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A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci

Identifieur interne : 000509 ( Main/Exploration ); précédent : 000508; suivant : 000510

A genome wide SNP genotyping study in the Tunisian population: specific reporting on a subset of common breast cancer risk loci

Auteurs : Yosr Hamdi ; Mariem Ben Rekaya ; Shan Jingxuan [Qatar] ; Majdi Nagara ; Olfa Messaoud ; Amel Benammar Elgaaied [Tunisie] ; Ridha Mrad [Tunisie] ; Lotfi Chouchane [Qatar] ; Mohamed Samir Boubaker ; Sonia Abdelhak ; Hamouda Boussen [Tunisie] ; Lilia Romdhane [Tunisie]

Source :

RBID : PMC:6310952

Descripteurs français

English descriptors

Abstract

Background

Breast cancer is the most common cancer in women worldwide. Around 50% of breast cancer familial risk has been so far explained by known susceptibility alleles with variable levels of risk and prevalence. The vast majority of these breast cancer associated variations reported to date are from populations of European ancestry. In spite of its heterogeneity and genetic wealth, North-African populations have not been studied by the HapMap and the 1000Genomes projects. Thus, very little is known about the genetic architecture of these populations.

Methods

This study aimed to investigate a subset of common breast cancer loci in the general Tunisian population and to compare their genetic composition to those of other ethnic groups. We undertook a genome-wide haplotype study by genotyping 135 Tunisian subjects using the Affymetrix 6.0-Array. We compared Tunisian allele frequencies and linkage disequilibrium patterns to those of HapMap populations and we performed a comprehensive assessment of the functional effects of several selected variants.

Results

Haplotype analyses showed that at risk haplotypes on 2p24, 4q21, 6q25, 9q31, 10q26, 11p15, 11q13 and 14q32 loci are considerably frequent in the Tunisian population (> 20%). Allele frequency comparison showed that the frequency of rs13329835 is significantly different between Tunisian and all other HapMap populations. LD-blocks and Principle Component Analysis revealed that the genetic characteristics of breast cancer variants in the Tunisian, and so probably the North-African populations, are more similar to those of Europeans than Africans.

Using eQTl analysis, we characterized rs9911630 as the most strongly expression-associated SNP that seems to affect the expression levels of BRCA1 and two long non coding RNAs (NBR2 and LINC008854). Additional in-silico analysis also suggested a potential functional significance of this variant.

Conclusions

We illustrated the utility of combining haplotype analysis in diverse ethnic groups with functional analysis to explore breast cancer genetic architecture in Tunisia. Results presented in this study provide the first report on a large number of common breast cancer genetic polymorphisms in the Tunisian population which may establish a baseline database to guide future association studies in North Africa.

Electronic supplementary material

The online version of this article (10.1186/s12885-018-5133-8) contains supplementary material, which is available to authorized users.


Url:
DOI: 10.1186/s12885-018-5133-8
PubMed: 30594178
PubMed Central: 6310952


Affiliations:


Links toward previous steps (curation, corpus...)


