Yu Pengcheng, He Weiyang, Zhang Yanqiang, Hu Can, Wu Yue, Wang Yi, Bao Zhehan, Xia Yuhang, Zhang Ruolan, Cao Mengxuan, Yuan Li, Cheng Xiangdong, Xu Zhiyuan
First Clinical Medical College of Zhejiang Chinese Medical University, Hangzhou 310053, China.
Department of Gastrointestinal Surgery, Sichuan Cancer Hospital, Chengdu 610042, China.
J Oncol. 2022 Jul 5;2022:8829649. doi: 10.1155/2022/8829649. eCollection 2022.
Secreted frizzled-related protein 4 (SFRP4) is a member of the SFRP family, which functions as either a tumor suppressor or a prooncogenic factor in distinct tumor types. Our research aimed to explore the expression of SFRP4 in gastric cancer, its prognostic significance, and its relationship with immune cell infiltration.
Gastric cancer and paracancerous tissue specimens from surgically resected gastric cancer patients were collected to construct tissue microarrays, and immunohistochemistry was used to detect the expression of SFRP4, PD-L1, CD3 , CD4 , and CD8 in these microarrays. The differential expression of SFRP4 and its relationship with the immune microenvironment were evaluated using the TIMER and TISIDB databases. Finally, patient survival was assessed.
SFRP4 expression was elevated in gastric cancer tissues and linked to a poor prognosis (=0.021). The 5-year survival rate for patients with high SFRP4 expression was only 39.81% but reached 60.02% for patients with low SFRP4 expression. Increased SFRP4 expression correlated with high CD8 T-cell infiltration (=0.015) and positive PD-L1 expression (=0.036). High SFRP4 expression was an independent predictor of overall survival (=0.024 in univariable analysis, =0.011 in multivariable analysis). Using online databases, we found that SFRP4 expression was higher in gastric cancer tissues and substantially was associated with the immune microenvironment.
SFRP4 is an oncogenic driver that can predict patient survival time in gastric cancer, as well as an important immune-related factor. SFRP4 may be important for guiding immunotherapy in gastric cancer patients.
分泌型卷曲相关蛋白4(SFRP4)是SFRP家族的一员,在不同肿瘤类型中既作为肿瘤抑制因子发挥作用,也作为促癌因子发挥作用。我们的研究旨在探讨SFRP4在胃癌中的表达、其预后意义以及与免疫细胞浸润的关系。
收集手术切除的胃癌患者的胃癌组织和癌旁组织标本,构建组织芯片,采用免疫组织化学方法检测这些芯片中SFRP4、PD-L1、CD3、CD4和CD8的表达。利用TIMER和TISIDB数据库评估SFRP4的差异表达及其与免疫微环境的关系。最后,评估患者的生存率。
SFRP4在胃癌组织中的表达升高,且与预后不良相关(P=0.021)。SFRP4高表达患者的5年生存率仅为39.81%,而SFRP4低表达患者的5年生存率达到60.02%。SFRP4表达增加与CD8+T细胞浸润增加(P=0.015)和PD-L1阳性表达(P=0.036)相关。SFRP4高表达是总生存的独立预测因子(单因素分析P=0.024,多因素分析P=0.011)。通过在线数据库,我们发现SFRP4在胃癌组织中的表达较高,且与免疫微环境密切相关。
SFRP4是一种致癌驱动因子,可预测胃癌患者的生存时间,也是一个重要的免疫相关因子。SFRP4可能对指导胃癌患者的免疫治疗具有重要意义。