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

被引:43
作者
Das, Sudipto
Hahn, Yoonsoo
Nagata, Satoshi
Willingham, Mark C.
Bera, Tapan K.
Lee, Byungkook
Pastan, Ira
机构
[1] NCI, Mol Biol Lab, Ctr Canc Res, NIH, Bethesda, MD 20892 USA
[2] Wake Forest Univ, Sch Med, Dept Pathol, Winston Salem, NC 27109 USA
关键词
D O I
10.1158/0008-5472.CAN-06-2673
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 similar to 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.
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收藏
页码:1594 / 1601
页数:8
相关论文
共 18 条
[1]   NGEP, a gene encoding a membrane protein detected only in prostate cancer and normal prostate [J].
Bera, TK ;
Das, S ;
Maeda, H ;
Beers, R ;
Wolfgang, CD ;
Kumar, V ;
Hahn, Y ;
Lee, BK ;
Pastan, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :3059-3064
[2]   POTE, a highly homologous gene family located on numerous chromosomes and expressed in prostate, ovary, testis, placenta, and prostate cancer [J].
Bera, TK ;
Zimonjic, DB ;
Popescu, NC ;
Sathyanarayana, BK ;
Kumar, V ;
Lee, B ;
Pastan, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (26) :16975-16980
[3]  
BERA TK, 2005, CANC DRUG DISC DEV, P31
[4]  
Carruba G, 2002, PROSTATE, V50, P73
[5]  
Carruba G, 2002, ANN NY ACAD SCI, V963, P156
[6]  
Galindo BE, 2005, INT J MOL MED, V16, P919
[7]   CHROMA: consensus-based colouring of multiple alignments for publication [J].
Goodstadt, L ;
Ponting, CP .
BIOINFORMATICS, 2001, 17 (09) :845-846
[8]   Alterations in gap junction protein expression in human benign prostatic hyperplasia and prostate cancer (vol 166, pg 2269, 2001) [J].
Habermann, H ;
Ray, V ;
Habermann, W ;
Prins, GS .
JOURNAL OF UROLOGY, 2002, 167 (02) :655-660
[9]   Cancer statistics, 2006 [J].
Jemal, A ;
Siegel, R ;
Ward, E ;
Murray, T ;
Xu, JQ ;
Smigal, C ;
Thun, MJ .
CA-A CANCER JOURNAL FOR CLINICIANS, 2006, 56 (02) :106-130
[10]   The human prostate cancer cell line LNCaP bears functional membrane testosterone receptors, which increase PSA secretion and modify actin cytoskeleton [J].
Kampa, M ;
Papakonstanti, EA ;
Hatzoglou, A ;
Stathopoulos, EN ;
Stournaras, C ;
Castanas, E .
FASEB JOURNAL, 2002, 16 (09) :1429-+