Department of Gastrointestinal Surgery, Xiangya Hospital of Central South University, Changsha, 410000, China.
Department of The Hunan Provincial Key Lab of Precision Diagnosis and Treatment for Gastrointestinal Tumor, Xiangya Hospital of Central South University, Changsha, 410000, China.
Curr Pharm Biotechnol. 2022;23(7):946-958. doi: 10.2174/1389201022666210810100607.
The long non-coding RNA SNHG7 is upregulated in many types of cancer and plays a role as an oncogene. However, its overall predictive ability in human cancer prognosis has not been assessed using existing databases. Therefore, further study of its prognostic value and clinical significance in human malignancies is warranted.
We systematically collected relevant literature from multiple electronic document databases about the relationship between SNHG7 expression level and prognosis in patients with solid cancers. We further screenped them for eligibility. Pooled hazard ratios (HRs) with 95% confidence intervals (CIs) were used to assess the prognostic value. Odds ratios (ORs) and their 95% CIs were collected to evaluate the relationship between the expression of SNHG7 and clinicopathological features, including lymph node metastasis (LNM), tumour size, tumour node metastasis (TNM) stage and histological grade.
Fourteen original studies involving 971 patients were enrolled strictly following the inclusion and exclusion criteria. The meta-analysis showed that SNHG7 expression significantly correlated with poor overall survival (HR = 1.93, 95% CI: 1.64-2.26, p<0.001) in human cancer patients. In addition, the pooled OR indicated that overexpression of SNHG7 was associated with earlier LNM (OR = 1.83, 95% CI: 1.44-2.32; P <0.001), and advanced TNM stage (OR = 1.82, 95% CI: 1.44-2.30; P <0.001). Meanwhile, there was no significant heterogeneity between the selected studies, proving the reliability of the meta-analysis results.
High SNHG7 expression may predict poor oncological outcomes in patients with multiple human cancers, which could be a novel prognostic biomarker of unfulfilled clinicopathological features. However, further high-quality studies are needed to verify and strengthen the clinical value of SNHG7 in different types of cancer.
长链非编码 RNA SNHG7 在多种癌症中上调,发挥癌基因作用。然而,利用现有数据库尚未评估其在人类癌症预后中的整体预测能力。因此,进一步研究其在人类恶性肿瘤中的预后价值和临床意义是必要的。
我们系统地从多个电子文献数据库中收集了有关 SNHG7 表达水平与实体瘤患者预后关系的相关文献,并进一步筛选了符合条件的文献。使用合并风险比(HR)及其 95%置信区间(CI)来评估预后价值。收集比值比(OR)及其 95%CI 来评估 SNHG7 表达与临床病理特征(包括淋巴结转移、肿瘤大小、肿瘤淋巴结转移分期和组织学分级)之间的关系。
严格按照纳入和排除标准,共有 14 项原始研究,共纳入 971 例患者。meta 分析显示,SNHG7 表达与人类癌症患者的总体生存不良显著相关(HR=1.93,95%CI:1.64-2.26,p<0.001)。此外,汇总 OR 表明 SNHG7 过表达与较早的 LNM(OR=1.83,95%CI:1.44-2.32;P<0.001)和较晚的 TNM 分期(OR=1.82,95%CI:1.44-2.30;P<0.001)相关。同时,所选研究之间没有显著的异质性,证明了 meta 分析结果的可靠性。
SNHG7 高表达可能预示着多种人类癌症患者的不良肿瘤结局,它可能成为一种新的未满足的临床病理特征的预后生物标志物。然而,需要进一步的高质量研究来验证和加强 SNHG7 在不同类型癌症中的临床价值。