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血清 CXCL5 水平与阴茎癌的肿瘤进展有关。

Serum CXCL5 level is associated with tumor progression in penile cancer.

机构信息

Department of Urology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, P.R. China.

出版信息

Biosci Rep. 2021 Jan 29;41(1). doi: 10.1042/BSR20202133.

Abstract

Chemokine (C-X-C motif) ligand 5 is an important regulator of tumor progression in many cancers, and could serve as potential serum cancer biomarker. Our initial analysis identified CXCL5 as a cancer-related gene highly expressed in PC. Patients with PC exhibited markedly higher preoperative serum CXCL5 levels compared with that in healthy individuals (P<0.001). The area under the curve (AUC) was 0.880 with the sensitivity of 84.0%, and specificity of 80.4% to distinguish PC. Serum CXCL5 levels were also significantly decreased following tumor resection in patients with PC (P=0.001). Preoperative serum CXCL5 level was significantly associated with clinicopathological characteristics including T stage (P=0.001), nodal status (P<0.001), and pelvic lymph node metastasis (P=0.018). Cox regression analysis showed that serum CXCL5 level could serve as an independent prognostic factor for disease-free survival with a HR of 6.363 (95% CI: 2.185-18.531, P=0.001). CXCL5 and its receptor CXCR2 exhibited correlated expression pattern in PC tissues. Differential CXCL5 expression was observed in normal penile tissues, PC cell lines, and their culture supernatants. Furthermore, knockdown of CXCL5 or CXCR2 expression markedly suppressed malignant phenotypes (cell proliferation, clonogenesis, apoptosis escape, migration, and invasion), attenuated STAT3 and AKT signaling, and reduced MMP2/9 secretion in PC cell lines. In conclusion, our findings revealed that serum CXCL5 level might serve as a potential diagnostic and prognostic cancer biomarker for penile cancer. Autocrine CXCL5/CXCR2 signaling might activate multiple downstream oncogenic signaling pathways (STAT3, AKT, MMP2/9) to promote malignant progression of PC, which may warrant further investigation in the future.

摘要

趋化因子(C-X-C 基序)配体 5 是许多癌症中肿瘤进展的重要调节剂,可作为潜在的血清癌生物标志物。我们的初步分析表明,CXCL5 是 PC 中高度表达的癌相关基因。与健康个体相比,PC 患者术前血清 CXCL5 水平明显升高(P<0.001)。曲线下面积(AUC)为 0.880,灵敏度为 84.0%,特异性为 80.4%,可区分 PC。PC 患者肿瘤切除后血清 CXCL5 水平也明显降低(P=0.001)。术前血清 CXCL5 水平与包括 T 分期(P=0.001)、淋巴结状态(P<0.001)和盆腔淋巴结转移(P=0.018)在内的临床病理特征显著相关。Cox 回归分析表明,血清 CXCL5 水平可作为无病生存率的独立预后因素,风险比(HR)为 6.363(95%CI:2.185-18.531,P=0.001)。CXCL5 及其受体 CXCR2 在 PC 组织中表现出相关的表达模式。在正常阴茎组织、PC 细胞系及其培养上清液中观察到 CXCL5 的差异表达。此外,下调 CXCL5 或 CXCR2 的表达显著抑制了 PC 细胞系的恶性表型(细胞增殖、克隆形成、凋亡逃逸、迁移和侵袭),减弱了 STAT3 和 AKT 信号,并减少了 MMP2/9 的分泌。总之,我们的研究结果表明,血清 CXCL5 水平可能是阴茎癌潜在的诊断和预后生物标志物。自分泌 CXCL5/CXCR2 信号可能激活多个下游致癌信号通路(STAT3、AKT、MMP2/9),促进 PC 的恶性进展,这可能值得未来进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8113/7843497/efd2610124cb/bsr-41-bsr20202133-g1.jpg

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