|
Specific TaqMan allelic discrimination assay for rs1477196 and rs9939609 single nucleotide polymorphisms of FTO gene demonstrated that there is no association between these SNPs and risk of breast cancer in Iranian women
Mahboobeh Mojaver1, Fariborz Mokarian2, Mohammad Kazemi1, Mansoor Salehi3
1 Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, and Medical Genetics Center of Genome, Shariati St., Isfahan, Iran
2 Department of Clinical Oncology, Medical School, Isfahan University of Medical Sciences, Isfahan, and Medical Genetics Center of Genome, Shariati St., Isfahan, Iran
3 Department of Medical Genetics, Medical School, Isfahan University of Medical Sciences, Isfahan, and Medical Genetics Center of Genome, Shariati St., Isfahan, Iran
| Date of Submission | 21-Jun-2013 |
| Date of Acceptance | 20-Jan-2014 |
| Date of Web Publication | 27-Jul-2015 |
Correspondence Address:
Mansoor Salehi
Department of Genetics and Molecular Biology, Medical School, Isfahan University of Medical Sciences, Hezar Jarib Street, Isfahan
Iran
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/2277-9175.161532
Background: Breast cancer (BC), is the most common cancer in women, that is the major cause of cancer-related morbidity and mortality in women. Obesity is considered as a major risk factor for BC that increases both the rate and intensity of the disease. Polymorphisms in FTO gene, a known obesity related gene, is shown to be associated with obesity-related traits as well. The aim of this study was to evaluate the association between previously reported single nucleotide polymorphisms (SNPs) of intron 1of FTO gene, rs1477196 and rs9939609 and risk of BC in a subset of Iranian BC patients.
Materials and Methods: We genotyped 99 cases and 100 controls for the two SNPs of rs9939609 and rs1477196 by TaqMan allelic discrimination assay. For each sample in an allelic discrimination assay, a unique pair of fluorescent dye probe is used. One fluorescent dye probe has a perfect match with the wild type allele and the other fluorescent dye probe is perfectly matched to the mutated allele.
Results: Our research has shown that the observed differences between case and control groups in the studied SNPs of FTO gene are not statistically significant (P > 0.05).
Conclusions: Our findings suggest that there is no association between rs9939609 and rs1477196 polymorphisms in FTO gene and increase in risk of BC in the studied Iranian population. These results were inconsistent with that of previously reported case-control studies with BC that means presence of these polymorphisms depends on ethnic group. Keywords: Breast cancer, FTO gene, polymorphism
How to cite this article:
Mojaver M, Mokarian F, Kazemi M, Salehi M. Specific TaqMan allelic discrimination assay for rs1477196 and rs9939609 single nucleotide polymorphisms of FTO gene demonstrated that there is no association between these SNPs and risk of breast cancer in Iranian women. Adv Biomed Res 2015;4:136 |
How to cite this URL:
Mojaver M, Mokarian F, Kazemi M, Salehi M. Specific TaqMan allelic discrimination assay for rs1477196 and rs9939609 single nucleotide polymorphisms of FTO gene demonstrated that there is no association between these SNPs and risk of breast cancer in Iranian women. Adv Biomed Res [serial online] 2015 [cited 2023 May 30];4:136. Available from: https://www.advbiores.net/text.asp?2015/4/1/136/161532 |
| Introduction | |  |
Cancer is one of the most serious global health crisis which causes one out of every four deaths in the USA. [1] Several studies revealed that breast cancer (BC) comprises 29% (226,870 patients) of new cases of diagnosed cancers among women of US in 2012, so it is one of the most frequently diagnosed cancers in women. [1] Based on the Iranian cancer registry database, incidence of BC in Iran has been growing in the past two decades. [2] In Iran, incidence of BC is 24.4% of all cancer cases that is considered as a relatively high incidence [2],[3] also, the patients are diagnosed in advanced stages of the disease. Interestingly the age of onset of BC in Iran is about 10 years younger than the patients in developed countries. [4],[5] The alarming rises in the prevalence of obesity worldwide in the last three decades to its epidemic level, has augmented obesity related co-morbidities such as diabetes, cardiovascular diseases and particularly cancer. [6],[7],[8] Epidemiological studies of cancer, have shown that in several cancers such as kidney, breast, colon and gallbladder, obesity contributes to the increased incidence and death from cancers as much as 3 times higher. [6],[8],[9] Genome-wide association studies demonstrated that there are some obesity-associated single nucleotide polymorphisms (SNPs) in the intron 1 of the fat mass and obesity associated (FTO) gene which is reproducibly shown to be associated with body mass index (BMI) and other obesity-related traits in different ethnic groups. [10],[11]
