Glutathione S-transferase M1 (GSTM1) and T1 (GSTT1) variants and breast cancer risk in Burkina Faso

Background and objective Breast cancer remains the most common cause of cancer mortality in women. The aim of this study was to investigate associations between genetic variability in GSTM1 and GSTT1 and susceptibility to breast cancer. Methods Genomic DNA was extracted from blood samples for 80 cas...

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Published inBiomolecular concepts Vol. 10; no. 1; p. 175
Main Authors Kiendrebeogo, Isabelle Touwendpoulimdé, Zoure, Abdou Azaque, Sorgho, Pegdwendé Abel, Yonli, Albert Théophane, Djigma, Florencia Wendkuuni, Ouattara, Abdoul Karim, Sombie, Herman Karim, Tovo, Sessi Frida, Yelemkoure, Edwige T, Bambara, Aboubacar Hierrhum, Sawadogo, Alexis Yobi, Bakri, Youssef, Simpore, Jacques
Format Journal Article
LanguageEnglish
Published Germany 09.11.2019
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Abstract Background and objective Breast cancer remains the most common cause of cancer mortality in women. The aim of this study was to investigate associations between genetic variability in GSTM1 and GSTT1 and susceptibility to breast cancer. Methods Genomic DNA was extracted from blood samples for 80 cases of histologically diagnosed breast cancer and 100 control subjects. Genotyping analyses were performed by PCR-based methods. Associations between specific genotypes and the development of breast cancer were examined using logistic regression to calculate odds ratios [1] and 95% confidence intervals (95%CI). Results No correlation was found between GSTM1-null and breast cancer (OR = 1.83; 95%CI 0.90-3.71; p = 0.10), while GSTT1-null (OR = 2.42; 95%CI 1.17-5.02; p= 0.01) was associated with increased breast cancer risk. The GSTM1/GSTT1 double null was not associated with an increased risk of developing breast cancer (OR = 2.52; 95%CI 0.75-8.45; p = 0.20). Furthermore, analysis found no association between GSTM1-null (OR =1.12; 95%CI 0.08-15.50; p = 1.00) or GSTT1-null (OR = 1.71; 95%CI 0.13-22.51; p = 1.00) and the disease stage of familial breast cancer patients or sporadic breast cancer patients (GSTM1 (OR = 0.40; 95%CI 0.12-1.32; p = 0.20) and GSTT1 (OR = 1.41; 95%CI 0.39-5.12; p = 0.75)). Also, body mass index (BMI) was not associated with increased or decreased breast cancer risk in either GSTM1-null (OR = 0.60; 95%CI 0.21-1.68; p = 0.44) or GSTT1-null (OR = 0.60; 95%CI 0.21-1.68; p =0.45). Conclusion Our results suggest that only GSTT1-null is associated with increased susceptibility to breast cancer development.
AbstractList Background and objective Breast cancer remains the most common cause of cancer mortality in women. The aim of this study was to investigate associations between genetic variability in GSTM1 and GSTT1 and susceptibility to breast cancer. Methods Genomic DNA was extracted from blood samples for 80 cases of histologically diagnosed breast cancer and 100 control subjects. Genotyping analyses were performed by PCR-based methods. Associations between specific genotypes and the development of breast cancer were examined using logistic regression to calculate odds ratios [1] and 95% confidence intervals (95%CI). Results No correlation was found between GSTM1-null and breast cancer (OR = 1.83; 95%CI 0.90-3.71; p = 0.10), while GSTT1-null (OR = 2.42; 95%CI 1.17-5.02; p= 0.01) was associated with increased breast cancer risk. The GSTM1/GSTT1 double null was not associated with an increased risk of developing breast cancer (OR = 2.52; 95%CI 0.75-8.45; p = 0.20). Furthermore, analysis found no association between GSTM1-null (OR =1.12; 95%CI 0.08-15.50; p = 1.00) or GSTT1-null (OR = 1.71; 95%CI 0.13-22.51; p = 1.00) and the disease stage of familial breast cancer patients or sporadic breast cancer patients (GSTM1 (OR = 0.40; 95%CI 0.12-1.32; p = 0.20) and GSTT1 (OR = 1.41; 95%CI 0.39-5.12; p = 0.75)). Also, body mass index (BMI) was not associated with increased or decreased breast cancer risk in either GSTM1-null (OR = 0.60; 95%CI 0.21-1.68; p = 0.44) or GSTT1-null (OR = 0.60; 95%CI 0.21-1.68; p =0.45). Conclusion Our results suggest that only GSTT1-null is associated with increased susceptibility to breast cancer development.
