A role for the collagen I/III and MMP-1/-13 genes in primary inguinal hernia?

<p>Abstract</p> <p>Background</p> <p>Abnormal collagen metabolism is thought to play an important role in the development of primary inguinal hernia. This is underlined by detection of altered collagen metabolism and structural changes of the tissue in patients with pri...

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Main Authors: Klinge Uwe, Rosch Raphael, Si Zhongyi, Junge Karsten, Klosterhalfen Bernd, Schumpelick Volker
Format: Article
Language:English
Published: BMC 2002-02-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/3/2
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spelling doaj-5f6430c5cd8d46efa24079e4897ec1dc2021-04-02T09:36:34ZengBMCBMC Medical Genetics1471-23502002-02-0131210.1186/1471-2350-3-2A role for the collagen I/III and MMP-1/-13 genes in primary inguinal hernia?Klinge UweRosch RaphaelSi ZhongyiJunge KarstenKlosterhalfen BerndSchumpelick Volker<p>Abstract</p> <p>Background</p> <p>Abnormal collagen metabolism is thought to play an important role in the development of primary inguinal hernia. This is underlined by detection of altered collagen metabolism and structural changes of the tissue in patients with primary inguinal hernia. However, it is still unknown whether these alterations reflect a basic dysfunction of the collagen synthesis, or of collagen degradation.</p> <p>Methods</p> <p>In the present study, we analysed type I and type III procollagen messenger ribonucleic acid (mRNA) and MMP-1 and MMP-13 mRNA in cultured fibroblasts from the skin of patients with primary inguinal hernia, and from patients without hernia (controls) by reverse transcription polymerase chain reaction (RT-PCR) and Northern Blot.</p> <p>Results</p> <p>The results indicated that the ratio of type I to type III procollagen mRNA was decreased in patients with primary hernia, showing significant differences as compared to controls (p = 0.01). This decrease was mainly due to the increase of type III procollagen mRNA. Furthermore, RT-PCR analysis revealed that the expression of MMP-1 mRNA in patients with primary hernia is equivalent to that of controls (p > 0.05). In addition, MMP-13 mRNA is expressed neither in patients with primary hernia nor in controls.</p> <p>Conclusion</p> <p>We concluded that abnormal change of type I and type III collagen mRNAs contribute to the development of primary inguinal hernia, whereas the expressions of MMP-1 and MMP-13 mRNA appears not to be involved in the development of primary inguinal hernia. Thus, the knowledge on the transcriptional regulation of collagen in patients with primary inguinal hernia may help to understand the pathogenesis of primary inguinal hernia, and implies new therapeutic strategies for this disease.</p> http://www.biomedcentral.com/1471-2350/3/2
collection DOAJ
language English
format Article
sources DOAJ
author Klinge Uwe
Rosch Raphael
Si Zhongyi
Junge Karsten
Klosterhalfen Bernd
Schumpelick Volker
spellingShingle Klinge Uwe
Rosch Raphael
Si Zhongyi
Junge Karsten
Klosterhalfen Bernd
Schumpelick Volker
A role for the collagen I/III and MMP-1/-13 genes in primary inguinal hernia?
BMC Medical Genetics
author_facet Klinge Uwe
Rosch Raphael
Si Zhongyi
Junge Karsten
Klosterhalfen Bernd
Schumpelick Volker
author_sort Klinge Uwe
title A role for the collagen I/III and MMP-1/-13 genes in primary inguinal hernia?
title_short A role for the collagen I/III and MMP-1/-13 genes in primary inguinal hernia?
title_full A role for the collagen I/III and MMP-1/-13 genes in primary inguinal hernia?
title_fullStr A role for the collagen I/III and MMP-1/-13 genes in primary inguinal hernia?
title_full_unstemmed A role for the collagen I/III and MMP-1/-13 genes in primary inguinal hernia?
title_sort role for the collagen i/iii and mmp-1/-13 genes in primary inguinal hernia?
publisher BMC
series BMC Medical Genetics
issn 1471-2350
publishDate 2002-02-01
description <p>Abstract</p> <p>Background</p> <p>Abnormal collagen metabolism is thought to play an important role in the development of primary inguinal hernia. This is underlined by detection of altered collagen metabolism and structural changes of the tissue in patients with primary inguinal hernia. However, it is still unknown whether these alterations reflect a basic dysfunction of the collagen synthesis, or of collagen degradation.</p> <p>Methods</p> <p>In the present study, we analysed type I and type III procollagen messenger ribonucleic acid (mRNA) and MMP-1 and MMP-13 mRNA in cultured fibroblasts from the skin of patients with primary inguinal hernia, and from patients without hernia (controls) by reverse transcription polymerase chain reaction (RT-PCR) and Northern Blot.</p> <p>Results</p> <p>The results indicated that the ratio of type I to type III procollagen mRNA was decreased in patients with primary hernia, showing significant differences as compared to controls (p = 0.01). This decrease was mainly due to the increase of type III procollagen mRNA. Furthermore, RT-PCR analysis revealed that the expression of MMP-1 mRNA in patients with primary hernia is equivalent to that of controls (p > 0.05). In addition, MMP-13 mRNA is expressed neither in patients with primary hernia nor in controls.</p> <p>Conclusion</p> <p>We concluded that abnormal change of type I and type III collagen mRNAs contribute to the development of primary inguinal hernia, whereas the expressions of MMP-1 and MMP-13 mRNA appears not to be involved in the development of primary inguinal hernia. Thus, the knowledge on the transcriptional regulation of collagen in patients with primary inguinal hernia may help to understand the pathogenesis of primary inguinal hernia, and implies new therapeutic strategies for this disease.</p>
url http://www.biomedcentral.com/1471-2350/3/2
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