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Detection of protein alterations in male breast cancer using two dimensional gel electrophoresis and mass spectrometry: the involvement of several pathways in tumorigenesis.

Identifieur interne : 000047 ( Main/Exploration ); précédent : 000046; suivant : 000048

Detection of protein alterations in male breast cancer using two dimensional gel electrophoresis and mass spectrometry: the involvement of several pathways in tumorigenesis.

Auteurs : Karim Chahed [Tunisie] ; Maria Kabbage ; Bechr Hamrita ; Christelle Lemaitre Guillier ; Mounir Trimeche ; Sami Remadi ; Laurence Ehret-Sabatier ; Lotfi Chouchane

Source :

RBID : pubmed:17996735

Descripteurs français

English descriptors

Abstract

BACKGROUND

Little emphasis has been placed today on the elucidation of protein alterations in male breast carcinogenesis.

METHODS

Protein extracts were subjected to both isoelectric focusing (IEF) and non-equilibrium pH gradient electrophoretic (NEPHGE) analyses. Differentially expressed proteins in tumor tissues were identified by matrix assisted laser desorption /ionization time of flight (MALDI-TOF) mass spectrometry and database search.

RESULTS

Some of the alterations involve variations in the expression of cytokeratins 8, 18 and 19. More interestingly, tropomyosin1, a protein known to play a role in suppression of the malignant phenotype, was found to be under-expressed in cancer tissues, implicating a possible pivotal role for this protein in male breast carcinogenesis. Co-upregulation of molecular chaperones (heat shock protein HSP27 and protein disulfide isomerase), stress related proteins (peroxiredoxin 1 and peptidylprolyl isomerase A) and glycolytic enzymes (enolase 1) occurred also in male breast tumors. Some of the remaining alterations include proteins involved in invasion and metastasis, such as galectin 1 and cathepsin D.

CONCLUSIONS

The present study represents a first proteomic investigation of protein alterations in infiltrating ductal carcinomas (IDCA) of the male breast. A number of protein alterations in tumor tissues have been characterised thus, providing new insights into the molecular mechanisms underlying this disease.


DOI: 10.1016/j.cca.2007.10.018
PubMed: 17996735


Affiliations:


