Identification of a down-regulated mRNA transcript in corpus cavernosum from diabetic patients with erectile dysfunction.

M. V. Autieri, A. Melman, G. J. Christ

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Fifty per cent of men with diabetes have erectile dysfunction. Previous studies demonstrated that cultured smooth muscle cells from corpus cavernosum display significantly altered K+ channel function, PGE-induced cAMP accumulation, and endothelin-1 induced Ca2+ mobilization that are consistent with the pathophysiology of erectile dysfunction. Since defects in signal transduction frequently lead to altered gene expression, we examined differences in gene expression in corporal tissue excised from three diabetic patients with erectile dysfunction function and one patient with neurogenic erectile dysfunction. Using differential display, we identify a transcript expressed in tissue derived from the patient with impotence secondary to a radical prostectomy, but which was greatly reduced or absent in corporal tissue from all three diabetic patients examined. DNA sequence analysis indicates that this transcript has no significant homology to sequences presently deposited in the GenBank database. This suggests that altered gene expression may play a significant part in the etiology of erectile dysfunction.

Original languageEnglish (US)
Pages (from-to)69-73
Number of pages5
JournalInternational Journal of Impotence Research
Volume8
Issue number2
StatePublished - Jun 1996

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Erectile Dysfunction
Messenger RNA
Gene Expression
Nucleic Acid Databases
Endothelin-1
Sequence Homology
Prostaglandins E
DNA Sequence Analysis
Smooth Muscle Myocytes
Signal Transduction
Databases

ASJC Scopus subject areas

  • Urology

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Identification of a down-regulated mRNA transcript in corpus cavernosum from diabetic patients with erectile dysfunction. / Autieri, M. V.; Melman, A.; Christ, G. J.

In: International Journal of Impotence Research, Vol. 8, No. 2, 06.1996, p. 69-73.

Research output: Contribution to journalArticle

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