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TP73-AS1 as a predictor of clinicopathological parameters and prognosis in human malignancies: a meta and bioinformatics analysis.
Chen, Caizhi; Wang, Jingjing; Feng, Yeqian; Liang, Ye; Huang, Yan; Zou, Wen.
Afiliación
  • Chen C; Department of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, China.
  • Wang J; Department of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, China.
  • Feng Y; Department of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, China.
  • Liang Y; Department of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, China.
  • Huang Y; Department of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, China.
  • Zou W; Department of Oncology, The Second Xiangya Hospital of Central South University, Changsha, 410000, Hunan, China. zouwen29w@csu.edu.cn.
BMC Cancer ; 22(1): 581, 2022 May 25.
Article en En | MEDLINE | ID: mdl-35614413
ABSTRACT

BACKGROUND:

Long non-coding RNA P73 antisense RNA 1 T (non-protein coding), also known as Lnc RNA TP73-AS1, is dysregulated in various tumors but the correlation between its expression and clinicopathological parameters and/or prognoses in cancer patients is inconclusive. Here, we performed a meta-analysis to evaluate the prognostic value of Lnc RNA TP73-AS1 for malignancies.

METHODS:

We systematically searched four online databases including PubMed, the Web of Science, Embase, and the Cochrane Library for eligible articles published up to June 29/2020. Odds ratios (ORs) and Pooled hazard ratios (HRs) with 95% confidence intervals (95% CIs) were used to assess the association of TP73-AS1 expression with prognostic and clinicopathological parameters. We further validated TP73-AS1 expression in various malignancies and its potential prognostic value using the GEPIA online database. We predicted potential biological processes and relevant signal mechanisms through the public databases.

RESULTS:

A total of 26 studies examining 14 cancers were analyzed to evaluate the relationship between TP73-AS1 expression, clinicopathological features and prognostic indicators. The results indicated that TP73-AS1 expression markedly correlates with TNM stage (OR = 3.27,95% CI2.43-4.39, P < 0.00001), tumor size (OR = 3.00, 95%CI2.08-4.35, P < 0.00001), lymph node metastasis (OR = 2.77, 95%CI1.42-5.38,P < 0.00001) and distant metastasis (OR = 4.50,95%CI2. 62-7.73,P < 0.00001). No correlation with age (OR = 1.12,95%CI0.77-1.64, P > 0.05), gender (OR = 1.08, 95%CI0.84-1.38, P > 0.05) or differentiation (OR = 1.39, 95%CI0.71-2.70, P = 0.340) was observed. TP73-AS1 overexpression was a biomarker of poor Overall survival(OS)(HR = 1.85,95%CI1.53-2.22, P < 0.00001) and Disease-Free-Survival (DFS) (HR = 1.57,95%CI1.03-2.42, P < 0.05). Dysregulated TP73-AS1 expression and its prognostic value in various cancers was validated based on The Cancer Genome Atlas (TCGA). Further biological function predictions indicated that TP73-AS1 was involved in pro-oncogenic signaling.

CONCLUSIONS:

The upregulation of Lnc RNA TP73-AS1 was related to detrimental clinicopathological parameters and can be considered an indicator of poor prognosis for cancer malignancies.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: ARN Largo no Codificante / Neoplasias Tipo de estudio: Prognostic_studies / Risk_factors_studies / Systematic_reviews Idioma: En Revista: BMC Cancer Asunto de la revista: NEOPLASIAS Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: ARN Largo no Codificante / Neoplasias Tipo de estudio: Prognostic_studies / Risk_factors_studies / Systematic_reviews Idioma: En Revista: BMC Cancer Asunto de la revista: NEOPLASIAS Año: 2022 Tipo del documento: Article