Although the exact cellular and physiological function of FTO is ambiguous but based on bioinformatics analyses, FTO double-stranded b-helix fold protein structure has homology with Fe (II)- and 2-oxoglutarate (2OG) -dependent oxygenases. [8],[12],[13],[14] These enzymes uses non-heme iron as a co-factor and 2OG as a co-substrate and oxidatesa mixture of substrates. [7] Gerken et al. verified that the 2OG-dependent nucleic acid demethylase encoded by FTO gene, in vitro, removes methyl group from 3-methylthymine and repair deoxyribonucleic acid (DNA) methylation damage by hydroxylating methyl groups on the DNA, in particular single-stranded DNA. [12],[13],[14],[15],[16],[17]
A number of studies have revealed that this gene is highly conserved not only in human, vertebrate and other animals but also even in algae. Although this gene is expressed in different tissues but has the highest expression in the hypothalamic arcuate nucleus, one of the main appetite regulating centers. [10]
Given the association between obesity and BC is approved, we performed a case control study to evaluate the association between two SNPs in intron1of FTO gene, the region most associated with obesity. Former studies demonstrated that there is controversy about the association of these SNPs with BC. [14],[18]
There are several SNP genotyping methods, which can be divided into 4 classes: Hybridization-based methods, polymerase chain reaction (PCR)-based methods, restriction site cleavage methods and mixed methods. [19] Between these methods, real time PCR, due to its actual time detection and specially TaqMan genotyping method because of its accuracy and speed and also because it is less sensitive to the quality and concentration of the DNA is considered as one of the best methods. [20] In this method, probes are designed for each sequence variation, makes this a very specific method which produces more reliable and robust results.
| Materials and methods | | |
Study participants
The study was approved by the ethics committee of the Isfahan University of Medical Science. Our case-control study included 99 cases of BC patients and 100 controls from Isfahan province between 2012 and 2013. Only, 62 of the case and controls answered to our questionnaires, but we used both of this population in our studies. Prospective participants were recommended by physicians and the samples were obtained from recruited patients referred to the Omid Hospital, Isfahan, Iran. The controls were selected from apparently healthy people. Cases and controls were matched for sex, age, BMI and all of the participants were of the same ethnicity. Blood samples were obtained from the case and control individuals after obtaining signed informed consent.
DNA extraction
The whole blood Genet Bio DNA Blood Kit was used to extract DNA from 200 μl of blood lymphocytes and extracted DNAs were stored at −20°C until used for genotyping.
SNP genotyping
Two SNPs, rs1477196 and rs9939609 of FTO gene selected for evaluation. Based on previous data, these SNPs which are located in intron 1 of FTO gene, are strongly associated with obesity. All PCRs were prepared in a volume of 10 μl, containing TaqMan Universal PCR Master Mix, specific TaqMan SNP Genotyping Assays (Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 99404, USA) and genomic DNA. Thermal cycling conditions were 10 min at 95°C, followed by 40 cycles of 92°C for 15 s and 60°C for 1 min. Genotyping of both rs1477196and rs9939609 SNPs, was performed by 5΄ nuclease PCR using the TaqMan allelic discrimination system. All results were automatically called by step one software version 2.2. The quality value for all genotype calls (with a 95% certainty) was calculated.
Statistical analysis
Statistical analyses were carried out using SPSS software, version 20. t-test was first used to compare the mean of age, weight, height and BMI between cases and controls. Genotype frequencies for individual markers were compared in patients and control subjects using Chi-square test. We used logistic regression models to analyze our data simultaneously on each SNP. We first performed our analyses without any co-variates, and then adjusted for age, BMI and menopause status by including them as co-variates.
