Literature DB >> 27795433

Efficient Transformation of Primary Human Mesenchymal Stromal Cells by Adenovirus Early Region 1 Oncogenes.

Thomas Speiseder1, Helga Hofmann-Sieber1, Estefanía Rodríguez1, Anna Schellenberg2, Nuray Akyüz2, Judith Dierlamm2, Thilo Spruss3, Claudia Lange4, Thomas Dobner5.   

Abstract

Previous observations that human amniotic fluid cells (AFC) can be transformed by human adenovirus type 5 (HAdV-5) E1A/E1B oncogenes prompted us to identify the target cells in the AFC population that are susceptible to transformation. Our results demonstrate that one cell type corresponding to mesenchymal stem/stroma cells (hMSCs) can be reproducibly transformed by HAdV-5 E1A/E1B oncogenes as efficiently as primary rodent cultures. HAdV-5 E1-transformed hMSCs exhibit all properties commonly associated with a high grade of oncogenic transformation, including enhanced cell proliferation, anchorage-independent growth, increased growth rate, and high telomerase activity as well as numerical and structural chromosomal aberrations. These data confirm previous work showing that HAdV preferentially transforms cells of mesenchymal origin in rodents. More importantly, they demonstrate for the first time that human cells with stem cell characteristics can be completely transformed by HAdV oncogenes in tissue culture with high efficiency. Our findings strongly support the hypothesis that undifferentiated progenitor cells or cells with stem cell-like properties are highly susceptible targets for HAdV-mediated cell transformation and suggest that virus-associated tumors in humans may originate, at least in part, from infections of these cell types. We expect that primary hMSCs will replace the primary rodent cultures in HAdV viral transformation studies and are confident that these investigations will continue to uncover general principles of viral oncogenesis that can be extended to human DNA tumor viruses as well. IMPORTANCE: It is generally believed that transformation of primary human cells with HAdV-5 E1 oncogenes is very inefficient. However, a few cell lines have been successfully transformed with HAdV-5 E1A and E1B, indicating that there is a certain cell type which is susceptible to HAdV-mediated transformation. Interestingly, all those cell lines have been derived from human embryonic tissue, albeit the exact cell type is not known yet. We show for the first time the successful transformation of primary human mesenchymal stromal cells (hMSCs) by HAdV-5 E1A and E1B. Further, we show upon HAdV-5 E1A and E1B expression that these primary progenitor cells exhibit features of tumor cells and can no longer be differentiated into the adipogenic, chondrogenic, or osteogenic lineage. Hence, primary hMSCs represent a robust and novel model system to elucidate the underlying molecular mechanisms of adenovirus-mediated transformation of multipotent human progenitor cells.
Copyright © 2016 American Society for Microbiology.

Entities:  

Keywords:  DNA tumor viruses; E1A; E1B; hMSCs; host-virus interactions; human tumor viruses; viral transformation and carcinogenesis

Mesh:

Substances:

Year:  2016        PMID: 27795433      PMCID: PMC5165183          DOI: 10.1128/JVI.01782-16

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  53 in total

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Authors:  K Weber; U Mock; B Petrowitz; U Bartsch; B Fehse
Journal:  Gene Ther       Date:  2009-12-17       Impact factor: 5.250

2.  A multicolor panel of novel lentiviral "gene ontology" (LeGO) vectors for functional gene analysis.

Authors:  Kristoffer Weber; Udo Bartsch; Carol Stocking; Boris Fehse
Journal:  Mol Ther       Date:  2008-02-12       Impact factor: 11.454

3.  The adenovirus E4orf6 protein can promote E1A/E1B-induced focus formation by interfering with p53 tumor suppressor function.

Authors:  M Nevels; S Rubenwolf; T Spruss; H Wolf; T Dobner
Journal:  Proc Natl Acad Sci U S A       Date:  1997-02-18       Impact factor: 11.205

4.  Maintenance of differentiation potential of human bone marrow mesenchymal stem cells immortalized by human telomerase reverse transcriptase gene despite [corrected] extensive proliferation.

Authors:  Basem M Abdallah; Mandana Haack-Sørensen; Jorge S Burns; Birgitte Elsnab; Franz Jakob; Peter Hokland; Moustapha Kassem
Journal:  Biochem Biophys Res Commun       Date:  2005-01-21       Impact factor: 3.575

5.  Hemangioendothelioma of bone in a patient with a constitutional supernumerary marker.

Authors:  S R Rogatto; C A Rainho; Z M Zhang; F Figueiredo; J Barbieri-Neto; S M Georgetto; J A Squire
Journal:  Cancer Genet Cytogenet       Date:  1999-04

6.  Acute nonlymphocytic leukemia following lung cancer in a patient with a constitutional supernumerary chromosome.

Authors:  M Minamihisamatsu; J S Gregorio; Y Onozawa; T Ishihara
Journal:  Cancer Genet Cytogenet       Date:  1988-10-15

Review 7.  Modelling the molecular circuitry of cancer.

Authors:  William C Hahn; Robert A Weinberg
Journal:  Nat Rev Cancer       Date:  2002-05       Impact factor: 60.716

8.  Downregulation of telomerase reverse transcriptase mRNA expression by wild type p53 in human tumor cells.

Authors:  D Xu; Q Wang; A Gruber; M Björkholm; Z Chen; A Zaid; G Selivanova; C Peterson; K G Wiman; P Pisa
Journal:  Oncogene       Date:  2000-10-26       Impact factor: 9.867

9.  Comparison of gene-transfer efficiency in human embryonic stem cells.

Authors:  Feng Cao; Xiaoyan Xie; Timothy Gollan; Li Zhao; Kazim Narsinh; Randall J Lee; Joseph C Wu
Journal:  Mol Imaging Biol       Date:  2009-06-24       Impact factor: 3.488

10.  Expression of E1A in terminally differentiated muscle cells reactivates the cell cycle and suppresses tissue-specific genes by separable mechanisms.

Authors:  M Tiainen; D Spitkovsky; P Jansen-Dürr; A Sacchi; M Crescenzi
Journal:  Mol Cell Biol       Date:  1996-10       Impact factor: 4.272

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  3 in total

Review 1.  Updated summary of genome editing technology in human cultured cells linked to human genetics studies.

Authors:  Tatsuo Miyamoto; Silvia Natsuko Akutsu; Shinya Matsuura
Journal:  J Hum Genet       Date:  2017-10-11       Impact factor: 3.172

2.  Engineered Sleeping Beauty Transposon as Efficient System to Optimize Chimp Adenoviral Production.

Authors:  Samantha Baldassarri; Daniela Benati; Federica D'Alessio; Clarissa Patrizi; Eleonora Cattin; Michela Gentile; Angelo Raggioli; Alessandra Recchia
Journal:  Int J Mol Sci       Date:  2022-07-07       Impact factor: 6.208

3.  Differential Regulation of Cellular FAM111B by Human Adenovirus C Type 5 E1 Oncogenes.

Authors:  Wing-Hang Ip; Britta Wilkens; Anastasia Solomatina; Judith Martin; Michael Melling; Paloma Hidalgo; Luca D Bertzbach; Thomas Speiseder; Thomas Dobner
Journal:  Viruses       Date:  2021-05-28       Impact factor: 5.048

  3 in total

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