Literature DB >> 10768863

Brachyury is expressed by human teratocarcinoma cells in the absence of mesodermal differentiation.

P J Gokhale1, A M Giesberts, P W Andrews.   

Abstract

Reverse transcription-PCR and Northern and Western blot analyses indicate that mRNA and protein encoded by the Brachyury gene are expressed by the pluripotent human embryonal carcinoma cell line NTERA2 and are only modestly down-regulated during retinoic acid-induced differentiation. This differentiation occurs along a neural lineage, with no obvious evidence of the formation of mesodermal derivatives. Several other human embryonal carcinoma cell lines that do not differentiate, a yolk sac carcinoma cell line and two choriocarcinoma cell lines, also express readily detectable levels of Brachyury mRNA and protein. Thus, in human teratocarcinomas, Brachyury expression is not necessarily an indicator of commitment to mesodermal differentiation.

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Year:  2000        PMID: 10768863

Source DB:  PubMed          Journal:  Cell Growth Differ        ISSN: 1044-9523


  8 in total

1.  Surface antigens of human embryonic stem cells: changes upon differentiation in culture.

Authors:  Jonathan S Draper; Christine Pigott; James A Thomson; Peter W Andrews
Journal:  J Anat       Date:  2002-03       Impact factor: 2.610

Review 2.  Embryonic stem cell-derived trophoblast differentiation: a comparative review of the biology, function, and signaling mechanisms.

Authors:  M Giakoumopoulos; T G Golos
Journal:  J Endocrinol       Date:  2013-02-25       Impact factor: 4.286

3.  Nuclear Brachyury Expression Is Consistent in Chordoma, Common in Germ Cell Tumors and Small Cell Carcinomas, and Rare in Other Carcinomas and Sarcomas: An Immunohistochemical Study of 5229 Cases.

Authors:  Markku Miettinen; Zengfeng Wang; Jerzy Lasota; Christopher Heery; Jeffrey Schlom; Claudia Palena
Journal:  Am J Surg Pathol       Date:  2015-10       Impact factor: 6.394

4.  Assessment of pluripotency and multilineage differentiation potential of NTERA-2 cells as a model for studying human embryonic stem cells.

Authors:  Rajarshi Pal; Geeta Ravindran
Journal:  Cell Prolif       Date:  2006-12       Impact factor: 6.831

5.  Transcriptional program of bone morphogenetic protein-2-induced epithelial and smooth muscle differentiation of pluripotent human embryonal carcinoma cells.

Authors:  Rajendrakumar S V Chadalavada; Jane Houldsworth; Adam B Olshen; George J Bosl; Lorenz Studer; R S K Chaganti
Journal:  Funct Integr Genomics       Date:  2005-02-03       Impact factor: 3.410

Review 6.  Model systems for studying trophoblast differentiation from human pluripotent stem cells.

Authors:  Toshihiko Ezashi; Bhanu Prakash V L Telugu; R Michael Roberts
Journal:  Cell Tissue Res       Date:  2012-03-17       Impact factor: 5.249

Review 7.  TGFβ Family Signaling Pathways in Pluripotent and Teratocarcinoma Stem Cells' Fate Decisions: Balancing Between Self-Renewal, Differentiation, and Cancer.

Authors:  Olga Gordeeva
Journal:  Cells       Date:  2019-11-23       Impact factor: 6.600

8.  Human pluripotent embryonal carcinoma NTERA2 cl.D1 cells maintain their typical morphology in an angiomyogenic medium.

Authors:  Pedro D Simões; Teresa Ramos
Journal:  J Negat Results Biomed       Date:  2007-04-18
  8 in total

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