The odds ratios (OR) was estimated with 95% confidence intervals (95% CI) and P < 0.05 was considered statistically significant.
| Results | | |
Demographic profile
Demographic properties of the cases and controls are shown in [Table 1]. Our case control study included 62 cases and 62 controls. Mean age of the patient and control subjects were 50 years (50.16 ± 11.30) and 49 years (49.63 ± 11.88) respectively. Variance of weight, height and BMI in the case and controls were checked to be insignificant (P = 0.863, 0.097, 0.863 respectively). Hence, the matching on these variables were adequate [Table 1]. | Table 1: Demographic characteristics of breast cancer patients and normal controls
Click here to view |
rs9939609 polymorphism in BC
The genotype of rs9939609 polymorphism in all patients and controls were successfully genotyped. The genotyping by TaqMan genotyping assay was confirmed by sequence analysis of PCR products. The frequency of allelic and genotype distribution of rs9939609 in the case and control subjects is shown in [Table 2]. The frequencies of the T/T, A/T, and A/A genotypes of rs9939609 T > A were 32%, 52% and 16% in controls and 42%, 40% and 11% of cases, respectively. Frequency of the A allele in cases (38%) and healthy control group (42%) were not statistically significant (P = 0.516.). Therefore, no association was observed between the genotype TT and the T allele of rs6983267 T > A SNP and higher BC risk. | Table 2: Allele and genotype characteristics of rs9939609 and rs1477196 in cases and controls
Click here to view |
rs1477196 polymorphism in BC
TaqMan geno typing of rs1477196 polymorphism in patients and controls showed that the frequency of A/A, A/G, G/G genotypes of rs1477196 were 53%, 40%, 6%, in cases and 60%, 32%, 8% in control, respectively [Table 2]. Frequencies of A and G alleles were 78% and 22% in controls and 73% and 27% of cases, respectively. These data indicate that there are no statistically differences in the genotype distributions (P > 0.05 or P = 0. 639) and allele frequencies (P = 0.661) of the rs1477196 between the cases and controls.
We evaluated the association between the genotypes of rs1477196 and rs9939609with menopausal status (pre and post menopause). For both the studied polymorphisms the observed differences between pre and post-menopausal status were not statistically significance (P = 0. 052 for cases, and P = 0. 083 for controls). Association between the polymorphism and individual's menopause status for rs9939609, also was investigated. The observed differences between the pre and post-menopausal women with BC were not statistically significant in the case group (P = 0. 793) and in healthy individuals (P = 0. 543).
When taking into account age, BMI and menopause status [Table 3], the estimated ORs indicated that although menopause status has the highest effect (OR = 1. 892, 95% CI: 0.488-7.343), but none of these quantities are statistically significant. | Table 3: Results of association between breast cancer and studied variables in multiple logistic regression model
Click here to view |
When the association of rs9939609 and rs1477196 with BC were studied in 99 patients and 100 control subjects, that were not matched, our results indicated that there was not any association between these SNPs and risk of BC in Iranian women (P = 0. 389 for rs1477196 and P = 0. 385 for rs9939609).
| Discussion | | |
SNPs as the simplest and most common source of human genetic polymorphisms, which causes individual differences in susceptibility to the disease, may influence the susceptibility to cancer. Several studies have shown that some polymorphisms in non-coding areas, such as intron, may be located in the regulatory sequence of the gene and may affect the expression and function of proteins and have an association with the cancer risk. A study conducted in 2010 by Berulava and Horsthemke clearly showed that the FTO transcripts containing risk allele (A) of rs9939609, are abundant compare to the transcript containing T allele. Transcript high levels may be associated with high levels of the protein product. [11] Obesity is an important risk factor for BC that increases 3-fold (OR = 3.21) BC risk in obese Iranian women, compared with women with normal BMI. [21] It is shown that obesity related hormones such as Adiponectin and Adipokine, have a role in BC risk. [22],[23] Given that, influence of stated SNPs on obesity development are well-assessed and the association of these SNPs with BC, has been demonstrated by Kaklamani et al. [14] we evaluated the association between BC and two FTO polymorphisms among Iranian patients. In our study, one of the evaluated polymorphisms that its effect on risk of BC was investigated, was rs9939609 SNP on chromosome16 q22.2:53800954. A study carried out by Kaklamani et al. in the USA, is shown that this polymorphism has significant association with increased risk of BC. It is reported that individuals carrying the A allele have a higher risk of developing BC [14] . Interestingly, in another study conducted in the Netherlands by Renata Kusinska, Allele A of rs9939609 showed no association with increased risk of developing BC. [18] We carried out this study to evaluate the correlation between this polymorphism and BC in Iranians. [Table 2] shows the results of allele and genotype related to rs9939609 SNP for BC susceptibility. Our findings are not consistent with those of a previous study in the USA population which showed that individuals carrying the A allele have a significantly higher risk of developing BC.
