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 9 条
  • [1] Fumarate Hydratase is a Novel Gene for Familial Non-Medullary Thyroid Cancer
    Alzahrani, Ali S.
    Alswailem, Meshael
    Alghamdi, Balgees
    Al-Hindi, Hindi
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2022, 107 (09) : 2539 - 2544
  • [2] Lack of Mutations in POT1 Gene in Selected Families with Familial Non-Medullary Thyroid Cancer
    Orois, Aida
    Badenas, Celia
    Reverter, Jordi L.
    Lopez, Veronica
    Potrony, Miriam
    Mora, Mireia
    Halperin, Irene
    Oriola, Josep
    HORMONES & CANCER, 2020, 11 (02): : 111 - 116
  • [3] Segregation and expression analyses of hyaluronan-binding protein 2 (HABP2): insights from a large series of familial non-medullary thyroid cancers and literature review
    Colombo, Carla
    Muzza, Marina
    Proverbio, Maria Carla
    Ercoli, Giulia
    Perrino, Michela
    Cirello, Valentina
    Vicentini, Leonardo
    Ferrero, Stefano
    Fugazzola, Laura
    CLINICAL ENDOCRINOLOGY, 2017, 86 (06) : 837 - 844
  • [4] The HABP2 G534E Variant Is an Unlikely Cause of Familial Nonmedullary Thyroid Cancer
    Sahasrabudhe, Ruta
    Stultz, Jacob
    Williamson, John
    Lott, Paul
    Estrada, Ana
    Bohorquez, Mabel
    Palles, Claire
    Polanco-Echeverry, Guadalupe
    Jaeger, Emma
    Martin, Lynn
    Magdalena Echeverry, Maria
    Tomlinson, Ian
    Carvajal-Carmona, Luis G.
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2016, 101 (03) : 1098 - 1103
  • [5] Patients with familial non-medullary thyroid cancer have an outcome similar to that of patients with sporadic papillary thyroid tumors
    Pitoia, Fabian
    Cross, Graciela
    Salvai, Maria E.
    Abelleira, Erika
    Niepomniszcze, Hugo
    ARQUIVOS BRASILEIROS DE ENDOCRINOLOGIA E METABOLOGIA, 2011, 55 (03) : 219 - 223
  • [6] Aryl hydrocarbon receptor interacting protein mutations seem not to associate with familial non-medullary thyroid cancer
    Raitila, A.
    Georgitsi, M.
    Bonora, E.
    Vargiolu, M.
    Tuppurainen, K.
    Makinen, M. J.
    Vierimaa, O.
    Salmela, P. I.
    Launonen, V.
    Vahteristo, P.
    Aaltonen, L. A.
    Romeo, G.
    Karhu, A.
    JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2009, 32 (05): : 426 - 429
  • [7] Thyroid Cancer Genetics: Multiple Endocrine Neoplasia Type 2, Non-Medullary Familial Thyroid Cancer, and Familial Syndromes Associated with Thyroid Cancer
    Richards, Melanie L.
    SURGICAL ONCOLOGY CLINICS OF NORTH AMERICA, 2009, 18 (01) : 39 - +
  • [8] Allelic loss of susceptibility loci and the occurrence of BRAF and RAS mutations in patients with familial non-medullary thyroid cancer
    Na, Kuk Young
    Kim, Ra Mi
    Song, Eun-Mi
    Lee, Ji Hyun
    Lee, Jandee
    Soh, Euy-Young
    JOURNAL OF SURGICAL ONCOLOGY, 2012, 105 (01) : 10 - 14
  • [9] Longer Time to Reach Excellent Response to Treatment in Familial Versus Sporadic Non-medullary Thyroid Cancer (NMTC): A Matched Case-Control Study
    Shafiei, Susan
    Sadrolodabaei, Mehrdokht
    Aghaei, Atena
    Ayati, Narjess
    Namdar, Samira Zare
    Hemati, Donya
    Zakavi, Seyed Rasoul
    INTERNATIONAL JOURNAL OF ENDOCRINOLOGY AND METABOLISM, 2021, 19 (02)