Literature DB >> 7621416

Absence of mutation at the GAP-related domain of the neurofibromatosis type 1 gene in sporadic neurofibrosarcomas and other bone and soft tissue sarcomas.

L Gómez1, C Barrios, A Kreicbergs, A Zetterberg, A Pestaña, J S Castresana.   

Abstract

The NF1 gene encodes neurofibromin, a GTPase-activating protein containing a GAP-related domain (NF1-GRD) that is capable of downregulating ras by stimulating ras intrinsic GTPase activity. We tested 44 sarcomas, nine of which corresponded to sporadic neurofibrosarcomas, for mutations at the NF1-GRD by the polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique, finding no mutation in every sample tested. We suggest that inactivation of the NF1-GRD by gene mutation seems not to be an important event in the tumorigenesis of sarcomas.

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Year:  1995        PMID: 7621416     DOI: 10.1016/0165-4608(94)00267-f

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  3 in total

1.  NF1 deletions in S-100 protein-positive and negative cells of sporadic and neurofibromatosis 1 (NF1)-associated plexiform neurofibromas and malignant peripheral nerve sheath tumors.

Authors:  A Perry; K A Roth; R Banerjee; C E Fuller; D H Gutmann
Journal:  Am J Pathol       Date:  2001-07       Impact factor: 4.307

2.  Epithelioid hemangioendothelioma and multiple thoraco-lumbar lateral meningoceles: two rare pathological entities in a patient with NF-1.

Authors:  C Reis; E Carneiro; J Fonseca; P Pereira; R Vaz; R Pinto; A F Capelinha; J M Lopes; A Salgado
Journal:  Neuroradiology       Date:  2005-02-02       Impact factor: 2.804

Review 3.  A Review of the Molecular Pathways Involved in Resistance to BRAF Inhibitors in Patients with Advanced-Stage Melanoma.

Authors:  Yangzi Tian; Weinan Guo
Journal:  Med Sci Monit       Date:  2020-04-10
  3 in total

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