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Le document en format XML

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<name sortKey="Kabbage, Maria" sort="Kabbage, Maria" uniqKey="Kabbage M" first="Maria" last="Kabbage">Maria Kabbage</name>
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<name sortKey="Hamrita, Bechr" sort="Hamrita, Bechr" uniqKey="Hamrita B" first="Bechr" last="Hamrita">Bechr Hamrita</name>
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<name sortKey="Guillier, Christelle Lemaitre" sort="Guillier, Christelle Lemaitre" uniqKey="Guillier C" first="Christelle Lemaitre" last="Guillier">Christelle Lemaitre Guillier</name>
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<name sortKey="Trimeche, Mounir" sort="Trimeche, Mounir" uniqKey="Trimeche M" first="Mounir" last="Trimeche">Mounir Trimeche</name>
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<name sortKey="Remadi, Sami" sort="Remadi, Sami" uniqKey="Remadi S" first="Sami" last="Remadi">Sami Remadi</name>
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<name sortKey="Ehret Sabatier, Laurence" sort="Ehret Sabatier, Laurence" uniqKey="Ehret Sabatier L" first="Laurence" last="Ehret-Sabatier">Laurence Ehret-Sabatier</name>
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<name sortKey="Kabbage, Maria" sort="Kabbage, Maria" uniqKey="Kabbage M" first="Maria" last="Kabbage">Maria Kabbage</name>
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<name sortKey="Hamrita, Bechr" sort="Hamrita, Bechr" uniqKey="Hamrita B" first="Bechr" last="Hamrita">Bechr Hamrita</name>
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<name sortKey="Guillier, Christelle Lemaitre" sort="Guillier, Christelle Lemaitre" uniqKey="Guillier C" first="Christelle Lemaitre" last="Guillier">Christelle Lemaitre Guillier</name>
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<name sortKey="Trimeche, Mounir" sort="Trimeche, Mounir" uniqKey="Trimeche M" first="Mounir" last="Trimeche">Mounir Trimeche</name>
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<name sortKey="Remadi, Sami" sort="Remadi, Sami" uniqKey="Remadi S" first="Sami" last="Remadi">Sami Remadi</name>
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<author>
<name sortKey="Ehret Sabatier, Laurence" sort="Ehret Sabatier, Laurence" uniqKey="Ehret Sabatier L" first="Laurence" last="Ehret-Sabatier">Laurence Ehret-Sabatier</name>
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<name sortKey="Chouchane, Lotfi" sort="Chouchane, Lotfi" uniqKey="Chouchane L" first="Lotfi" last="Chouchane">Lotfi Chouchane</name>
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<title level="j">Clinica chimica acta; international journal of clinical chemistry</title>
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<term>Amino Acid Sequence (MeSH)</term>
<term>Breast Neoplasms, Male (metabolism)</term>
<term>Breast Neoplasms, Male (pathology)</term>
<term>Cell Transformation, Neoplastic (metabolism)</term>
<term>Cell Transformation, Neoplastic (pathology)</term>
<term>Electrophoresis, Gel, Two-Dimensional (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Molecular Sequence Data (MeSH)</term>
<term>Neoplasm Proteins (chemistry)</term>
<term>Neoplasm Proteins (metabolism)</term>
<term>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization (MeSH)</term>
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<term>Adulte d'âge moyen (MeSH)</term>
<term>Données de séquences moléculaires (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Mâle (MeSH)</term>
<term>Protéines tumorales (composition chimique)</term>
<term>Protéines tumorales (métabolisme)</term>
<term>Spectrométrie de masse MALDI (MeSH)</term>
<term>Séquence d'acides aminés (MeSH)</term>
<term>Transformation cellulaire néoplasique (anatomopathologie)</term>
<term>Transformation cellulaire néoplasique (métabolisme)</term>
<term>Tumeur du sein de l'homme (anatomopathologie)</term>
<term>Tumeur du sein de l'homme (métabolisme)</term>
<term>Électrophorèse bidimensionnelle sur gel (MeSH)</term>
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<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en">
<term>Neoplasm Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr">
<term>Transformation cellulaire néoplasique</term>
<term>Tumeur du sein de l'homme</term>
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<keywords scheme="MESH" qualifier="composition chimique" xml:lang="fr">
<term>Protéines tumorales</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Breast Neoplasms, Male</term>
<term>Cell Transformation, Neoplastic</term>
<term>Neoplasm Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Protéines tumorales</term>
<term>Transformation cellulaire néoplasique</term>
<term>Tumeur du sein de l'homme</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Breast Neoplasms, Male</term>
<term>Cell Transformation, Neoplastic</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Amino Acid Sequence</term>
<term>Electrophoresis, Gel, Two-Dimensional</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Molecular Sequence Data</term>
<term>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</term>
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<keywords scheme="MESH" xml:lang="fr">
<term>Adulte d'âge moyen</term>
<term>Données de séquences moléculaires</term>
<term>Humains</term>
<term>Mâle</term>
<term>Spectrométrie de masse MALDI</term>
<term>Séquence d'acides aminés</term>
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<front>
<div type="abstract" xml:lang="en">
<p>
<b>BACKGROUND</b>
</p>
<p>Little emphasis has been placed today on the elucidation of protein alterations in male breast carcinogenesis.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>METHODS</b>
</p>
<p>Protein extracts were subjected to both isoelectric focusing (IEF) and non-equilibrium pH gradient electrophoretic (NEPHGE) analyses. Differentially expressed proteins in tumor tissues were identified by matrix assisted laser desorption /ionization time of flight (MALDI-TOF) mass spectrometry and database search.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>Some of the alterations involve variations in the expression of cytokeratins 8, 18 and 19. More interestingly, tropomyosin1, a protein known to play a role in suppression of the malignant phenotype, was found to be under-expressed in cancer tissues, implicating a possible pivotal role for this protein in male breast carcinogenesis. Co-upregulation of molecular chaperones (heat shock protein HSP27 and protein disulfide isomerase), stress related proteins (peroxiredoxin 1 and peptidylprolyl isomerase A) and glycolytic enzymes (enolase 1) occurred also in male breast tumors. Some of the remaining alterations include proteins involved in invasion and metastasis, such as galectin 1 and cathepsin D.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>The present study represents a first proteomic investigation of protein alterations in infiltrating ductal carcinomas (IDCA) of the male breast. A number of protein alterations in tumor tissues have been characterised thus, providing new insights into the molecular mechanisms underlying this disease.</p>
</div>
</front>
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<name sortKey="Guillier, Christelle Lemaitre" sort="Guillier, Christelle Lemaitre" uniqKey="Guillier C" first="Christelle Lemaitre" last="Guillier">Christelle Lemaitre Guillier</name>
<name sortKey="Hamrita, Bechr" sort="Hamrita, Bechr" uniqKey="Hamrita B" first="Bechr" last="Hamrita">Bechr Hamrita</name>
<name sortKey="Kabbage, Maria" sort="Kabbage, Maria" uniqKey="Kabbage M" first="Maria" last="Kabbage">Maria Kabbage</name>
<name sortKey="Remadi, Sami" sort="Remadi, Sami" uniqKey="Remadi S" first="Sami" last="Remadi">Sami Remadi</name>
<name sortKey="Trimeche, Mounir" sort="Trimeche, Mounir" uniqKey="Trimeche M" first="Mounir" last="Trimeche">Mounir Trimeche</name>
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<name sortKey="Chahed, Karim" sort="Chahed, Karim" uniqKey="Chahed K" first="Karim" last="Chahed">Karim Chahed</name>
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