Literature DB >> 27541142

A family-based study of gene variants and maternal folate and choline in neuroblastoma: a report from the Children's Oncology Group.

Angela L Mazul1, Anna Maria Siega-Riz2,3, Clarice R Weinberg4, Stephanie M Engel2, Fei Zou5, Kathryn S Carrier2, Patricia V Basta2,6, Zalman Vaksman7,8, John M Maris7,9, Sharon J Diskin7,9, Charlene Maxen10, Arlene Naranjo11, Andrew F Olshan2.   

Abstract

PURPOSE: Neuroblastoma is a childhood cancer of the sympathetic nervous system with embryonic origins. Previous epidemiologic studies suggest maternal vitamin supplementation during pregnancy reduces the risk of neuroblastoma. We hypothesized offspring and maternal genetic variants in folate-related and choline-related genes are associated with neuroblastoma and modify the effects of maternal intake of folate, choline, and folic acid.
METHODS: The Neuroblastoma Epidemiology in North America (NENA) study recruited 563 affected children and their parents through the Children's Oncology Group's Childhood Cancer Research Network. We used questionnaires to ascertain pre-pregnancy supplementation and estimate usual maternal dietary intake of folate, choline, and folic acid. We genotyped 955 genetic variants related to folate or choline using DNA extracted from saliva samples and used a log-linear model to estimate both child and maternal risk ratios and stratum-specific risk ratios for gene-environment interactions.
RESULTS: Overall, no maternal or offspring genotypic results met criteria for a false discovery rate (FDR) Q-value <0.2. Associations were also null for gene-environment interaction with pre-pregnancy vitamin supplementation, dietary folic acid, and folate. FDR-significant gene-choline interactions were found for offspring SNPs rs10489810 and rs9966612 located in MTHFD1L and TYMS, respectively, with maternal choline dietary intake dichotomized at the first quartile.
CONCLUSION: These results suggest that variants related to one-carbon metabolism are not strongly associated with neuroblastoma. Choline-related variants may play a role; however, the functional consequences of the interacting variants are unknown and require independent replication.

Entities:  

Keywords:  Case–parent triad; Choline; Folate; Genetics; Neuroblastoma

Mesh:

Substances:

Year:  2016        PMID: 27541142      PMCID: PMC5025391          DOI: 10.1007/s10552-016-0799-1

Source DB:  PubMed          Journal:  Cancer Causes Control        ISSN: 0957-5243            Impact factor:   2.506


  42 in total

1.  SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap.

Authors:  Andrew D Johnson; Robert E Handsaker; Sara L Pulit; Marcia M Nizzari; Christopher J O'Donnell; Paul I W de Bakker
Journal:  Bioinformatics       Date:  2008-10-30       Impact factor: 6.937

2.  A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting.

Authors:  C R Weinberg; A J Wilcox; R T Lie
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

3.  Neuroblastoma incidence and survival in European children (1978-1997): report from the Automated Childhood Cancer Information System project.

Authors:  Claudia Spix; Guido Pastore; Risto Sankila; Charles A Stiller; Eva Steliarova-Foucher
Journal:  Eur J Cancer       Date:  2006-09       Impact factor: 9.162

4.  RFC-1 80G>A polymorphism in case-mother/control-mother dyads is associated with risk of nephroblastoma and neuroblastoma.

Authors:  Rafaela Montalvão-de-Azevedo; Gisele M Vasconcelos; Fernando R Vargas; Luiz Claudio Thuler; Maria S Pombo-de-Oliveira; Beatriz de Camargo
Journal:  Genet Test Mol Biomarkers       Date:  2014-12-23

Review 5.  Recent advances in neuroblastoma.

Authors:  John M Maris
Journal:  N Engl J Med       Date:  2010-06-10       Impact factor: 91.245

6.  Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2.

