Literature DB >> 17308099

NGEP, a prostate-specific plasma membrane protein that promotes the association of LNCaP cells.

Sudipto Das1, Yoonsoo Hahn, Satoshi Nagata, Mark C Willingham, Tapan K Bera, Byungkook Lee, Ira Pastan.   

Abstract

NGEP is a prostate-specific gene identified by analysis of expressed sequence tag databases. RNA analysis revealed two spliced forms of NGEP mRNA: a short form encoding a soluble protein (NGEP-S) and a long form encoding a polytopic membrane protein (NGEP-L). Transient expression of myc epitope-tagged NGEP-L showed that it was localized to the plasma membrane. We have now produced a specific antibody to the COOH terminus of NGEP-L and showed that it detects an approximately 100-kDa protein in extracts of normal prostate and prostate cancers that contain high levels of NGEP mRNA. The antibody detects a protein that is highly expressed on the apical and the lateral surfaces of normal prostate and prostate cancer cells by immunohistochemistry. The antibody does not detect a protein in the prostate cancer cell line LNCaP, which has very low NGEP mRNA levels. To study NGEP function, two stable LNCaP cell lines were prepared by transfection with NGEP-L and shown to contain similar amounts of NGEP-L protein as human prostate. Confocal immunofluorescence showed that NGEP-L is present on the plasma membrane of the transfected LNCaP cells and is highly concentrated at cell:cell contact regions. Furthermore, as the cell density increased, the cells formed large aggregates. A specific RNA interference that lowered NGEP-L levels prevented formation of cell aggregates. Our results suggest that NGEP-L has a role in promoting cell contact-dependent interactions of LNCaP prostate cancer cells and also that NGEP is a promising immunotherapy target for prostate cancer.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17308099     DOI: 10.1158/0008-5472.CAN-06-2673

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  23 in total

1.  ANOs 3-7 in the anoctamin/Tmem16 Cl- channel family are intracellular proteins.

Authors:  Charity Duran; Zhiqiang Qu; Adeboye O Osunkoya; Yuanyuan Cui; H Criss Hartzell
Journal:  Am J Physiol Cell Physiol       Date:  2011-11-09       Impact factor: 4.249

Review 2.  International Union of Basic and Clinical Pharmacology. LXXXV: calcium-activated chloride channels.

Authors:  Fen Huang; Xiuming Wong; Lily Y Jan
Journal:  Pharmacol Rev       Date:  2011-11-16       Impact factor: 25.468

3.  Identification of Novel Susceptibility Loci and Genes for Prostate Cancer Risk: A Transcriptome-Wide Association Study in Over 140,000 European Descendants.

Authors:  Lang Wu; Jifeng Wang; Qiuyin Cai; Taylor B Cavazos; Nima C Emami; Jirong Long; Xiao-Ou Shu; Yingchang Lu; Xingyi Guo; Joshua A Bauer; Bogdan Pasaniuc; Kathryn L Penney; Matthew L Freedman; Zsofia Kote-Jarai; John S Witte; Christopher A Haiman; Rosalind A Eeles; Wei Zheng
Journal:  Cancer Res       Date:  2019-05-17       Impact factor: 12.701

4.  Classification of Homo sapiens gene behavior using linear discriminant analysis fused with minimum entropy mapping.

Authors:  Joyshri Das; Soma Barman Mandal
Journal:  Med Biol Eng Comput       Date:  2021-02-17       Impact factor: 2.602

5.  Anoctamin and transmembrane channel-like proteins are evolutionarily related.

Authors:  Yoonsoo Hahn; Dong Seon Kim; Ira H Pastan; Byungkook Lee
Journal:  Int J Mol Med       Date:  2009-07       Impact factor: 4.101

6.  Topology of NGEP, a prostate-specific cell:cell junction protein widely expressed in many cancers of different grade level.

Authors:  Sudipto Das; Yoonsoo Hahn; Dawn A Walker; Satoshi Nagata; Mark C Willingham; Donna M Peehl; Tapan K Bera; Byungkook Lee; Ira Pastan
Journal:  Cancer Res       Date:  2008-08-01       Impact factor: 12.701

7.  Expression of genes encoding multi-transmembrane proteins in specific primate taste cell populations.

Authors:  Bryan D Moyer; Peter Hevezi; Na Gao; Min Lu; Dalia Kalabat; Hortensia Soto; Fernando Echeverri; Bianca Laita; Shaoyang Anthony Yeh; Mark Zoller; Albert Zlotnik
Journal:  PLoS One       Date:  2009-12-04       Impact factor: 3.240

8.  New gene expressed in prostate: a potential target for T cell-mediated prostate cancer immunotherapy.

Authors:  Vittore Cereda; Diane J Poole; Claudia Palena; Sudipto Das; Tapan K Bera; Cinzia Remondo; James L Gulley; Philip M Arlen; Junko Yokokawa; Ira Pastan; Jeffrey Schlom; Kwong Y Tsang
Journal:  Cancer Immunol Immunother       Date:  2009-06-04       Impact factor: 6.968

9.  Programmed cell death 4 (PDCD4) suppresses metastastic potential of human hepatocellular carcinoma cells.

Authors:  Shuhong Zhang; Jianfeng Li; Ying Jiang; Yijun Xu; Chengyong Qin
Journal:  J Exp Clin Cancer Res       Date:  2009-05-29

10.  Differential expression of apoptotic genes PDIA3 and MAP3K5 distinguishes between low- and high-risk prostate cancer.

Authors:  Nicole Chui Pressinotti; Helmut Klocker; Georg Schäfer; Van-Duc Luu; Markus Ruschhaupt; Ruprecht Kuner; Eberhard Steiner; Annemarie Poustka; Georg Bartsch; Holger Sültmann
Journal:  Mol Cancer       Date:  2009-12-27       Impact factor: 27.401

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.