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Human achaete-scute homologue 1 (HASH-1) is downregulated in differentiating neuroblastoma cells

Söderholm, Helena, 1969- (author)
Uppsala universitet,Institutionen för patologi,Sven Påhlman
Örtoft, Eva (author)
Department of Laboratory Medicine, Division of Molecular Medicine, Lund University, Malmö, Sweden
Johansson, Irja (author)
Department of Laboratory Medicine, Division of Molecular Medicine, Lund University, Malmö, Sweden
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Ljungberg, June (author)
Lund University,Lunds universitet,Genomik, diabetes och endokrinologi,Forskargrupper vid Lunds universitet,Genomics, Diabetes and Endocrinology,Lund University Research Groups,Department of Laboratory Medicine, Division of Molecular Medicine, Lund University, Malmö, Sweden
Larsson, Christer (author)
Lund University,Lunds universitet,Institutionen för translationell medicin,Medicinska fakulteten,Department of Translational Medicine,Faculty of Medicine,Department of Laboratory Medicine, Division of Molecular Medicine, Lund University, Malmö, Sweden
Axelson, Håkan (author)
Lund University,Lunds universitet,Institutionen för translationell medicin,Medicinska fakulteten,Department of Translational Medicine,Faculty of Medicine,Department of Laboratory Medicine, Division of Molecular Medicine, Lund University, Malmö, Sweden
Påhlman, Sven (author)
Lund University,Lunds universitet,Institutionen för translationell medicin,Medicinska fakulteten,Department of Translational Medicine,Faculty of Medicine,Department of Laboratory Medicine, Division of Molecular Medicine, Lund University, Malmö, Sweden
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 (creator_code:org_t)
Elsevier BV, 1999
1999
English.
In: Biochemical and Biophysical Research Communications. - : Elsevier BV. - 1090-2104 .- 0006-291X. ; 256:3, s. 557-563
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The mammalian achaete-scute homologue, MASH-1, is crucial for early development of the sympathetic nervous system and is transiently expressed in sympathetic neuroblasts during embryogenesis. Here we report that the human homologue (HASH-1) was expressed in all analyzed cell lines (6/6) derived from the sympathetic nervous system tumor neuroblastoma. The majority of small-cell lung carcinoma (4/5) cell lines tested expressed HASH-1, while other nonneuronal/non-neuroendocrine cell lines were negative. Induced differentiation of neuroblastoma cells resulted in HASH-1 downregulation. This occurred concomitant with induction of neurite outgrowth and expression of the neuronal marker genes GAP-43 and neuropeptide Y. Constitutive expression of exogenous HASH-1 did not alter the capacity of the neuroblastoma cells to differentiate in response to differentiation-inducing agents. It is concluded that moderate HASH-1 expression does not compromise the capacity of these cells to differentiate.

Subject headings

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

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