Sun Xiaoyu, Jiang Haiyang, Huang Yufei, Xia Jing, Gu Jie, Sui Xinbing, Sun Xueni, Zhou Yucheng
School of Pharmacy, Hangzhou Normal University, Hangzhou, Zhejiang, China.
Department of Gastrointestinal & Pancreatic Surgery, Key Laboratory of Gastroenterology of Zhejiang Province, Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang, China.
PeerJ. 2025 May 30;13:e19517. doi: 10.7717/peerj.19517. eCollection 2025.
Pancreatic cancer is highly aggressive with limited treatment options. PLA2G16 has been implicated in cancer progression, but its role in prognosis and gemcitabine sensitivity in pancreatic cancer remains poorly understood.
Using TCGA data, the study assessed the correlation between PLA2G16 expression and patient survival. The expression of PLA2G16 in gemcitabine-resistant sensitive pancreatic cancer cells was also compared. siRNA-mediated knockdown of PLA2G16 was performed in drug-resistant PANC-1 cells to evaluate its impact on gemcitabine sensitivity. The relationship between PLA2G16 expression, immune infiltration, and molecular pathways in pancreatic cancer was explored using CIBERSORT and DAVID tools.
PLA2G16 was significantly overexpressed in pancreatic cancer tissues and associated with poorer patient survival. In PANC-1 cells, increased PLA2G16 expression correlated with gemcitabine resistance, and its knockdown improved drug sensitivity. PLA2G16 expression was linked to specific immune infiltration patterns and cancer-related molecular pathways.
Elevated PLA2G16 expression is associated with poor survival and gemcitabine resistance in pancreatic cancer, making it a potential prognostic marker and therapeutic target.
胰腺癌侵袭性强,治疗选择有限。磷脂酶A2G16(PLA2G16)与癌症进展有关,但其在胰腺癌预后和吉西他滨敏感性中的作用仍知之甚少。
利用癌症基因组图谱(TCGA)数据,该研究评估了PLA2G16表达与患者生存率之间的相关性。还比较了PLA2G16在吉西他滨耐药和敏感的胰腺癌细胞中的表达。在耐药的PANC-1细胞中进行小干扰RNA(siRNA)介导的PLA2G16敲低,以评估其对吉西他滨敏感性的影响。使用CIBERSORT和DAVID工具探讨PLA2G16表达、免疫浸润和胰腺癌分子通路之间的关系。
PLA2G16在胰腺癌组织中显著过表达,且与患者较差的生存率相关。在PANC-1细胞中,PLA2G16表达增加与吉西他滨耐药相关,敲低PLA2G16可提高药物敏感性。PLA2G16表达与特定的免疫浸润模式和癌症相关分子通路有关。
PLA2G16表达升高与胰腺癌患者的低生存率和吉西他滨耐药相关,使其成为一个潜在的预后标志物和治疗靶点。