Abstract
A prostate-specific gene, PCGEM1, was identified by differential display analysis of paired normal and prostate cancer tissues. Multiple tissue Northern blot analysis revealed that PCGEM1 was expressed exclusively in human prostate tissue. Analysis of PCGEM1 expression in matched normal and primary tumor specimens revealed tumor-associated overexpression in 84% of patients with prostate cancer by in situ hybridization assay and in 56% of patients by reverse transcription-PCR assay. Among various prostate cancer cell lines analyzed, PCGEM1 expression was detected only in the androgen receptor-positive cell line LNCaP. Extensive DNA sequence analysis of the PCGEM1 cDNA and genomic DNA revealed that PCGEM1 lacks protein-coding capacity and suggests that it may belong to an emerging class of noncoding RNAs, also called "riboregulators." The PCGEM1 locus was mapped to chromosome 2q32. Taken together, the remarkable prostate-tissue specificity and androgen-dependent expression of PCGEM1 as well as its elevated expression in a significant percentage of tumor tissues suggest specific functions of PCGEM1 in the biology and tumorigenesis of the prostate gland.
MeSH Terms
Androgens/physiology
Animals
Base Sequence
Cell Division/genetics
Chromosome Mapping
Chromosomes, Human, Pair 2
DNA, Complementary
Epithelial Cells/cytology
Gene Expression Regulation, Neoplastic
Humans
Male
Mice
Mice, Nude
Molecular Sequence Data
Neoplasm Proteins/genetics
Prostate/cytology
Prostatic Neoplasms/genetics,pathology
RNA, Long Noncoding
RNA, Untranslated
Tumor Cells, Cultured
Chemicals
Androgens
DNA, Complementary
Neoplasm Proteins
PCGEM1 non-coding RNA, human
RNA, Long Noncoding
RNA, Untranslated
Authors & Affiliations
15 authors, click to expand affiliations / ORCID
Srikantan V
Center for Prostate Disease Research, Department of Surgery, Uniformed Services University of the Health Sciences, Bethesda, MD 20814-4799, USA.
Zou Z
Petrovics G
Xu L
Augustus M
Davis L
Livezey J R
Connell T
Sesterhenn I A
Yoshino K
Buzard G S
Mostofi F K
McLeod D G
Moul J W
Srivastava S
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