For the other SNP, the rs1477196 SNPs, genotype distribution and allele frequency between the control and case groups were not statistically different. In this study, no association was detected between G allele and GG genotype with BC. Only, in a study conducted by Kaklamani et al., association of rs1477196 with BC was examined Their results demonstrated that rs1477196 SNP showed the strongest association with BC, compared with other SNPs located in intron 1 of the FTO gene. [14]
Studies conducted on the association of obesity with risk of BC in Western women, have shown conflicting results. Studies on postmenopausal women, has demonstrated that there are association between obesity and BC risk, whereas this relationship between pre-menopausal women, is negative. In our study, although there was a link between the high BMI and menopausal status and hence that postmenopausal individuals had high BMI. However when participants were divided into two groups according to their menopause status; and rs9939609, rs1477196 with their menopausal status was examined, the results indicated that the allelic frequency and genotype distributions of these two SNPs, in menopause and non-menopause healthy and patient women did not show any significant difference.
When patients and controls were stratified on the basis of age, BMI and menopausal status, no association was found between these variables and genotype distribution. These findings suggest that both SNPs studied in this survey, rs9939609 and rs1477196 might work in an ethnic-specific mode rather than in a general mode.
Due to the different genetic background of the populations, the study of different polymorphisms in different parts of the world can have different results. For example, allele frequency of the risk factor (A) of rs1477196 in Asia, Europe, Africa and America, are 26%, 35%, 44% and 8% respectively. [24] Unfortunately, the allele frequencies of these polymorphisms in Iran, is not known.
The differences in ethnic background and the different forms of BC may somehow explain the contradictory observed in different studies. These conflicting results may be due to limitations in the assessment of phenotypes, racial differences in genotype frequency of FTO gene, uncontrolled interfering factors in some studies, and differences in demographic and environmental risk factors for BC.
Overall, results of this study indicate that SNPs in the FTO gene, has no role in BC risk in Iranian population.
Our study further demonstrated that the role of adipose tissue in the development of cancer is very complicated and the role of the individual's genetic background polymorphisms in this pathway, has remained more elusive. In order to clarify the role of SNPs on this route, which may play a role in carcinogenesis, we require further studies in different populations, as well as considering the influence of environmental factors.
| Acknowledgments | | |
The author would like to thank Isfahan University of Medical Science for their support. We also, gratefully thank the sincerely collaboration of the stuff of Omid and Alzahra hospital, in collecting samples.
| References | | |
| 1. | Siegel R, Naishadham D, Jemal A. Cancer statistics, 2012. CA Cancer J Clin 2012;62:10-29.  |
| 2. | Hajian-Tilaki KO, Gholizadehpasha AR, Bozorgzadeh S, Hajian-Tilaki E. Body mass index and waist circumference are predictor biomarkers of breast cancer risk in Iranian women. Med Oncol 2011;28:1296-301. |
| 3. | Harirchi I, Kolahdoozan S, Karbakhsh M, Chegini N, Mohseni SM, Montazeri A, et al. Twenty years of breast cancer in Iran: Downstaging without a formal screening program. Ann Oncol 2011;22:93-7. |
| 4. | Mousavi SM, Montazeri A, Mohagheghi MA, Jarrahi AM, Harirchi I, Najafi M, et al. Breast cancer in Iran: An epidemiological review. Breast J 2007;13:383-91. |