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<title level="j">BMC Cancer</title>
<idno type="eISSN">1471-2407</idno>
<imprint>
<date when="2018">2018</date>
</imprint>
</series>
</biblStruct>
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<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Adult (MeSH)</term>
<term>African Continental Ancestry Group (genetics)</term>
<term>Breast Neoplasms (genetics)</term>
<term>Computer Simulation (MeSH)</term>
<term>Female (MeSH)</term>
<term>Gene Frequency (genetics)</term>
<term>Genetic Loci (genetics)</term>
<term>Genetic Predisposition to Disease (MeSH)</term>
<term>Genome-Wide Association Study (MeSH)</term>
<term>Haplotypes (genetics)</term>
<term>Healthy Volunteers (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Linkage Disequilibrium (genetics)</term>
<term>Male (MeSH)</term>
<term>Middle Aged (MeSH)</term>
<term>Polymorphism, Single Nucleotide (MeSH)</term>
<term>Tunisia (MeSH)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Adulte (MeSH)</term>
<term>Adulte d'âge moyen (MeSH)</term>
<term>Déséquilibre de liaison (génétique)</term>
<term>Femelle (MeSH)</term>
<term>Fréquence d'allèle (génétique)</term>
<term>Haplotypes (génétique)</term>
<term>Humains (MeSH)</term>
<term>Locus génétiques (génétique)</term>
<term>Mâle (MeSH)</term>
<term>Polymorphisme de nucléotide simple (MeSH)</term>
<term>Population d'origine africaine (génétique)</term>
<term>Prédisposition génétique à une maladie (MeSH)</term>
<term>Simulation numérique (MeSH)</term>
<term>Tumeurs du sein (génétique)</term>
<term>Tunisie (MeSH)</term>
<term>Volontaires sains (MeSH)</term>
<term>Étude d'association pangénomique (MeSH)</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en">
<term>Tunisia</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>African Continental Ancestry Group</term>
<term>Breast Neoplasms</term>
<term>Gene Frequency</term>
<term>Genetic Loci</term>
<term>Haplotypes</term>
<term>Linkage Disequilibrium</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Déséquilibre de liaison</term>
<term>Fréquence d'allèle</term>
<term>Haplotypes</term>
<term>Locus génétiques</term>
<term>Population d'origine africaine</term>
<term>Tumeurs du sein</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Adult</term>
<term>Computer Simulation</term>
<term>Female</term>
<term>Genetic Predisposition to Disease</term>
<term>Genome-Wide Association Study</term>
<term>Healthy Volunteers</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Polymorphism, Single Nucleotide</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Femelle</term>
<term>Humains</term>
<term>Mâle</term>
<term>Polymorphisme de nucléotide simple</term>
<term>Prédisposition génétique à une maladie</term>
<term>Simulation numérique</term>
<term>Tunisie</term>
<term>Volontaires sains</term>
<term>Étude d'association pangénomique</term>
</keywords>
<keywords scheme="Wicri" type="geographic" xml:lang="fr">
<term>Tunisie</term>
</keywords>
</textClass>
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</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<sec>
<title>Background</title>
<p id="Par1">Breast cancer is the most common cancer in women worldwide. Around 50% of breast cancer familial risk has been so far explained by known susceptibility alleles with variable levels of risk and prevalence. The vast majority of these breast cancer associated variations reported to date are from populations of European ancestry. In spite of its heterogeneity and genetic wealth, North-African populations have not been studied by the HapMap and the 1000Genomes projects. Thus, very little is known about the genetic architecture of these populations.</p>
</sec>
<sec>
<title>Methods</title>
<p id="Par2">This study aimed to investigate a subset of common breast cancer loci in the general Tunisian population and to compare their genetic composition to those of other ethnic groups. We undertook a genome-wide haplotype study by genotyping 135 Tunisian subjects using the Affymetrix 6.0-Array. We compared Tunisian allele frequencies and linkage disequilibrium patterns to those of HapMap populations and we performed a comprehensive assessment of the functional effects of several selected variants.</p>
</sec>
<sec>
<title>Results</title>
<p id="Par3">Haplotype analyses showed that at risk haplotypes on 2p24, 4q21, 6q25, 9q31, 10q26, 11p15, 11q13 and 14q32 loci are considerably frequent in the Tunisian population (> 20%). Allele frequency comparison showed that the frequency of rs13329835 is significantly different between Tunisian and all other HapMap populations. LD-blocks and Principle Component Analysis revealed that the genetic characteristics of breast cancer variants in the Tunisian, and so probably the North-African populations, are more similar to those of Europeans than Africans.</p>
<p id="Par4">Using eQTl analysis, we characterized rs9911630 as the most strongly expression-associated SNP that seems to affect the expression levels of
<italic>BRCA1</italic>
and two long non coding RNAs (
<italic>NBR2</italic>
and
<italic>LINC008854</italic>
). Additional
<italic>in-silico</italic>
