Literature DB >> 11141474

Identification of a novel gene with increasing rate of suppression in high grade prostate cancers.

Y P Yu1, F Lin, M Bisceglia, D Krill, R Dhir, M Becich, J H Luo.   

Abstract

Prostate cancer is the second leading cause of cancer-related deaths in the United States. However, the underlying molecular events for prostate cancer development are not clear. In this study, we applied the recently developed technology known as differential subtraction chain (DSC) to identify a novel gene whose expression is inactivated in high grade prostate cancer. This gene, designated as SAPC, is expressed in normal prostate acinar cells. Its expression is dramatically down-regulated in high grade prostate cancers (4/4) but is unaltered in low grade prostate cancers. It encodes a 7.7-kd protein. Its sequence shares some homology with the cysteine-rich domain of 2-5A-dependent RNase L, which is a critical component of the interferon-induced apoptosis cascade. The selective inactivation in the more aggressive prostate cancers holds promise for SAPC as a potential prognostic marker for high grade prostate cancer.

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Year:  2001        PMID: 11141474      PMCID: PMC1850281          DOI: 10.1016/S0002-9440(10)63939-9

Source DB:  PubMed          Journal:  Am J Pathol        ISSN: 0002-9440            Impact factor:   4.307


  13 in total

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Journal:  Nucleic Acids Res       Date:  1999-10-01       Impact factor: 16.971

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  2 in total

1.  Myopodin, a synaptopodin homologue, is frequently deleted in invasive prostate cancers.

Authors:  F Lin; Y P Yu; J Woods; K Cieply; B Gooding; P Finkelstein; R Dhir; D Krill; M J Becich; G Michalopoulos; S Finkelstein; J H Luo
Journal:  Am J Pathol       Date:  2001-11       Impact factor: 4.307

2.  Dual modulation of Ras-Mnk and PI3K-AKT-mTOR pathways: A Novel c-FLIP inhibitory mechanism of 3-AWA mediated translational attenuation through dephosphorylation of eIF4E.

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Journal:  Sci Rep       Date:  2016-01-05       Impact factor: 4.379

  2 in total

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