| 5. | Taghavi A, Fazeli Z, Vahedi M, Baghestani AR, Pourhoseingholi A, Barzegar F, et al. Increased trend of breast cancer mortality in Iran. Asian Pac J Cancer Prev 2012;13:367-70. |
| 6. | Brennan P, McKay J, Moore L, Zaridze D, Mukeria A, Szeszenia-Dabrowska N, et al. Obesity and cancer: Mendelian randomization approach utilizing the FTO genotype. Int J Epidemiol 2009;38:971-5. |
| 7. | Fawcett KA, Barroso I. The genetics of obesity: FTO leads the way. Trends Genet 2010;26:266-74. |
| 8. | Wu Q, Saunders RA, Szkudlarek-Mikho M, Serna Ide L, Chin KV. The obesity-associated Fto gene is a transcriptional coactivator. Biochem Biophys Res Commun 2010;401:390-5. |
| 9. | Calle EE, Kaaks R. Overweight, obesity and cancer: Epidemiological evidence and proposed mechanisms. Nat Rev Cancer 2004;4:579-91. |
| 10. | Sébert SP, Hyatt MA, Chan LL, Yiallourides M, Fainberg HP, Patel N, et al. Influence of prenatal nutrition and obesity on tissue specific fat mass and obesity-associated (FTO) gene expression. Reproduction 2010;139:265-74. |
| 11. | Berulava T, Horsthemke B. The obesity-associated SNPs in intron 1 of the FTO gene affect primary transcript levels. Eur J Hum Genet 2010;18:1054-6. |
| 12. | Gao X, Shin YH, Li M, Wang F, Tong Q, Zhang P. The fat mass and obesity associated gene FTO functions in the brain to regulate postnatal growth in mice. PLoS One 2010;5:e14005. |
| 13. | Ingman C. Fat mass and obesity associated (FTO) gene involvement in food intake regulation. Uppsala University; 2010. |
| 14. | Kaklamani V, Yi N, Sadim M, Siziopikou K, Zhang K, Xu Y, et al. The role of the fat mass and obesity associated gene (FTO) in breast cancer risk. BMC Med Genet 2011;12:52. |
| 15. | Almén MS, Jacobsson JA, Moschonis G, Benedict C, Chrousos GP, Fredriksson R, et al. Genome wide analysis reveals association of a FTO gene variant with epigenetic changes. Genomics 2012;99:132-7. |
| 16. | Jia G, Yang CG, Yang S, Jian X, Yi C, Zhou Z, et al. Oxidative demethylation of 3-methylthymine and 3-methyluracil in single-stranded DNA and RNA by mouse and human FTO. FEBS Lett 2008;582:3313-9. |
| 17. | Gerken T, Girard CA, Tung Y-CL, Webby1 CJ, Saudek V, Hewitson KS, et al. The Obesity-Associated FTO Gene Encodes a 2-Oxoglutarate-Dependent Nucleic Acid Demethylase. Science. 2007;30:1469-72. |
| 18. | Kusinska R, Górniak P, Pastorczak A, Fendler W, Potemski P, Mlynarski W, et al. Influence of genomic variation in FTO at 16q12.2, MC4R at 18q22 and NRXN3 at 14q31 genes on breast cancer risk. Mol Biol Rep 2012;39:2915-9. |
| 19. | Angaji SA, Akashi K, Darvishani S, Azad MS SNP and its applications in treating human diseases. Aust J Basic Appl Sci 2011;5:424-32. |
| 20. | Eckerman M. Comparison between probe-based TaqMan and HRM detection for SNP analysis considering genotyping of APOE honours. Thesis in Biomedicine, Advanced Level 30 ECTS. School of Life Sciences Skövde University BOX 408 SE-541 28 Skövde Sweden. |
| 21. | Montazeri A, Sadighi J, Farzadi F, Maftoon F, Vahdaninia M, Ansari M, et al. Weight, height, body mass index and risk of breast cancer in postmenopausal women: A case-control study. BMC Cancer 2008;8:278. |
| 22. | Rahmati-Yamchi M, Zarghami N, Rahbani M, Montazeri A. Plasma leptin, hTERT gene expression, and anthropometric measures in obese and non-obese women with breast cancer. Breast Cancer (Auckl) 2011;5:27-35. |
| 23. | Jardé T, Caldefie-Chézet F, Goncalves-Mendes N, Mishellany F, Buechler C, Penault-Llorca F, et al. Involvement of adiponectin and leptin in breast cancer: Clinical and in vitro studies. Endocr Relat Cancer 2009;16:1197-210. |
| 24. | Available from: http://www.asia.ensembl.org/Homo_sapiens/Variation/Population?db=core;r=16:53807758-53808758;v=rs1477196;vdb=variation;vf=1139083. [Last accessed on 2013 jun 20]. |
[Table 1], [Table 2], [Table 3]
| This article has been cited by | | 1 |
