Literature DB >> 15761874

D-TMPP: a novel androgen-regulated gene preferentially expressed in prostate and prostate cancer that is the first characterized member of an eukaryotic gene family.

Andrea Kiessling1, Bernd Weigle, Susanne Fuessel, Reinhard Ebner, Axel Meye, Michael A Rieger, Marc Schmitz, Achim Temme, Michael Bachmann, Manfred P Wirth, E Peter Rieber.   

Abstract

BACKGROUND: The understanding of the molecular biology of the prostate and the process of prostate carcinogenesis is brought forward by the identification and characterization of new genes specifically expressed in prostate tissue. The encoded proteins may, in addition, provide novel diagnostic and therapeutic tools in prostate carcinoma (PCa). Here, we identify the novel gene Dresden-transmembrane protein of the prostate (D-TMPP) that is overexpressed in human prostate and prostate cancer.
METHODS: Proceeding from a prostate-specific expressed sequence tag identified with an Affymetrix chip-based expression database, the full-length cDNA of the novel gene was isolated from prostate tissue. The potential protein-coding function of the open reading frame (ORF) was tested by in vitro transcription-coupled translation and recombinant expression in transfected prostate cancer cells. The expression pattern of D-TMPP in malignant and nonmalignant tissues and tumor cell lines was analyzed by hybridization of a radioactively labeled cDNA probe with a multiple tissue expression array and by a quantitative real-time PCR assay.
RESULTS: The D-TMPP-mRNA encodes a putative seven-span transmembrane protein of 883 amino acids and is selectively overexpressed in prostate tissue. D-TMPP represents the first cloned and characterized transcript of a family of eukaryotic genes. D-TMPP transcripts were detected in all analyzed pairs (n = 25) of malignant and nonmalignant prostate tissues. In the androgen-dependent PCa cell line LNCaP, D-TMPP was upregulated by methyltrienolone.
CONCLUSIONS: We describe the novel prostate-restricted molecule D-TMPP widely expressed in prostate cancer tissues. Copyright 2005 Wiley-Liss, Inc.

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Year:  2005        PMID: 15761874     DOI: 10.1002/pros.20250

Source DB:  PubMed          Journal:  Prostate        ISSN: 0270-4137            Impact factor:   4.104


  7 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

2.  Genome-wide linkage scan for prostate cancer susceptibility in Finland: evidence for a novel locus on 2q37.3 and confirmation of signal on 17q21-q22.

Authors:  Cheryl D Cropp; Claire L Simpson; Tiina Wahlfors; Nati Ha; Asha George; MaryPat S Jones; Ursula Harper; Damaris Ponciano-Jackson; Tiffany A Green; Teuvo L J Tammela; Joan Bailey-Wilson; Johanna Schleutker
Journal:  Int J Cancer       Date:  2011-04-20       Impact factor: 7.396

3.  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

Review 4.  Anoctamin/TMEM16 family members are Ca2+-activated Cl- channels.

Authors:  H Criss Hartzell; Kuai Yu; Qinhuan Xiao; Li-Ting Chien; Zhiqiang Qu
Journal:  J Physiol       Date:  2008-11-17       Impact factor: 5.182

5.  ANO7 is associated with aggressive prostate cancer.

Authors:  Elina Kaikkonen; Tommi Rantapero; Qin Zhang; Pekka Taimen; Virpi Laitinen; Markku Kallajoki; Dhanaprakash Jambulingam; Otto Ettala; Juha Knaapila; Peter J Boström; Gudrun Wahlström; Csilla Sipeky; Juha-Pekka Pursiheimo; Teuvo Tammela; Pirkko-Liisa Kellokumpu-Lehtinen; Vidal Fey; Lovise Maehle; Fredrik Wiklund; Gong-Hong Wei; Johanna Schleutker
Journal:  Int J Cancer       Date:  2018-09-22       Impact factor: 7.396

6.  The variant rs77559646 associated with aggressive prostate cancer disrupts ANO7 mRNA splicing and protein expression.

Authors:  Gudrun Wahlström; Samuel Heron; Matias Knuuttila; Elina Kaikkonen; Nea Tulonen; Olli Metsälä; Christoffer Löf; Otto Ettala; Peter J Boström; Pekka Taimen; Matti Poutanen; Johanna Schleutker
Journal:  Hum Mol Genet       Date:  2022-06-22       Impact factor: 5.121

7.  The interactome of the prostate-specific protein Anoctamin 7.

Authors:  Elina Kaikkonen; Aliisa Takala; Juha-Pekka Pursiheimo; Gudrun Wahlström; Johanna Schleutker
Journal:  Cancer Biomark       Date:  2020       Impact factor: 4.388

  7 in total

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