Literature DB >> 18499069

Correlation of genomic and expression alterations of AS3 with esophageal squamous cell carcinoma.

Yu Zhang1, Xiaoping Huang, Jun Qi, Cai Yan, Xin Xu, Yaling Han, Mingrong Wang.   

Abstract

Androgen-induced proliferation shutoff gene AS3, also known as APRIN, is a growth inhibitory gene that is initially implicated in prostate cancer. This gene is required for androgen-dependent growth arrest and is a primary target for 1,25(OH)(2)D(3) and androgens. Allelic loss at AS3 locus has been linked to a variety of cancers. However, the correlation of genomic and expression alterations of AS3 with esophageal squamous cell carcinoma (ESCC) is not well established. In this study, the genomic and expression alterations of AS3 in ESCC and their clinical significance are evaluated. Loss of heterozygosity (LOH) analysis using an AS3 intragenic microsatellite marker D13S171 revealed 72% allelic loss at AS3 locus in ESCC, which is significantly correlated with higher pathological grade (P=0.042). RT-PCR examination showed that AS3 mRNA obviously decreased in 44% tumors and its down-regulation was correlated with the sex of patients (P=0.03). Furthermore, the correlation between genomic and expression alterations of AS3 gene was analyzed in 18 ESCC specimens, which indicated that the consistency between allelic loss and decreased mRNA expression of AS3 was relatively poor. The results of this study indicate that the aberrant expression of AS3 may be involved in the tumorigenesis of esophagus and is responsible for the male predominance of ESCC.

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Year:  2008        PMID: 18499069     DOI: 10.1016/S1673-8527(08)60038-7

Source DB:  PubMed          Journal:  J Genet Genomics        ISSN: 1673-8527            Impact factor:   4.275


  5 in total

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Authors:  Min Sung Kim; Chang Hyeok An; Yeun Jun Chung; Nam Jin Yoo; Sug Hyung Lee
Journal:  Dig Dis Sci       Date:  2013-08-04       Impact factor: 3.199

2.  Overexpression of APRIN inhibits differentiation and proliferation and promotes apoptosis in P19 embryonal carcinoma cells.

Authors:  Xiang Zhou; Xiangqing Kong; Weiting Xu; Jianchang Chen
Journal:  Mol Biol Rep       Date:  2012-10-11       Impact factor: 2.316

3.  Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants.

Authors:  Joakim Klar; Helene Engstrand-Lilja; Khurram Maqbool; Jonas Mattisson; Lars Feuk; Niklas Dahl
Journal:  BMC Med Genomics       Date:  2020-06-26       Impact factor: 3.063

4.  Downregulation of APRIN expression increases cancer cell proliferation via an interleukin-6/STAT3/cyclin D axis.

Authors:  Min-Shik Sohn; Miae Kang; Seong-Man Kang; Sangwoo Bae
Journal:  Oncol Lett       Date:  2020-11-18       Impact factor: 2.967

5.  APRIN is a cell cycle specific BRCA2-interacting protein required for genome integrity and a predictor of outcome after chemotherapy in breast cancer.

Authors:  Rachel Brough; Ilirjana Bajrami; Radost Vatcheva; Rachael Natrajan; Jorge S Reis-Filho; Christopher J Lord; Alan Ashworth
Journal:  EMBO J       Date:  2012-01-31       Impact factor: 11.598

  5 in total

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