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Cytokine Candidate Genes Predict the Development of Secondary Lymphedema Following Breast Cancer Surgery

Identifieur interne : 002B94 ( Main/Exploration ); précédent : 002B93; suivant : 002B95

Cytokine Candidate Genes Predict the Development of Secondary Lymphedema Following Breast Cancer Surgery

Auteurs : Geraldine Leung ; Christina Baggott ; Claudia West ; Charles Elboim ; Steven M. Paul ; Bruce A. Cooper ; Gary Abrams ; Anand Dhruva ; Brian L. Schmidt ; Kord Kober ; John D. Merriman ; Heather Leutwyler ; John Neuhaus ; Dale Langford ; Betty J. Smoot ; Bradley E. Aouizerat ; Christine Miaskowski

Source :

RBID : PMC:3961780

Descripteurs français

English descriptors

Abstract

Abstract

Background: Lymphedema (LE) is a frequent complication following breast cancer treatment. While progress is being made in the identification of phenotypic risk factors for the development of LE, little information is available on the molecular characterization of LE. The purpose of this study was to determine if variations in pro- and anti-inflammatory cytokine genes were associated with LE following breast cancer treatment.

Methods and Results: Breast cancer patients completed a number of self-report questionnaires. LE was evaluated using bioimpedance spectroscopy. Genotyping was done using a custom genotyping array. No differences were found between patients with (n=155) and without LE (n=387) for the majority of the demographic and clinical characteristics. Patients with LE had a significantly higher body mass index, more advanced disease, and a higher number of lymph nodes removed. Genetic associations were identified for three genes (i.e., interleukin (IL4) 4 (rs2227284), IL 10 (rs1518111), and nuclear kappa factor beta 2 (NFKB2 (rs1056890)) associated with inflammatory responses.

Conclusions: These genetic associations suggest a role for a number of pro- and anti-inflammatory genes in the development of LE following breast cancer treatment.


Url:
DOI: 10.1089/lrb.2013.0024
PubMed: 24502445
PubMed Central: 3961780


Affiliations:


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Le document en format XML

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<name sortKey="Schmidt, Brian L" sort="Schmidt, Brian L" uniqKey="Schmidt B" first="Brian L." last="Schmidt">Brian L. Schmidt</name>
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<title level="j">Lymphatic Research and Biology</title>
<idno type="ISSN">1539-6851</idno>
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<keywords scheme="KwdEn" xml:lang="en">
<term>Adult</term>
<term>Aged</term>
<term>Breast Neoplasms (genetics)</term>
<term>Breast Neoplasms (surgery)</term>
<term>Cytokines (genetics)</term>
<term>Electric Impedance</term>
<term>Female</term>
<term>Genetic Predisposition to Disease (genetics)</term>
<term>Genotype</term>
<term>Humans</term>
<term>Lymphedema (etiology)</term>
<term>Lymphedema (genetics)</term>
<term>Mastectomy (adverse effects)</term>
<term>Middle Aged</term>
<term>Oligonucleotide Array Sequence Analysis</term>
<term>Polymorphism, Single Nucleotide</term>
<term>Surveys and Questionnaires</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Cytokines (génétique)</term>
<term>Enquêtes et questionnaires</term>
<term>Femelle</term>
<term>Génotype</term>
<term>Humains</term>
<term>Impédance électrique</term>
<term>Lymphoedème (génétique)</term>
<term>Lymphoedème (étiologie)</term>
<term>Mastectomie (effets indésirables)</term>
<term>Polymorphisme de nucléotide simple</term>
<term>Prédisposition génétique à une maladie (génétique)</term>
<term>Sujet âgé</term>
<term>Séquençage par oligonucléotides en batterie</term>
<term>Tumeurs du sein ()</term>
<term>Tumeurs du sein (génétique)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Cytokines</term>
</keywords>
<keywords scheme="MESH" qualifier="adverse effects" xml:lang="en">
<term>Mastectomy</term>
</keywords>
<keywords scheme="MESH" qualifier="effets indésirables" xml:lang="fr">
<term>Mastectomie</term>
</keywords>
<keywords scheme="MESH" qualifier="etiology" xml:lang="en">
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Breast Neoplasms</term>
<term>Genetic Predisposition to Disease</term>
<term>Lymphedema</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Cytokines</term>
<term>Lymphoedème</term>
<term>Prédisposition génétique à une maladie</term>
<term>Tumeurs du sein</term>
</keywords>
<keywords scheme="MESH" qualifier="surgery" xml:lang="en">
<term>Breast Neoplasms</term>
</keywords>
<keywords scheme="MESH" qualifier="étiologie" xml:lang="fr">
<term>Lymphoedème</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adult</term>
<term>Aged</term>
<term>Electric Impedance</term>
<term>Female</term>
<term>Genotype</term>
<term>Humans</term>
<term>Middle Aged</term>
<term>Oligonucleotide Array Sequence Analysis</term>
<term>Polymorphism, Single Nucleotide</term>
<term>Surveys and Questionnaires</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Enquêtes et questionnaires</term>
<term>Femelle</term>
<term>Génotype</term>
<term>Humains</term>
<term>Impédance électrique</term>
<term>Polymorphisme de nucléotide simple</term>
<term>Sujet âgé</term>
<term>Séquençage par oligonucléotides en batterie</term>
<term>Tumeurs du sein</term>
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<div type="abstract" xml:lang="en">
<title>Abstract</title>
<p>
<bold>
<italic>Background:</italic>
</bold>
Lymphedema (LE) is a frequent complication following breast cancer treatment. While progress is being made in the identification of phenotypic risk factors for the development of LE, little information is available on the molecular characterization of LE. The purpose of this study was to determine if variations in pro- and anti-inflammatory cytokine genes were associated with LE following breast cancer treatment.</p>
<p>
<bold>
<italic>Methods and Results:</italic>
</bold>
Breast cancer patients completed a number of self-report questionnaires. LE was evaluated using bioimpedance spectroscopy. Genotyping was done using a custom genotyping array. No differences were found between patients with (
<italic>n</italic>
=155) and without LE (
<italic>n</italic>
=387) for the majority of the demographic and clinical characteristics. Patients with LE had a significantly higher body mass index, more advanced disease, and a higher number of lymph nodes removed. Genetic associations were identified for three genes (i.e., interleukin (IL4) 4 (rs2227284), IL 10 (rs1518111), and nuclear kappa factor beta 2 (NFKB2 (rs1056890)) associated with inflammatory responses.</p>
<p>
<bold>
<italic>Conclusions:</italic>
</bold>
These genetic associations suggest a role for a number of pro- and anti-inflammatory genes in the development of LE following breast cancer treatment.</p>
</div>
</front>
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<name sortKey="Miaskowski, Christine" sort="Miaskowski, Christine" uniqKey="Miaskowski C" first="Christine" last="Miaskowski">Christine Miaskowski</name>
<name sortKey="Neuhaus, John" sort="Neuhaus, John" uniqKey="Neuhaus J" first="John" last="Neuhaus">John Neuhaus</name>
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<name sortKey="Schmidt, Brian L" sort="Schmidt, Brian L" uniqKey="Schmidt B" first="Brian L." last="Schmidt">Brian L. Schmidt</name>
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