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High expression level of T-box transcription factor 5 predicts unfavorable survival in stage I and II gastric adenocarcinoma

The expression of T-box transcription factor 5 (TBX5) has previously been observed in human cancer. The aim of the present study was to investigate TBX5 expression and its potential clinical significance in gastric cancer (GC). Using reverse transcription-quantitative polymerase chain reaction, the...

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Detalles Bibliográficos
Autores principales: ZHENG, YAN, LI, YUAN-FANG, WANG, WEI, CHEN, YONG-MING, WANG, DAN-DAN, ZHAO, JING-JING, PAN, QIU-ZHONG, JIANG, SHAN-SHAN, ZHANG, XIAO-FEI, YUAN, SHU-QIANG, QIU, HAI-BO, HUANG, CHUN-YU, ZHAO, BAI-WEI, ZHOU, ZHI-WEI, XIA, JIAN-CHUAN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4579827/
https://www.ncbi.nlm.nih.gov/pubmed/26622790
http://dx.doi.org/10.3892/ol.2015.3515
Descripción
Sumario:The expression of T-box transcription factor 5 (TBX5) has previously been observed in human cancer. The aim of the present study was to investigate TBX5 expression and its potential clinical significance in gastric cancer (GC). Using reverse transcription-quantitative polymerase chain reaction, the TBX5 mRNA expression levels in 30 pairs of surgically resected healthy gastric tissues and early stage (stages I and II) GC tissues were evaluated. The TBX5 mRNA expression levels were increased in GC stage I and II tumor tissues (P=0.01, n=30) compared with the matched adjacent non-tumor tissue. However, no significant difference was observed in TBX5 mRNA expression levels in matched adjacent non-tumor tissue compared with the tumor tissue from stage III and IV GC samples (P=0.318, n=30). Immunohistochemical analysis for TBX5 expression was performed on 161 paraffin-embedded stage I and II GC tissue blocks. Statistical analysis was performed to evaluate the associations between TBX5 expression, clinicopathological factors and prognosis. Patients with stage I and II GC and tumors with high TBX5 expression levels presented poor overall survival (OS) rate (P=0.024). The Cox proportional hazards model analysis demonstrated that TBX5 expression was an independent risk factor (P=0.017). The present study indicates that high expression of TBX5 is associated with unfavorable OS rates in patients with stage I and II GC. In conclusion, the expression of TBX5 may be a valuable biomarker for the selection of cases of high-risk stage I and II GC.