Department of Pulmonary and Critical Care Medicine, Ningbo Medical Center Lihuili Hospital, 1111 Jiangnan Road, Zhejiang, 315000, China.
BMC Cancer. 2022 Jun 21;22(1):681. doi: 10.1186/s12885-022-09756-1.
The C-X-C chemokine receptor 4 (CXCR4) has been suggested to play an important role in several types of cancers and is related to biological behaviors connected with tumor progression. However, the clinical significance and application of CXCR4 in lung cancer remain disputable. Thus, we conducted a meta-analysis to investigate the impact of CXCR4 expression on survival and clinicopathological features in lung cancer.
Comprehensive literature searches were conducted in PubMed, Embase and Web of Science for relevant studies. We pooled hazard ratios (HRs)/odds ratios (ORs) with 95% confidence intervals (CIs) by STATA 12.0 to evaluate the potential value of CXCR4 expression.
Twenty-seven relevant articles involving 2932 patients with lung cancer were included in our meta-analysis. The results revealed that CXCR4 expression was apparently associated with poor overall survival (OS) (HR 1.61, 95% CI 1.42-1.82) and disease-free survival (HR 3.39, 95% CI 2.38-4.83). Furthermore, a significant correlation with poor OS was obvious in non-small cell lung cancer patients (HR 1.59, 95% CI 1.40-1.81) and in patients showing CXCR4 expression in the cytoplasm (HR 2.10, 95% CI 1.55-2.84) and the membrane (HR 1.74, 95% CI 1.24-2.45). CXCR4 expression was significantly associated with men (OR 1.32, 95% CI 1.08-1.61), advanced tumor stages (T3-T4) (OR 2.34, 95% CI 1.28-4.28), advanced nodal stages (N > 0) (OR 2.34, 95% CI 1.90-2.90), distant metastasis (OR 3.65, 95% CI 1.53-8.69), advanced TNM stages (TNM stages III, IV) (OR 3.10, 95% CI 1.95-4.93) and epidermal growth factor receptor (EGFR) expression (OR 2.44, 95% CI 1.44-4.12) but was not associated with age, smoking history, histopathology, differentiation, lymphatic vessel invasion or local recurrence.
High expression of CXCR4 is related to tumor progression and might be an adverse prognostic factor for lung cancer.
C-X-C 趋化因子受体 4(CXCR4)被认为在多种类型的癌症中发挥着重要作用,与肿瘤进展相关的生物学行为有关。然而,CXCR4 在肺癌中的临床意义和应用仍存在争议。因此,我们进行了一项荟萃分析,以研究 CXCR4 表达对肺癌患者生存和临床病理特征的影响。
我们在 PubMed、Embase 和 Web of Science 中进行了全面的文献检索,以寻找相关研究。我们使用 STATA 12.0 汇总了风险比(HRs)/优势比(ORs)及其 95%置信区间(CIs),以评估 CXCR4 表达的潜在价值。
我们的荟萃分析纳入了 27 项涉及 2932 例肺癌患者的相关研究。结果表明,CXCR4 表达与总生存期(OS)(HR 1.61,95%CI 1.42-1.82)和无病生存期(DFS)(HR 3.39,95%CI 2.38-4.83)明显相关。此外,在非小细胞肺癌患者中,与 OS 不良显著相关(HR 1.59,95%CI 1.40-1.81),在细胞质(HR 2.10,95%CI 1.55-2.84)和膜(HR 1.74,95%CI 1.24-2.45)中表达 CXCR4 的患者中,也有明显的相关性。CXCR4 表达与男性(OR 1.32,95%CI 1.08-1.61)、晚期肿瘤分期(T3-T4)(OR 2.34,95%CI 1.28-4.28)、晚期淋巴结分期(N>0)(OR 2.34,95%CI 1.90-2.90)、远处转移(OR 3.65,95%CI 1.53-8.69)、晚期 TNM 分期(TNM 分期 III、IV)(OR 3.10,95%CI 1.95-4.93)和表皮生长因子受体(EGFR)表达(OR 2.44,95%CI 1.44-4.12)显著相关,但与年龄、吸烟史、组织病理学、分化、淋巴管浸润或局部复发无关。
CXCR4 的高表达与肿瘤进展有关,可能是肺癌的不良预后因素。