analysis also suggested a potential functional significance of this variant.</p>
</sec>
<sec>
<title>Conclusions</title>
<p id="Par5">We illustrated the utility of combining haplotype analysis in diverse ethnic groups with functional analysis to explore breast cancer genetic architecture in Tunisia. Results presented in this study provide the first report on a large number of common breast cancer genetic polymorphisms in the Tunisian population which may establish a baseline database to guide future association studies in North Africa.</p>
</sec>
<sec>
<title>Electronic supplementary material</title>
<p>The online version of this article (10.1186/s12885-018-5133-8) contains supplementary material, which is available to authorized users.</p>
</sec>
</div>
</front>
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<author>
<name sortKey="Ziegler, Rg" uniqKey="Ziegler R">RG Ziegler</name>
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<author>
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</author>
<author>
<name sortKey="Zhuang, L" uniqKey="Zhuang L">L Zhuang</name>
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<author>
<name sortKey="Gan, B" uniqKey="Gan B">B Gan</name>
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</analytic>
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<name sortKey="Luo, S" uniqKey="Luo S">S Luo</name>
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<author>
<name sortKey="Han, X" uniqKey="Han X">X Han</name>
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<author>
<name sortKey="Wu, B" uniqKey="Wu B">B Wu</name>
</author>
<author>
<name sortKey="Xu, R" uniqKey="Xu R">R Xu</name>
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<author>
<name sortKey="Liu, W" uniqKey="Liu W">W Liu</name>
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<author>
<name sortKey="Yan, P" uniqKey="Yan P">P Yan</name>
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<name sortKey="Hung, Cl" uniqKey="Hung C">CL Hung</name>
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</author>
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<name sortKey="Chen, Hw" uniqKey="Chen H">HW Chen</name>
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<name sortKey="Srivastava, S" uniqKey="Srivastava S">S Srivastava</name>
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<author>
<name sortKey="Zhuang, L" uniqKey="Zhuang L">L Zhuang</name>
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<author>
<name sortKey="Gan, B" uniqKey="Gan B">B Gan</name>
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<author>
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<author>
<name sortKey="Tsay, M" uniqKey="Tsay M">M Tsay</name>
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</analytic>
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<name sortKey="Chin, Ar" uniqKey="Chin A">AR Chin</name>
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<name sortKey="Fong, My" uniqKey="Fong M">MY Fong</name>
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</TEI>
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<list>
<country>
<li>Qatar</li>
<li>Tunisie</li>
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</list>
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<name sortKey="Abdelhak, Sonia" sort="Abdelhak, Sonia" uniqKey="Abdelhak S" first="Sonia" last="Abdelhak">Sonia Abdelhak</name>
<name sortKey="Ben Rekaya, Mariem" sort="Ben Rekaya, Mariem" uniqKey="Ben Rekaya M" first="Mariem" last="Ben Rekaya">Mariem Ben Rekaya</name>
<name sortKey="Boubaker, Mohamed Samir" sort="Boubaker, Mohamed Samir" uniqKey="Boubaker M" first="Mohamed Samir" last="Boubaker">Mohamed Samir Boubaker</name>
<name sortKey="Hamdi, Yosr" sort="Hamdi, Yosr" uniqKey="Hamdi Y" first="Yosr" last="Hamdi">Yosr Hamdi</name>
<name sortKey="Messaoud, Olfa" sort="Messaoud, Olfa" uniqKey="Messaoud O" first="Olfa" last="Messaoud">Olfa Messaoud</name>
<name sortKey="Nagara, Majdi" sort="Nagara, Majdi" uniqKey="Nagara M" first="Majdi" last="Nagara">Majdi Nagara</name>
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<name sortKey="Jingxuan, Shan" sort="Jingxuan, Shan" uniqKey="Jingxuan S" first="Shan" last="Jingxuan">Shan Jingxuan</name>
</noRegion>
<name sortKey="Chouchane, Lotfi" sort="Chouchane, Lotfi" uniqKey="Chouchane L" first="Lotfi" last="Chouchane">Lotfi Chouchane</name>
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<name sortKey="Benammar Elgaaied, Amel" sort="Benammar Elgaaied, Amel" uniqKey="Benammar Elgaaied A" first="Amel" last="Benammar Elgaaied">Amel Benammar Elgaaied</name>
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<name sortKey="Boussen, Hamouda" sort="Boussen, Hamouda" uniqKey="Boussen H" first="Hamouda" last="Boussen">Hamouda Boussen</name>
<name sortKey="Mrad, Ridha" sort="Mrad, Ridha" uniqKey="Mrad R" first="Ridha" last="Mrad">Ridha Mrad</name>
<name sortKey="Romdhane, Lilia" sort="Romdhane, Lilia" uniqKey="Romdhane L" first="Lilia" last="Romdhane">Lilia Romdhane</name>
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</tree>
</affiliations>
</record>

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