Author Kiendrebeogo, Isabelle Touwendpoulimdé
Zoure, Abdou Azaque
Yelemkoure, Edwige T
Simpore, Jacques
Bakri, Youssef
Tovo, Sessi Frida
Sawadogo, Alexis Yobi
Bambara, Aboubacar Hierrhum
Sombie, Herman Karim
Ouattara, Abdoul Karim
Sorgho, Pegdwendé Abel
Yonli, Albert Théophane
Djigma, Florencia Wendkuuni
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  givenname: Isabelle Touwendpoulimdé
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  fullname: Kiendrebeogo, Isabelle Touwendpoulimdé
  organization: Pietro Annigoni Biomolecular Research Center (CERBA), 01 P.O. Box 364, Ouagadougou 01, Ouagadougou, Burkina Faso
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  givenname: Abdou Azaque
  surname: Zoure
  fullname: Zoure, Abdou Azaque
  organization: Institute of Health Sciences Research, (IRSS/CNRST)/ Department of Biomedical and Public Health, 03 BP 7192 Ouagadougou 03, Ouagadougou Burkina Faso
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  givenname: Pegdwendé Abel
  surname: Sorgho
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  organization: Pietro Annigoni Biomolecular Research Center (CERBA), 01 P.O. Box 364, Ouagadougou 01, Ouagadougou, Burkina Faso
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  givenname: Albert Théophane
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  givenname: Florencia Wendkuuni
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  givenname: Abdoul Karim
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  organization: Pietro Annigoni Biomolecular Research Center (CERBA), 01 P.O. Box 364, Ouagadougou 01, Ouagadougou, Burkina Faso
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  givenname: Herman Karim
  surname: Sombie
  fullname: Sombie, Herman Karim
  organization: Pietro Annigoni Biomolecular Research Center (CERBA), 01 P.O. Box 364, Ouagadougou 01, Ouagadougou, Burkina Faso
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  givenname: Sessi Frida
  surname: Tovo
  fullname: Tovo, Sessi Frida
  organization: Pietro Annigoni Biomolecular Research Center (CERBA), 01 P.O. Box 364, Ouagadougou 01, Ouagadougou, Burkina Faso
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  givenname: Edwige T
  surname: Yelemkoure
  fullname: Yelemkoure, Edwige T
  organization: Pietro Annigoni Biomolecular Research Center (CERBA), 01 P.O. Box 364, Ouagadougou 01, Ouagadougou, Burkina Faso
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  givenname: Aboubacar Hierrhum
  surname: Bambara
  fullname: Bambara, Aboubacar Hierrhum
  organization: Service of oncology, University Hospital Yalgado OUEDRAOGO, University Joseph KI ZERBO, UFR/SDS, Ouagadougou, Burkina Faso
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  givenname: Alexis Yobi
  surname: Sawadogo
  fullname: Sawadogo, Alexis Yobi
  organization: Service of Gynecology, University Hospital Yalgado OUEDRAOGO, University Joseph KI ZERBO, UFR/SDS, Ouagadougou, Burkina Faso
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  givenname: Youssef
  surname: Bakri
  fullname: Bakri, Youssef
  organization: Laboratoire de Biologie des Pathologies Humaines-BioPatH. Faculty of Sciences, University of Mohammed V-Rabat, Rabat, Morocco
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  givenname: Jacques
  surname: Simpore
  fullname: Simpore, Jacques
  organization: Laboratory of Molecular Biology and Genetics (LABIOGENE), UFR/SVT, University Joseph Ki-Zerbo, 03 P.O. Box 7021, Ouagadougou 03, Ouagadougou, Burkina Faso
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Keywords Breast cancer risk
Burkina Faso
GSTM1-GSTT1
Genotypes
Language English
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Snippet Background and objective Breast cancer remains the most common cause of cancer mortality in women. The aim of this study was to investigate associations...
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StartPage 175
SubjectTerms Adult
Aged
Breast Neoplasms - genetics
Burkina Faso
Female
Glutathione Transferase - genetics
Humans
Loss of Function Mutation
Middle Aged
Polymorphism, Single Nucleotide
Title Glutathione S-transferase M1 (GSTM1) and T1 (GSTT1) variants and breast cancer risk in Burkina Faso
URI https://www.ncbi.nlm.nih.gov/pubmed/31707358
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