» Articles » PMID: 21954337

Low Expression of TBX4 Predicts Poor Prognosis in Patients with Stage II Pancreatic Ductal Adenocarcinoma

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2011 Sep 29
PMID 21954337
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

This study was designed to investigate the expression of the T-box transcription factor 4 (TBX4), a tumor biomarker that was previously identified by proteomics, in pancreatic ductal adenocarcinoma (PDAC) and evaluate its clinical utility as a potential prognostic biomarkers for PDAC. The expression of TBX4 was detected in 77 stage II PDAC tumors by immunohistochemistry, and the results were analyzed with regard to clinicopathological characteristics and overall survival. Moreover, Tbx4 promoter methylation status in primary PDAC tumors and normal adjacent pancreas tissues was measured by bisulfite sequencing. Among 77 stage II PDAC tumors, 48 cases (62.3%) expressed TBX4 at a high level. No significant correlation between TBX4 expression and other clinicopathological parameters, except tumor grade and liver metastasis recurrence, was found. The survival of patients with TBX4-high expression was significantly longer than those with TBX4-low expression (P = 0.010). In multivariate analysis, low TBX4 expression was an independent prognostic factor for overall survival in patients with stage II PDAC. TBX4 promoter methylation status was frequently observed in both PDAC and normal adjacent pancreas. We conclude that a low level of TBX4 expression suggests a worse prognosis for patients with stage II PDAC. Down-regulation of the TBX4 gene in pancreas is less likely to be regulated by DNA methylation.

Citing Articles

Multiomics2Targets identifies targets from cancer cohorts profiled with transcriptomics, proteomics, and phosphoproteomics.

Deng E, Marino G, Clarke D, Diamant I, Resnick A, Ma W Cell Rep Methods. 2024; 4(8):100839.

PMID: 39127042 PMC: 11384097. DOI: 10.1016/j.crmeth.2024.100839.


Understanding the Conundrum of Pancreatic Cancer in the Omics Sciences Era.

Nicoletti A, Paratore M, Vitale F, Negri M, Quero G, Esposto G Int J Mol Sci. 2024; 25(14).

PMID: 39062863 PMC: 11276793. DOI: 10.3390/ijms25147623.


Context-dependent T-BOX transcription factor family: from biology to targeted therapy.

Li S, Luo X, Sun M, Wang Y, Zhang Z, Jiang J Cell Commun Signal. 2024; 22(1):350.

PMID: 38965548 PMC: 11225425. DOI: 10.1186/s12964-024-01719-2.


Expression and prognosis analysis of TBX2 subfamily in human lung carcinoma.

Mi R, Wang Q, Liu Q, Jiang F, Ji Y Discov Oncol. 2024; 15(1):51.

PMID: 38413457 PMC: 10899548. DOI: 10.1007/s12672-024-00900-w.


DNA Methylation Biomarkers as Prediction Tools for Therapeutic Response and Prognosis in Intermediate-Stage Hepatocellular Carcinoma.

Lu C, Hsiao C, Peng P, Huang S, Chuang M, Su H Cancers (Basel). 2023; 15(18).

PMID: 37760434 PMC: 10527266. DOI: 10.3390/cancers15184465.


References
1.
Rodriguez M, Aladowicz E, Lanfrancone L, Goding C . Tbx3 represses E-cadherin expression and enhances melanoma invasiveness. Cancer Res. 2008; 68(19):7872-81. DOI: 10.1158/0008-5472.CAN-08-0301. View

2.
Naiche L, Papaioannou V . Loss of Tbx4 blocks hindlimb development and affects vascularization and fusion of the allantois. Development. 2003; 130(12):2681-93. DOI: 10.1242/dev.00504. View

3.
Raimondi S, Maisonneuve P, Lowenfels A . Epidemiology of pancreatic cancer: an overview. Nat Rev Gastroenterol Hepatol. 2009; 6(12):699-708. DOI: 10.1038/nrgastro.2009.177. View

4.
Hasson P, DeLaurier A, Bennett M, Grigorieva E, Naiche L, Papaioannou V . Tbx4 and tbx5 acting in connective tissue are required for limb muscle and tendon patterning. Dev Cell. 2010; 18(1):148-56. PMC: 3034643. DOI: 10.1016/j.devcel.2009.11.013. View

5.
Agulnik S, Garvey N, Hancock S, Ruvinsky I, CHAPMAN D, Agulnik I . Evolution of mouse T-box genes by tandem duplication and cluster dispersion. Genetics. 1996; 144(1):249-54. PMC: 1207498. DOI: 10.1093/genetics/144.1.249. View