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Transfection of TRK-A into human neuroblastoma cells restores their ability to differentiate in response to nerve growth factor.
Uppsala universitet, Medicinska vetenskapsområdet, Medicinska fakulteten, Institutionen för genetik och patologi.
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1995 (English)In: Cell growth & differentiation, ISSN 1044-9523, Vol. 6, no 6, 727-736 p.Article in journal (Refereed) Published
Abstract [en]

Human neuroblastoma cell lines frequently express the TRK-A proto-oncogene and bind nerve growth factor (NGF) but do not differentiate when exposed to NGF. Transient transfection of an exogenous TRK-A gene into SH-SY5Y and LA-N-5 neuroblastoma cells restored the ability of these tumor cells to differentiate with NGF. Stable TRK-A-transfected SH-SY5Y cell clones were isolated, and they responded to NGF by autophosphorylation of p140trk-A, c-fos induction, morphological differentiation, and increased expression of two neuronal marker genes, neuropeptide tyrosine and GAP-43. In phorbol ester-induced differentiated wild-type cells, TRK-A expression was increased with no change in NGF responsiveness. Thus, the restoration of the NGF-induced differentiation pathway by exogenous TRK-A presents a system of NGF-responsive human cultured cells and focuses attention on the trk-A protein and its function or malfunction in neuroblastoma.

Place, publisher, year, edition, pages
1995. Vol. 6, no 6, 727-736 p.
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Medical and Health Sciences
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URN: urn:nbn:se:kau:diva-29806PubMedID: 7669728OAI: oai:DiVA.org:kau-29806DiVA: diva2:657584
Available from: 2013-10-20 Created: 2013-10-20 Last updated: 2013-11-07Bibliographically approved

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Nånberg, Eewa
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