HABP2 Gene Mutations Do Not Cause Familial or Sporadic Non-Medullary Thyroid Cancer in a Highly Inbred Middle Eastern Population

被引:27
作者
Alzahrani, Ali S. [1 ,2 ,3 ]
Murugan, Avaniyapuram Kannan [1 ]
Qasem, Ebtesam [1 ]
Al-Hindi, Hindi [4 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Dept Mol Oncol, Riyadh 11211, Saudi Arabia
[2] King Faisal Specialist Hosp & Res Ctr, Dept Med, POB 3354, Riyadh 11211, Saudi Arabia
[3] King Faisal Specialist Hosp & Res Ctr, Res Ctr Jeddah, Riyadh 11211, Saudi Arabia
[4] King Faisal Specialist Hosp & Res Ctr, Dept Pathol & Lab Med, Riyadh 11211, Saudi Arabia
关键词
FIRST-DEGREE RELATIVES; CARCINOMA; PREDISPOSITION; CONSANGUINITY; PREVALENCE; DISEASE;
D O I
10.1089/thy.2015.0537
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Familial non-medullary thyroid cancer (NMTC) occurs either as part of known hereditary syndromes or as a non-syndromic isolated hereditary tumor. Although the genes underlying the syndromic type of NMTC have been identified in most syndromes, no clear underlying gene has been identified in the non-syndromic NMTC. Recently, a c.1601G>A, p.G534E mutation in the HABP2 gene was reported to be the underlying genetic defect in a family with seven members affected by NMTC. The G534E variant has also been reported to occur in about 4.7% of cases of the Thyroid Cancer Genome Atlas (TCGA) database. Objectives: The aim of this study was to explore whether the recent finding of G534E genetic variant can be replicated in a large sample of NMTC, including 11 members of four unrelated families with familial NMTC and 509 cases of sporadic pediatric (63 cases) and adult NMTC (446 cases). Methods: All exons and exon-intron boundaries of HABP2 were screened in 11 members of four families with familial non-syndromic NMTC using DNA isolated from peripheral leucocytes, polymerase chain reaction, and direct sequencing. The G534E variant was also screened for specifically in 229 cases of sporadic NMTC using DNA isolated from peripheral leucocytes and an additional 217 cases of NMTC using DNA isolated from formalin-fixed paraffin-embedded tumor tissues. As a control cohort, 190 healthy individuals without known thyroid disease were also studied for the presence of the G534E variant using DNA isolated from peripheral leucocytes. Results: None of the familial NMTC carried HABP2 mutations. Of 509 sporadic NMTC, only one case (0.2%) harbored the G534E variant. Similarly, only one case (0.5%) of the control group harbored the G534E variant. Conclusion: In this study, HABP2 mutations were not found in familial NMTC, and the G534E variant is not the underlying genetic defect in a large sample of sporadic NMTC from the Middle East.
引用
收藏
页码:667 / 671
页数:5
相关论文
共 25 条
[1]   Integrated Genomic Characterization of Papillary Thyroid Carcinoma [J].
Agrawal, Nishant ;
Akbani, Rehan ;
Aksoy, B. Arman ;
Ally, Adrian ;
Arachchi, Harindra ;
Asa, Sylvia L. ;
Auman, J. Todd ;
Balasundaram, Miruna ;
Balu, Saianand ;
Baylin, Stephen B. ;
Behera, Madhusmita ;
Bernard, Brady ;
Beroukhim, Rameen ;
Bishop, Justin A. ;
Black, Aaron D. ;
Bodenheimer, Tom ;
Boice, Lori ;
Bootwalla, Moiz S. ;
Bowen, Jay ;
Bowlby, Reanne ;
Bristow, Christopher A. ;
Brookens, Robin ;
Brooks, Denise ;
Bryant, Robert ;
Buda, Elizabeth ;
Butterfield, Yaron S. N. ;
Carling, Tobias ;
Carlsen, Rebecca ;
Carter, Scott L. ;
Carty, Sally E. ;
Chan, Timothy A. ;
Chen, Amy Y. ;
Cherniack, Andrew D. ;
Cheung, Dorothy ;
Chin, Lynda ;
Cho, Juok ;
Chu, Andy ;
Chuah, Eric ;
Cibulskis, Kristian ;
Ciriello, Giovanni ;
Clarke, Amanda ;
Clayman, Gary L. ;
Cope, Leslie ;
Copland, John A. ;
Covington, Kyle ;
Danilova, Ludmila ;
Davidsen, Tanja ;
Demchok, John A. ;
DiCara, Daniel ;
Dhalla, Noreen .
CELL, 2014, 159 (03) :676-690
[2]   Comparison of differentiated thyroid cancer in children and adolescents (20years) with young adults [J].
Alzahrani, Ali S. ;
Alkhafaji, Dania ;
Tuli, Mahmoud ;
Al-Hindi, Hindi ;
Bin Sadiq, Bakr .
CLINICAL ENDOCRINOLOGY, 2016, 84 (04) :571-577
[3]   Cancer as a complex phenotype: Pattern of cancer distribution within and beyond the nuclear family [J].
Amundadottir, LT ;
Thorvaldsson, S ;
Gudbjartsson, DF ;
Sulem, P ;
Kristjansson, K ;
Arnason, S ;
Gulcher, JR ;
Bjornsson, J ;
Kong, A ;
Thorsteinsdottir, U ;
Stefansson, K .
PLOS MEDICINE, 2004, 1 (03) :229-236
[4]  
[Anonymous], 2018, ANTI-CANCER DRUG, DOI [DOI 10.3322/caac.20115, DOI 10.1097/CAD.0000000000000617]
[5]   Familial nontoxic multinodular thyroid goiter locus maps to chromosome 149 but does not account for familial nonmedullary thyroid cancer [J].
Bignell, GR ;
Canzian, F ;
Shayeghi, M ;
Stark, M ;
Shugart, YY ;
Biggs, P ;
Mangion, J ;
Hamoudi, R ;
Rosenblatt, J ;
Buu, P ;
Sun, S ;
Stoffer, SS ;
Goldgar, DE ;
Romeo, G ;
Houlston, RS ;
Narod, SA ;
Stratton, MR ;
Foulkes, WD .
AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (05) :1123-1130
[6]   On the prevalence of familial nonmedullary thyroid cancer in multiply affected kindreds [J].
Charkes, ND .
THYROID, 2006, 16 (02) :181-186
[7]  
Ei-Mouzan MI, 2007, SAUDI MED J, V28, P1881
[8]  
Frich L, 2001, CANCER EPIDEM BIOMAR, V10, P113
[9]   Germline HABP2 Mutation Causing Familial Nonmedullary Thyroid Cancer [J].
Gara, Sudheer Kumar ;
Jia, Li ;
Merino, Maria J. ;
Agarwal, Sunita K. ;
Zhang, Lisa ;
Cam, Maggie ;
Patel, Dhaval ;
Kebebew, Electron .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (05) :448-455
[10]   SYSTEMATIC POPULATION-BASED ASSESSMENT OF CANCER RISK IN FIRST-DEGREE RELATIVES OF CANCER PROBANDS [J].
GOLDGAR, DE ;
EASTON, DF ;
CANNONALBRIGHT, LA ;
SKOLNICK, MH .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1994, 86 (21) :1600-1608