Literature DB >> 11748642

Gene expression patterns in melanocytic cells: candidate markers for early stage and malignant transformation.

Clifton B Meije1, Theodorus B M Hakvoort, Guido W M Swart, Wiete Westerhof, Wouter H Lamers, Pranab K Das.   

Abstract

Different stages of differentiation of human melanocytic cells, such as normal melanocytes, naevus and melanoma cells, reflect distinct gene expression patterns. A PCR-based subtractive hybridization and display method was applied to identify genes that are differentially expressed in melanocytic cells in relation to early stage and malignant transformation. This resulted in the identification of a number of candidate cDNAs differentially expressed among melanocytes, naevus cells, and (non)-metastatic melanoma cells. Out of this collection of cDNAs, 16 clones were screened that comprised 12 novel genes, one previously identified expressed sequence tag related to vesicular trafficking (Ras-related protein Rab5b). The other three were also known genes that were either related to cell motility (beta-tubulin), pre-mRNA splicing (small nuclear protein U1A), or of unknown function (the human TI227-H gene). The differential expression patterns of Rab5b and two novel gene fragments (pCMa1, pCMn2) were further assessed in melanocytic cells. pCMa1 was expressed more in metastatic melanoma than in primary melanoma cells. In contrast, pCMn2 was expressed in both non-metastatic and metastatic melanoma cells, but was not detectable in either normal melanocytes or naevus cells. The Ras-related protein Rab5b showed lower levels of expression in highly metastatic than in other melanoma cells. These three cDNAs may therefore be involved in the early stage and malignant transformation of melanocytes. Copyright 2001 John Wiley & Sons, Ltd.

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Year:  2002        PMID: 11748642     DOI: 10.1002/path.1017

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  2 in total

1.  Rab5 is required in metastatic cancer cells for Caveolin-1-enhanced Rac1 activation, migration and invasion.

Authors:  Jorge Díaz; Pablo Mendoza; Rina Ortiz; Natalia Díaz; Lisette Leyton; Dwayne Stupack; Andrew F G Quest; Vicente A Torres
Journal:  J Cell Sci       Date:  2014-03-21       Impact factor: 5.285

2.  Response projected clustering for direct association with physiological and clinical response data.

Authors:  Sung-Gon Yi; Taesung Park; Jae K Lee
Journal:  BMC Bioinformatics       Date:  2008-01-31       Impact factor: 3.169

  2 in total

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