Association of fat mass and obesity-associated (FTO) gene polymorphisms with non-communicable diseases (NCDs) in the Iranian population: A systematic review of observational studies |
|
| Zahra Hoseini Tavassol, Seyed Mohammad Mousavi, Bahareh Molaei, Fatemeh Bandarian, Hanieh-Sadat Ejtahed, Kazem Khalagi, Shima Ghannadi, Bagher Larijani, Shirin Hasani-Ranjbar | | Journal of Diabetes & Metabolic Disorders. 2022; | | [Pubmed] | [DOI] | | | 2 |
The Role of FTO in Tumors and Its Research Progress |
|
| Hao Wei, Zhen Li , Fang Liu, Yang Wang, Shi Ding, Ye Chen , Ju Liu | | Current Medicinal Chemistry. 2022; 29(5): 924 | | [Pubmed] | [DOI] | | | 3 |
Development of a TaqMan® Allelic Discrimination qPCR Assay for Rapid Detection of Equine CXCL16 Allelic Variants Associated With the Establishment of Long-Term Equine Arteritis Virus Carrier State in Stallions |
|
| Come J. Thieulent, Mariano Carossino, Udeni B. R. Balasuriya, Kathryn Graves, Ernest Bailey, John Eberth, Igor F. Canisso, Frank M. Andrews, Michael L. Keowen, Yun Young Go | | Frontiers in Genetics. 2022; 13 | | [Pubmed] | [DOI] | | | 4 |
FTO Gene Polymorphisms Contribute to the Predisposition and Radiotherapy Efficiency of Nasopharyngeal Carcinoma |
|
| Feng Xiao,Jianrong Zhou | | Pharmacogenomics and Personalized Medicine. 2021; Volume 14: 1239 | | [Pubmed] | [DOI] | | | 5 |
Interactions of anthropometric indices, rs9939609 FTO gene polymorphism and breast cancer: A case-control study |
|
| Saeid Doaei,Fatemeh Bourbour,Samira Rastgoo,Mohammad Esmail Akbari,Maryam Gholamalizadeh,Azadeh Hajipour,Alireza Moslem,Fereshteh Ghorat,Mostafa Badeli,Seyedeh Elaheh Bagheri,Atieh Alizadeh,Zohreh Mokhtari,Samaneh Pishdad,Sepehr JavadiKooshesh,Ghasem Azizi Tabesh,Fateme Montazeri,Parvin Joola,Shahla Rezaei,Masoomeh Dorosti,Seyed Alireza Mosavi Jarrahi | | Journal of Cellular and Molecular Medicine. 2021; | | [Pubmed] | [DOI] | | | 6 |
The association between fat mass and obesity-associated (
FTO
) genotype and serum vitamin D level in breast cancer patients |
|
| Maryam Gholamalizadeh,Zohreh Mokhtari,Saeid Doaei,Vahideh Jalili,Sayed Hossein Davoodi,Mona Jonoush,Mohammad Esmail Akbari,Azadeh Hajipour,Bojlul Bahar,Ghasem Azizi Tabesh,Saeed Omidi,Seyed Alireza Mosavi Jarrahi | | Journal of Cellular and Molecular Medicine. 2021; | | [Pubmed] | [DOI] | | | 7 |
Emerging roles of N6-methyladenosine (m6A) modification in breast cancer |
|
| Yanyan Wang,Yujie Zhang,Yushen Du,Meiqi Zhou,Yue Hu,Suzhan Zhang | | Cell & Bioscience. 2020; 10(1) | | [Pubmed] | [DOI] | | | 8 |
The association between FTO rs9939609 gene polymorphism and anthropometric indices in adults |
|
| Mahsa Mehrdad,Majid Fardaei,Mohammad Fararouei,Mohammad Hassan Eftekhari | | Journal of Physiological Anthropology. 2020; 39(1) | | [Pubmed] | [DOI] | | | 9 |
Association between FTO gene polymorphisms and breast cancer: the role of estrogen |
|
| Maryam Gholamalizadeh,Alireza Mosavi Jarrahi,Mohammad Esmail Akbari,Fatemeh Bourbour,Zohreh Mokhtari,Sara Salahshoornezhad,Saeid Doaei | | Expert Review of Endocrinology & Metabolism. 2020; : 1 | | [Pubmed] | [DOI] | | | 10 |
Novel positioning from obesity to cancer: FTO, an m6A RNA demethylase, regulates tumour progression |
|
| JiaLing Chen,Bin Du | | Journal of Cancer Research and Clinical Oncology. 2018; | | [Pubmed] | [DOI] | | | 11 |
Is FTO gene variant related to cancer risk independently of adiposity? An updated meta-analysis of 129,467 cases and 290,633 controls |
|
| Yu Kang,Fang Liu,Yao Liu | | Oncotarget. 2017; 8(31): 50987 | | [Pubmed] | [DOI] | | | 12 |
Association of the hypermethylation status of PTEN tumor suppressor gene with the risk of breast cancer among Kurdish population from Western Iran |
|
| Kheirollah Yari,Mehrdad Payandeh,Zohreh Rahimi | | Tumor Biology. 2015; | | [Pubmed] | [DOI] | |
|
 |
|
|
|
Search Pubmed for