Department of Gastroenterology Surgery, The Central Hospital of Dalian University of Technology (Dalian Municipal Central Hospital), Dalian Shahekou District Southwest Road No. 826, Dalian, 116033, PR China.
Department of Graduate School, Dalian Medical University, Dalian, 116044, China.
BMC Gastroenterol. 2024 Sep 28;24(1):325. doi: 10.1186/s12876-024-03430-5.
The stromal cell derived factor 2 (SDF2) relates closely to the occurrence and development of several kind of cancers. There are few studies to investigate the clinicopathological and prognostic significance of SDF2 in gastric cancer (GC) patients.
We detected SDF2 expression in GC and normal gastric tissues using bioinformatics, western blot and immunohistochemistry. Furthermore, we tested the relationship between SDF2 expression and clinicopathological characteristics and prognosis of GC patients.
Bioinformatics, western blot and immunohistochemistry results showed that SDF2 expression in GC tissue was higher than that in normal gastric tissue (P < 0.01). SDF2 expression was associated with Borrmann classification III-IV (χ = 6.484, P = 0.011), depth of infiltration T-T (χ = 9.140, P = 0.003), positive lymph node metastasis (χ = 24.945, P = 0.000) and TNM III-IV stage (χ = 9.945, P = 0.002) of GC patients. The Cox regression analysis indicated that distant metastasis M1 stage (HR = 6.026, 95% CI: 1.880-19.318, P = 0.003), TNM III-IV (HR = 1.833, 95% CI: 1.023-3.287, P = 0.042) and SDF2 high expression (HR = 2.091, 95% CI: 1.064-4.108, P = 0.032) were independent risk factors for OS of GC patients. Kaplan-Meier test showed that the OS of GC patients with SDF2 high expression was much poorer than that of GC patients with SDF2 low-expression (χ = 22.925, P = 0.000).
SDF2 expression is high in GC tissue and is correlated with Borrmann classification III-IV, tumor infiltration depth, positive lymph node metastasis and TNM III-IV stage of GC patients. GC patients with SDF2 high-expression have significantly poor OS.
基质细胞衍生因子 2(SDF2)与多种癌症的发生和发展密切相关。目前关于 SDF2 在胃癌(GC)患者中的临床病理和预后意义的研究较少。
我们使用生物信息学、western blot 和免疫组织化学检测 GC 和正常胃组织中的 SDF2 表达。此外,我们检测了 SDF2 表达与 GC 患者临床病理特征和预后的关系。
生物信息学、western blot 和免疫组织化学结果表明,GC 组织中 SDF2 的表达高于正常胃组织(P<0.01)。SDF2 表达与 Borrmann 分类 III-IV(χ2=6.484,P=0.011)、浸润深度 T-T(χ2=9.140,P=0.003)、阳性淋巴结转移(χ2=24.945,P=0.000)和 TNM III-IV 期(χ2=9.945,P=0.002)有关。Cox 回归分析表明,远处转移 M1 期(HR=6.026,95%CI:1.880-19.318,P=0.003)、TNM III-IV 期(HR=1.833,95%CI:1.023-3.287,P=0.042)和 SDF2 高表达(HR=2.091,95%CI:1.064-4.108,P=0.032)是 GC 患者 OS 的独立危险因素。Kaplan-Meier 检验显示,SDF2 高表达的 GC 患者 OS 明显差于 SDF2 低表达的 GC 患者(χ2=22.925,P=0.000)。
GC 组织中 SDF2 表达较高,与 Borrmann 分类 III-IV、肿瘤浸润深度、阳性淋巴结转移和 GC 患者的 TNM III-IV 期相关。SDF2 高表达的 GC 患者 OS 明显较差。