Clinicopathological and prognostic significance of LINC00673 in human malignancy: a review and meta-analysis

Biosci Rep. 2021 Jul 30;41(7):BSR20211175. doi: 10.1042/BSR20211175.

Abstract

Background: We conducted this research to investigate the relationship between long intergenic non-protein coding RNA 673 (linc00673) expression and prognosis and clinicopathological parameters in human malignancies.

Methods: The PubMed, Embase, WOS, and CNKI databases were used to collect eligible research data before 4 January 2021. Meta-analysis was performed using Stata 12.0 software. Pooled odds ratios (ORs) or hazard ratios (HRs) and their 95% confidence interval (CIs) were calculated to evaluate the association of linc00673 expression with survival outcomes and clinical parameters.

Results: We finally included 17 articles and a total of 1539 cases for the meta-analysis. The results indicated that linc00673 was significantly correlated with T stage (P=0.006), tumor stage (P<0.001), lymph node metastasis (P<0.001), and distant metastasis (P<0.001). In addition, the results suggested that elevated linc00673 expression predicted a poor overall survival (OS) time (P=0.013) and acted as an independent prognostic factor (P<0.001) for OS in patients with malignancy. Although potential evidence of publication bias was found in the studies on OS in relation to tumor stage in the multivariate analysis, the trim-and-fill analysis confirmed that the results remained stable.

Conclusions: Overexpression of linc00673 was significantly correlated with shorter OS time in patients with malignant tumors. Moreover, the increased expression level of linc00673 was significantly correlated with T stage, tumor stage, lymph node metastasis, and distant metastasis. The results presented in this article revealed that linc00673 might be involved in the progression and invasion of malignancy and serve as a novel prognostic biomarker and potential therapeutic target for malignancy.

Keywords: Linc00673; malignant tumour; meta-analysis; prognosis.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Biomarkers, Tumor / genetics*
  • Female
  • Humans
  • Lymphatic Metastasis
  • Male
  • Neoplasm Staging
  • Neoplasms / genetics*
  • Neoplasms / mortality
  • Neoplasms / pathology
  • Neoplasms / therapy
  • Predictive Value of Tests
  • RNA, Long Noncoding / genetics*
  • Risk Assessment
  • Risk Factors

Substances

  • Biomarkers, Tumor
  • RNA, Long Noncoding
  • long non-coding RNA SLNCR1, human