Literature DB >> 14669347

Clinical relationship between EDN-3 gene, EDNRB gene and Hirschsprung's disease.

Xiang-Long Duan1, Xian-Sheng Zhang, Guo-Wei Li.   

Abstract

AIM: To investigate the mutation of EDNRB gene and EDN-3 gene in sporadic Hirschsprung's disease (HD) in Chinese population.
METHODS: Genomic DNA was extracted from bowel tissues of 34 unrelated HD patients which were removed by surgery. Exon 3, 4, 6 of EDNRB gene and Exon 1, 2 of EDN-3 gene were amplified by polymerase chain reaction (PCR) and analyzed by single strand conformation polymorphism (SSCP).
RESULTS: EDNRB mutations were detected in 2 of the 13 short-segment HD. One mutant was in the exon 3, the other was in the exon 6. EDN-3 mutation was detected in one of the 13 short-segment HD and in the exon 2. Both EDNRB and EDN-3 mutations were detected in one short-segment HD. No mutations were detected in the ordinary or long-segment HD.
CONCLUSION: The mutations of EDNRB gene and EDN-3 gene are found in the short-segment HD of sporadic Hirschsprung's disease in Chinese population, which suggests that the EDNRB gene and EDN-3 gene play important roles in the pathogenesis of HD.

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Year:  2003        PMID: 14669347      PMCID: PMC4612066          DOI: 10.3748/wjg.v9.i12.2839

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  41 in total

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Journal:  Lancet       Date:  2002-04-06       Impact factor: 79.321

2.  Abnormal endothelin B receptor vasomotor responses in patients with Hirschsprung's disease.

Authors:  D E Newby; F E Strachan; D J Webb
Journal:  QJM       Date:  2002-03

3.  A founding locus within the RET proto-oncogene may account for a large proportion of apparently sporadic Hirschsprung disease and a subset of cases of sporadic medullary thyroid carcinoma.

Authors:  Salud Borrego; Fred A Wright; Raquel M Fernández; Nita Williams; Manuel López-Alonso; Ramana Davuluri; Guillermo Antiñolo; Charis Eng
Journal:  Am J Hum Genet       Date:  2002-12-09       Impact factor: 11.025

4.  Novel mutations of the endothelin B receptor gene in patients with Hirschsprung's disease and their characterization.

Authors:  H Tanaka; K Moroi; J Iwai; H Takahashi; N Ohnuma; S Hori; M Takimoto; M Nishiyama; T Masaki; M Yanagisawa; S Sekiya; S Kimura
Journal:  J Biol Chem       Date:  1998-05-01       Impact factor: 5.157

5.  Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease.

Authors:  R Gath; A Goessling; K M Keller; S Koletzko; W Coerdt; H Müntefering; S Wirth; R M Hofstra; L Mulligan; C Eng; A von Deimling
Journal:  Gut       Date:  2001-05       Impact factor: 23.059

6.  A heterozygous endothelin 3 mutation in Waardenburg-Hirschsprung disease: is there a dosage effect of EDN3/EDNRB gene mutations on neurocristopathy phenotypes?

Authors:  V Pingault; N Bondurand; N Lemort; M Sancandi; I Ceccherini; J P Hugot; P S Jouk; M Goossens
Journal:  J Med Genet       Date:  2001-03       Impact factor: 6.318

7.  De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease.

Authors:  S M Ivanchuk; S M Myers; C Eng; L M Mulligan
Journal:  Hum Mol Genet       Date:  1996-12       Impact factor: 6.150

8.  Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.

Authors:  M Angrist; S Bolk; M Halushka; P A Lapchak; A Chakravarti
Journal:  Nat Genet       Date:  1996-11       Impact factor: 38.330

9.  Transgenic expression of the endothelin-B receptor prevents congenital intestinal aganglionosis in a rat model of Hirschsprung disease.

Authors:  C E Gariepy; S C Williams; J A Richardson; R E Hammer; M Yanagisawa
Journal:  J Clin Invest       Date:  1998-09-15       Impact factor: 14.808

10.  A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene.

Authors:  Yoshibumi Matsushima; Yusuke Shinkai; Yasuhito Kobayashi; Michihiro Sakamoto; Tetsuo Kunieda; Masayoshi Tachibana
Journal:  Mamm Genome       Date:  2002-01       Impact factor: 2.957

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  4 in total

1.  miR-618 rs2682818 C>A polymorphism decreases Hirschsprung disease risk in Chinese children.

Authors:  Yi Zheng; Tongyi Lu; Xiaoli Xie; Qiuming He; Lifeng Lu; Wei Zhong
Journal:  Biosci Rep       Date:  2020-05-29       Impact factor: 3.840

2.  Molecular cloning and characterization of the endothelin 3 gene in black bone sheep.

Authors:  Hesham Y A Darwish; Yuanyuan Zhang; Kai Cui; Zu Yang; Deping Han; Xianggui Dong; Huaming Mao; Weidong Deng; Xuemei Deng
Journal:  J Anim Sci Biotechnol       Date:  2018-06-25

3.  Waardenburg Syndrome Expression and Penetrance.

Authors:  Myeshia V Shelby
Journal:  J Rare Dis Res Treat       Date:  2017-12-10

4.  Identifying key genes associated with Hirschsprung's disease based on bioinformatics analysis of RNA-sequencing data.

Authors:  Wei-Kang Pan; Ya-Fei Zhang; Hui Yu; Ya Gao; Bai-Jun Zheng; Peng Li; Chong Xie; Xin Ge
Journal:  World J Pediatr       Date:  2017-01-25       Impact factor: 2.764

  4 in total

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