Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fudan University, Room 358, Building West 7, 130 Dongan Rd, Shanghai, 200032, China.
Department of General Surgery, Zhongshan Hospital, Fudan University, Room 1004, Building No.1, 180 Fenglin Rd, Shanghai, 200032, China.
Cancer Immunol Immunother. 2018 Feb;67(2):261-269. doi: 10.1007/s00262-017-2083-y. Epub 2017 Oct 31.
Chemokine (C-X-C motif) ligand 13 (CXCL13/BLC/BCA-1) is a cytokine from C-X-C chemokine family, which is selectively chemotactic for B cells. Previous research has demonstrated that high CXCL13 expression is correlated to poor prognosis in various cancers. However, the association between CXCL13 expression and gastric cancer is still unclear.
Intratumoral CXCL13 expression was evaluated by immunohistochemistry using a semi-quantitative method (modified H-score) in a testing set of 214 and a validation set of 227 randomly selected gastric cancer patients resected in 2008 in one institution. The median value was used as the cut-off point. We performed correlative analysis of CXCL-13 expression with clinicopathological variables, Kaplan-Meier analysis for association with overall survival (OS), and multivariate modeling.
High CXCL13 expression was associated with larger tumor diameter and shorter OS. By multivariate analysis, CXCL13 expression was associated with OS independently from clinicopathological factors. Within the T2-4 stage patients group, low CXCL13 expression was associated with longer survival, especially in the subgroup of patients (57.6%) who received adjuvant chemotherapy.
Intratumoral CXCL13 expression appears as an independent prognostic marker for patients after gastric cancer resection. In addition, CXCL13 expression may serve as a predictive biomarker of response to postoperative adjuvant chemotherapy in these patients.
趋化因子(C-X-C 基序)配体 13(CXCL13/BLC/BCA-1)是 C-X-C 趋化因子家族的细胞因子,对 B 细胞具有选择性趋化作用。先前的研究表明,高 CXCL13 表达与多种癌症的不良预后相关。然而,CXCL13 表达与胃癌之间的关联尚不清楚。
采用免疫组织化学半定量方法(改良 H 评分),在一个机构于 2008 年随机选择的 214 例检测集和 227 例验证集中评估肿瘤内 CXCL13 表达。使用中位数作为截断值。我们对 CXCL-13 表达与临床病理变量进行了相关性分析,对总生存期(OS)进行了 Kaplan-Meier 分析,并进行了多变量建模。
高 CXCL13 表达与肿瘤直径较大和 OS 较短有关。通过多变量分析,CXCL13 表达与 OS 独立于临床病理因素相关。在 T2-4 期患者组中,低 CXCL13 表达与生存时间延长相关,尤其是在接受辅助化疗的患者亚组(57.6%)中。
肿瘤内 CXCL13 表达似乎是胃癌切除术后患者的独立预后标志物。此外,CXCL13 表达可能是这些患者术后辅助化疗反应的预测生物标志物。