Literature DB >> 2158936

Protein gene product (PGP) 9.5 as a reliable marker in primitive neuroectodermal tumours--an immunohistochemical study of 21 childhood cases.

M D Harris1, I E Moore, P V Steart, R O Weller.   

Abstract

A number of antibodies to neural proteins have been used to demonstrate neuronal differentiation in primitive neuroectodermal tumours. One of them is protein gene product (PGP) 9.5, a neuronal protein isolated from brain, whose function is unknown at present. We have studied differentiation in 21 cases of primitive neuroectodermal tumours of the CNS in children. Immunocytochemical staining was performed for such neuronal markers as: PGP 9.5, neuron specific enolase and synaptophysin, a glycosylated protein associated with synaptic vesicles. Positive staining for PGP 9.5 was present in 16 cases (strong staining in 12), for neuron-specific enolase in 16 cases (strong staining in 10) and for synaptophysin in 10 cases (strong staining in six). Both PGP 9.5 and synaptophysin showed a clear staining pattern with less non-specific background than with neuron-specific enolase. Our findings demonstrate the value of using more than one antibody marker in assessing neuronal differentiation in tumours. The high incidence of positive staining with antibody to PGP 9.5 suggests that this is an essential marker in the panel of antibodies used for the identification of primitive neuroectodermal tumours.

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Year:  1990        PMID: 2158936     DOI: 10.1111/j.1365-2559.1990.tb01114.x

Source DB:  PubMed          Journal:  Histopathology        ISSN: 0309-0167            Impact factor:   5.087


  2 in total

1.  Pleomorphic primitive neuroectodermal tumor with glial and neuronal differentiation: clinical, pathological, cultural, and chromosomal analysis of a case.

Authors:  Yuji Uematsu; Rie Takehara; Mina Shimizu; Yoshiyuki Tanaka; Toru Itakura; Norihiko Komai
Journal:  J Neurooncol       Date:  2002-08       Impact factor: 4.130

2.  A continuous cell line (KK-2) from a supratentorial primitive neuroectodermal tumor.

Authors:  H Ito; T Kameya; T Suwa; C Wada; N Kawano
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

  2 in total

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