Authors:  Kristen L Deak; Margaret E Dickerson; Elwood Linney; David S Enterline; Timothy M George; Elizabeth C Melvin; Felicia L Graham; Deborah G Siegel; Preston Hammock; Lorraine Mehltretter; Alexander G Bassuk; John A Kessler; John R Gilbert; Marcy C Speer
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2005-11

7.  Reduced folate carrier-1 G80a gene polymorphism is associated with neuroblastoma's development.

Authors:  Dyego O de Miranda; Jemima E X S Barros; Maria Madalena S Vieira; Elker L S Lima; Vera L L Moraes; Helker A da Silva; Helder L B O Garcia; Cássia A Lima; Adriana V Gomes; Neide Santos; Maria T C Muniz
Journal:  Mol Biol Rep       Date:  2014-04-27       Impact factor: 2.316

8.  Gravid health status, medication use, and risk of neuroblastoma.

Authors:  A M Michalek; G M Buck; P C Nasca; A N Freedman; M S Baptiste; M C Mahoney
Journal:  Am J Epidemiol       Date:  1996-05-15       Impact factor: 4.897

9.  Maternal vitamin use and reduced risk of neuroblastoma.

Authors:  Andrew F Olshan; Joanna C Smith; Melissa L Bondy; Joseph P Neglia; Brad H Pollock
Journal:  Epidemiology       Date:  2002-09       Impact factor: 4.822

10.  Common variations in BARD1 influence susceptibility to high-risk neuroblastoma.

Authors:  Mario Capasso; Marcella Devoto; Cuiping Hou; Shahab Asgharzadeh; Joseph T Glessner; Edward F Attiyeh; Yael P Mosse; Cecilia Kim; Sharon J Diskin; Kristina A Cole; Kristopher Bosse; Maura Diamond; Marci Laudenslager; Cynthia Winter; Jonathan P Bradfield; Richard H Scott; Jayanti Jagannathan; Maria Garris; Carmel McConville; Wendy B London; Robert C Seeger; Struan F A Grant; Hongzhe Li; Nazneen Rahman; Eric Rappaport; Hakon Hakonarson; John M Maris
Journal:  Nat Genet       Date:  2009-05-03       Impact factor: 38.330

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  5 in total

1.  Germline 16p11.2 Microdeletion Predisposes to Neuroblastoma.

Authors:  Laura E Egolf; Zalman Vaksman; Gonzalo Lopez; Jo Lynne Rokita; Apexa Modi; Patricia V Basta; Hakon Hakonarson; Andrew F Olshan; Sharon J Diskin
Journal:  Am J Hum Genet       Date:  2019-08-29       Impact factor: 11.025

2.  Neuroblastoma in relation to joint effects of vitamin A and maternal and offspring variants in vitamin A-related genes: A report of the Children's Oncology Group.

Authors:  Angela L Mazul; Clarice R Weinberg; Stephanie M Engel; Anna Maria Siega-Riz; Fei Zou; Kathryn S Carrier; Patricia V Basta; Zalman Vaksman; John M Maris; Sharon J Diskin; Charlene Maxen; Arlene Naranjo; Andrew F Olshan
Journal:  Cancer Epidemiol       Date:  2019-07-04       Impact factor: 2.984

3.  An updated assessment of 43,110 patients enrolled in the Childhood Cancer Research Network: A Children's Oncology Group report.

Authors:  Austin L Brown; Pagna Sok; Michael E Scheurer; Karen R Rabin; Erin L Marcotte; Douglas S Hawkins; Logan G Spector; Philip J Lupo
Journal:  Cancer       Date:  2022-04-28       Impact factor: 6.921

4.  Tumor-suppressive function of SIRT4 in neuroblastoma through mitochondrial damage.

Authors:  Yumei Wang; Yinmou Guo; Jianzhi Gao; Xiangdong Yuan
Journal:  Cancer Manag Res       Date:  2018-11-09       Impact factor: 3.989

5.  Genetic variation of SORBS1 gene is associated with glucose homeostasis and age at onset of diabetes: A SAPPHIRe Cohort Study.

Authors:  Tien-Jyun Chang; Wen-Chang Wang; Chao A Hsiung; Chih-Tsueng He; Ming-Wei Lin; Wayne Huey-Herng Sheu; Yi-Cheng Chang; Tom Quertermous; Yii-Der Ida Chen; Jerome I Rotter; Lee-Ming Chuang
Journal:  Sci Rep       Date:  2018-07-12       Impact factor: 4.379

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