Literature DB >> 7795728

The analysis of p53 tumor suppressor gene in pineal parenchymal tumors.

I Tsumanuma1, M Sato, H Okazaki, R Tanaka, K Washiyama, T Kawasaki, T Kumanishi.   

Abstract

p53 gene mutation was examined in 9 pineal parenchymal tumors, 4 pineoblastomas and 5 pineocytomas, by the immunohistochemical and the polymerase chain reaction-mediated single strand conformation polymorphism (PCR-SSCP) analyses. In each case, immunohistochemical analysis revealed no positive staining for p53 protein with either PAb1801 or DO-1 antibody and PCR-SSCP analysis revealed no abnormal migration in exons 5 to 8 of the p53 gene. These findings suggested that p53 gene mutation is rarely related with the tumorigenesis of pineal parenchymal tumors.

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Year:  1995        PMID: 7795728

Source DB:  PubMed          Journal:  Noshuyo Byori        ISSN: 0914-8108


  4 in total

1.  Congenital pineoblastoma and parameningeal rhabdomyosarcoma: concurrent two embryonal tumors in a young infant.

Authors:  Funda Corapçíoğlu; M Memet Ozek; Aydin Sav; Deniz Uren
Journal:  Childs Nerv Syst       Date:  2005-11-09       Impact factor: 1.475

Review 2.  Molecular genetics of pineal region neoplasms.

Authors:  M D Taylor; T G Mainprize; J A Squire; J T Rutka
Journal:  J Neurooncol       Date:  2001-09       Impact factor: 4.130

3.  Histopathologic review of pineal parenchymal tumors identifies novel morphologic subtypes and prognostic factors for outcome.

Authors:  David R Raleigh; David A Solomon; Shane A Lloyd; Ann Lazar; Michael A Garcia; Penny K Sneed; Jennifer L Clarke; Michael W McDermott; Mitchel S Berger; Tarik Tihan; Daphne A Haas-Kogan
Journal:  Neuro Oncol       Date:  2016-06-09       Impact factor: 12.300

Review 4.  Molecular Classification and Management of Rare Pediatric Embryonal Brain Tumors.

Authors:  Patrick Sin-Chan; Bryan K Li; Ben Ho; Adriana Fonseca; Annie Huang
Journal:  Curr Oncol Rep       Date:  2018-07-11       Impact factor: 5.075

  4 in total

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