicated that pyroptosis is involved in tumorigenesis of many cancers, but the relationship between pyroptosis and pancreatic adenocarcinoma still remains to be elucidated. Our object is to explore whether pyroptosis-related different expression genes have association with survivals of pancreatic adenocarcinoma patients and the mechanism they may participate in. Besides, we also analyzed their effect on immune cell infiltration in tumor microenvironment.
We used the bioinformatic analysis tool including GEPIA, cBioPortal, STRING, GeneMANIA, R software 4.03 and TIMER2.0 to investigate the different expression, prognostic value, protein-protein interaction, gene ontology, pathway and effect of immune cell infiltration of pyroptosis-related genes in PAAD.
Many pyroptosis-related genes express differently between pancreatic adenocarcinoma and normal tissues and they are associated with survival of PAAD. GABARAP and IL18 may play a key role in tumorigenesis of PAAD, for they are connected with overall survival, disease free survival and pathological stages at the same time. The function of pyroptosis-related genes includes cytokine production, endopeptidase activity, regulation of inflammation and inflammasome complex and pyroptosis-related genes have effect on immune cells infiltration in PAAD microenvironment.
Lots of pyroptosis-related DEGs may get involved in pathogenesis of PAAD and their high expression have an effect on survival. GABARAP and IL18 could be valuable research targets of PAAD.
胰腺腺癌预后较差,由于肿瘤异质性,化疗存在局限性。寻找参与胰腺腺癌肿瘤发生的新靶点至关重要。越来越多的证据表明,细胞焦亡参与多种癌症的肿瘤发生,但细胞焦亡与胰腺腺癌之间的关系仍有待阐明。我们的目的是探讨细胞焦亡相关差异表达基因是否与胰腺腺癌患者的生存率相关以及它们可能参与的机制。此外,我们还分析了它们对肿瘤微环境中免疫细胞浸润的影响。
我们使用了包括GEPIA、cBioPortal、STRING、GeneMANIA、R软件4.03和TIMER2.0在内的生物信息学分析工具,来研究胰腺腺癌中细胞焦亡相关基因的差异表达、预后价值、蛋白质-蛋白质相互作用、基因本体论、通路以及免疫细胞浸润的影响。
许多细胞焦亡相关基因在胰腺腺癌组织和正常组织之间表达不同,并且它们与胰腺腺癌的生存率相关。GABARAP和IL18可能在胰腺腺癌的肿瘤发生中起关键作用,因为它们同时与总生存期、无病生存期和病理分期相关。细胞焦亡相关基因的功能包括细胞因子产生、内肽酶活性、炎症调节和炎性小体复合物,并且细胞焦亡相关基因对胰腺腺癌微环境中的免疫细胞浸润有影响。
许多细胞焦亡相关的差异表达基因可能参与胰腺腺癌的发病机制,它们的高表达对生存有影响。GABARAP和IL18可能是胰腺腺癌有价值的研究靶点。