Literature DB >> 23020249

Upregulated ataxia-telangiectasia group D complementing gene correlates with poor prognosis in patients with esophageal squamous cell carcinoma.

W Lai1, J Zhao, C Zhang, D Cui, J Lin, Y He, H Zheng, X Wu, M Yang.   

Abstract

The ataxia-telangiectasia group D complementing gene (ATDC) plays significant roles in various human cancers. However, the clinical significance of ATDC in esophageal squamous cell carcinoma (ESCC) has not been investigated. The ATDC messenger RNA level of 40 paired ESCC and nonneoplastic tissues were evaluated using quantitative real-time polymerase chain reaction, 10 pairs of which were also used for Western blot analysis. In addition, immunohistochemical staining was performed to detect the ATDC expression in 118 paraffin-embedded cancerous and matched nonneoplastic tissues, and the correlation of ATDC expression with the clinicopathological parameters and prognosis of the ESCC patients was analyzed. The quantitative real-time polymerase chain reaction, immunohistochemical staining, and Western blot results demonstrated that the expression level of ATDC was significantly higher in ESCC tissue than in matched noncancerous tissues. Both ATDC messenger RNA and protein expression in the ESCC tissue were significantly correlated with tumor differentiation, stage, and lymph node metastasis. However, there was no significant difference in ATDC expression based on patient age or gender. Moreover, the results of both univariate and multivariate analyses showed that increased ATDC expression was correlated with a shorter 5-year survival time for ESCC patients after surgery. We concluded that increased ATDC expression is associated with poor clinical outcomes and that this marker might be a useful indicator for prognosis and a promising target for therapy in ESCC patients.
© 2012 Copyright the Authors. Journal compilation © 2012, Wiley Periodicals, Inc. and the International Society for Diseases of the Esophagus.

Entities:  

Keywords:  ATDC; ESCC; IHC; prognosis

Mesh:

Substances:

Year:  2012        PMID: 23020249     DOI: 10.1111/j.1442-2050.2012.01400.x

Source DB:  PubMed          Journal:  Dis Esophagus        ISSN: 1120-8694            Impact factor:   3.429


  8 in total

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Journal:  J Biol Chem       Date:  2015-09-17       Impact factor: 5.157

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Journal:  Thorac Cancer       Date:  2015-01-07       Impact factor: 3.500

3.  ATDC is required for the initiation of KRAS-induced pancreatic tumorigenesis.

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Journal:  Genes Dev       Date:  2019-05-02       Impact factor: 11.361

Review 4.  The Tripartite Nexus: Autophagy, Cancer, and Tripartite Motif-Containing Protein Family Members.

Authors:  Michael A Mandell; Bhaskar Saha; Todd A Thompson
Journal:  Front Pharmacol       Date:  2020-03-11       Impact factor: 5.810

Review 5.  TRIM29 in Cutaneous Squamous Cell Carcinoma.

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Journal:  Front Med (Lausanne)       Date:  2021-12-20

6.  TRIM29 as a prognostic predictor for multiple human malignant neoplasms: a systematic review and meta-analysis.

Authors:  Chao Liang; Huiyu Dong; Chenkui Miao; Jundong Zhu; Jie Wang; Pu Li; Jie Li; Zengjun Wang
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7.  ATDC mediates a TP63-regulated basal cancer invasive program.

Authors:  Phillip L Palmbos; Yin Wang; Armand Bankhead Iii; Alan J Kelleher; Lidong Wang; Huibin Yang; McKenzie L Ahmet; Erica R Gumkowski; Samuel D Welling; Brian Magnuson; Jacob Leflein; Guadalupe Lorenzatti Hiles; Ethan V Abel; Michele L Dziubinski; Sumithra Urs; Mark L Day; Mats E Ljungman; Diane M Simeone
Journal:  Oncogene       Date:  2019-01-14       Impact factor: 9.867

8.  Identification of a Novel Oncogenic Fusion Gene SPON1-TRIM29 in Clinical Ovarian Cancer That Promotes Cell and Tumor Growth and Enhances Chemoresistance in A2780 Cells.

Authors:  Saya Nagasawa; Kazuhiro Ikeda; Daisuke Shintani; Chiujung Yang; Satoru Takeda; Kosei Hasegawa; Kuniko Horie; Satoshi Inoue
Journal:  Int J Mol Sci       Date:  2022-01-08       Impact factor: 5.923

  8 in total

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