Literature DB >> 21311890

RET-protooncogene variants in patients with sporadic neoplasms of the digestive tract and the central nervous system.

Felix Rückert1, Heike Görgens, Ines Richter, Dietmar Krex, Gabriele Schackert, Eberhard Kuhlisch, Guido Fitze, Hans-Detlev Saeger, Christian Pilarsky, Robert Grützmann, Hans K Schackert.   

Abstract

PURPOSE: The RET protooncogene plays a crucial role in neural crest development; accordingly, mutations of RET cause MEN2A and familial medullary thyroid carcinoma, while the expression deregulation of RET is involved in the pathophysiology of glioblastoma multiforme (GBM) and pancreatic cancer (PDAC). The aim of this study was to evaluate if germline variants of the RET protooncogene are associated with GBM, pancreatic cancer and gastric cancer (GC).
METHODS: Genomic DNA from peripheral blood was isolated from 100 patients with GBM, 65 patients with GC and 54 patients with PDAC. The coding sequence of RET promoter, exon 2 and exon 13 was amplified. Sequence variations at -5 and -1 in the promotor and in exon 2 were determined through a LightCycler assay, and analysis of exon 13 was carried out by genomic sequencing.
RESULTS: There was no significant association of the RET-promoter or exon 2 genotypes with the phenotype in the different populations, although there was an increase of the GG genotype of the -5G>A variant in all cancers compared to controls. Sequencing of exon 13 identified mutation c.2372A>T in codon 791 (Y791F) in heterozygous state in one of 100 GBM patients, in two of 65 patients with gastric cancer, in two of 54 PDAC patients and in none of the controls.
CONCLUSIONS: Although our data did not reach significance in our small cohorts, we cannot rule out the involvement of the -5G promoter allele and the c.2372A>T mutation in the development of the aforementioned tumours.

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Year:  2011        PMID: 21311890     DOI: 10.1007/s00384-011-1150-7

Source DB:  PubMed          Journal:  Int J Colorectal Dis        ISSN: 0179-1958            Impact factor:   2.571


  23 in total

1.  Specific polymorphisms in the RET proto-oncogene are over-represented in patients with Hirschsprung disease and may represent loci modifying phenotypic expression.

Authors:  S Borrego; M E Sáez; A Ruiz; O Gimm; M López-Alonso; G Antiñolo; C Eng
Journal:  J Med Genet       Date:  1999-10       Impact factor: 6.318

2.  Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).

Authors:  Guido Fitze; Hella Appelt; Inke R König; Heike Görgens; Ulrike Stein; Wolfgang Walther; Manfred Gossen; Matthias Schreiber; Andreas Ziegler; Dietmar Roesner; Hans K Schackert
Journal:  Hum Mol Genet       Date:  2003-11-04       Impact factor: 6.150

3.  One-step analysis of ten functional haplotype combinations of the basic RET promoter with a LightCycler assay.

Authors:  Heike Görgens; Guido Fitze; Dietmar Roesner; Hans K Schackert
Journal:  Clin Chem       Date:  2004-07-20       Impact factor: 8.327

4.  Various penetrance of familial medullary thyroid carcinoma in patients with RET protooncogene codon 790/791 germline mutations.

Authors:  Guido Fitze; Mandy Schierz; Jan Bredow; Hans D Saeger; Dietmar Roesner; Hans K Schackert
Journal:  Ann Surg       Date:  2002-11       Impact factor: 12.969

5.  Catalytic specificity of protein-tyrosine kinases is critical for selective signalling.

Authors:  Z Songyang; K L Carraway; M J Eck; S C Harrison; R A Feldman; M Mohammadi; J Schlessinger; S R Hubbard; D P Smith; C Eng
Journal:  Nature       Date:  1995-02-09       Impact factor: 49.962

6.  Genomic organisation of the mouse Ret proto-oncogene.

Authors:  D Panetta; L Yin; R Barale; G Romeo; R Ravazzolo; I Ceccherini; A Puliti
Journal:  DNA Seq       Date:  2001

7.  Specific expression of the ret proto-oncogene in human neuroblastoma cell lines.

Authors:  I Ikeda; Y Ishizaka; T Tahira; T Suzuki; M Onda; T Sugimura; M Nagao
Journal:  Oncogene       Date:  1990-09       Impact factor: 9.867

8.  Glial cell line-derived neurotrophic factor (GDNF) and its receptor (GFR-alpha 1) are strongly expressed in human gliomas.

Authors:  B Wiesenhofer; G Stockhammer; H Kostron; H Maier; H Hinterhuber; C Humpel
Journal:  Acta Neuropathol       Date:  2000-02       Impact factor: 17.088

9.  The G691S RET polymorphism increases glial cell line-derived neurotrophic factor-induced pancreatic cancer cell invasion by amplifying mitogen-activated protein kinase signaling.

Authors:  Hirozumi Sawai; Yuji Okada; Kevork Kazanjian; Joseph Kim; Sascha Hasan; Oscar J Hines; Howard A Reber; Dave S B Hoon; Guido Eibl
Journal:  Cancer Res       Date:  2005-12-15       Impact factor: 12.701

10.  A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A.

Authors:  I Berndt; M Reuter; B Saller; K Frank-Raue; P Groth; M Grussendorf; F Raue; M M Ritter; W Höppner
Journal:  J Clin Endocrinol Metab       Date:  1998-03       Impact factor: 5.958

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  3 in total

1.  Prevalence by age and predictors of medullary thyroid cancer in patients with lower risk germline RET proto-oncogene mutations.

Authors:  Thereasa A Rich; Lei Feng; Naifa Busaidy; Gilbert J Cote; Robert F Gagel; Mimi Hu; Camilo Jimenez; Jeffrey E Lee; Nancy Perrier; Steven I Sherman; Steven G Waguespack; Anita Ying; Elizabeth Grubbs
Journal:  Thyroid       Date:  2014-06-06       Impact factor: 6.568

2.  Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility.

Authors:  Rodrigo A Toledo; Roxanne Hatakana; Delmar M Lourenço; Susan C Lindsey; Cleber P Camacho; Marcio Almeida; José V Lima; Tomoko Sekiya; Elena Garralda; Michel S Naslavsky; Guilherme L Yamamoto; Monize Lazar; Osorio Meirelles; Tiago J P Sobreira; Maria Lucia Lebrao; Yeda A O Duarte; John Blangero; Mayana Zatz; Janete M Cerutti; Rui M B Maciel; Sergio P A Toledo
Journal:  Endocr Relat Cancer       Date:  2014-11-25       Impact factor: 5.678

3.  Distribution of RET proto-oncogene variants in children with appendicitis.

Authors:  Jurek Schultz; Ines Freibothe; Michael Haase; Patrick Glatte; Gustavo Barreton; Andreas Ziegler; Heike Görgens; Guido Fitze
Journal:  Mol Genet Genomic Med       Date:  2022-01-03       Impact factor: 2.473

  3 in total

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