Defined genetic events associated with the spontaneous in vitro transformation of E1A/Ras-expressing human IMR90 fibroblasts

Douglas X. Mason, Daniel Keppler, Jun Zhang, Tonya J. Jackson, Yvette R. Seger, Seiichi Matsui, Fleurette Abreo, John Kenneth Cowell, Gregory J. Hannon, S. W.Scott W. Lowe, Athena W. Lin

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

In contrast to rodent cells, normal human fibroblasts are generally resistant to neoplastic transformation in vitro. Here, we report the derivation and characterization of a spontaneously transformed cell line from normal human IMR90 fibroblasts transduced with E1A and Ras oncogenes. Unlike the parental, non-tumorigenic E1A/Ras-expressing IMR90 cells, these spontaneously transformed cells displayed aberrant growth potential in vitro and were capable of tumorigenesis in vivo. In contrast to the parental E1A/Ras-expressing cells, both the spontaneously transformed cells and cells derived from resultant tumors displayed specific t(7q;8q) and t(5q;17) structural chromosomal changes. Chromosome 8q contains c-Myc, which is capable of activating the telomerase catalytic subunit hTERT. Notably, upregulation of c-Myc, hTERT and telomerase activity were detected only in the tumorigenic cells. Transduction of Myc siRNA into the tumorigenic cells led to a concomitant downregulation of hTERT. Furthermore, transduction of Myc or hTERT into the non-tumorigenic E1A/Ras-expressing IMR90 cells was able to confer tumorigenesis on these cells. These studies suggest that the t(7;8) translocation may result in Myc overexpression and its subsequent activation of hTERT, which may contribute to the tumorigenicity of the IMR90 cells. Furthermore, this report describes additional successful neoplastic transformation of human IMR90 fibroblasts by defined genetic elements. The spontaneously transformed cells we have derived provide a valuable model system for the study of neoplastic transformation.

Original languageEnglish (US)
Pages (from-to)350-359
Number of pages10
JournalCarcinogenesis
Volume27
Issue number2
DOIs
StatePublished - Feb 1 2006
Externally publishedYes

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Fibroblasts
Telomerase
In Vitro Techniques
Carcinogenesis
Transformed Cell Line
ras Genes
Small Interfering RNA
Rodentia
Up-Regulation
Down-Regulation
Chromosomes
Growth

ASJC Scopus subject areas

  • Cancer Research

Cite this

Mason, D. X., Keppler, D., Zhang, J., Jackson, T. J., Seger, Y. R., Matsui, S., ... Lin, A. W. (2006). Defined genetic events associated with the spontaneous in vitro transformation of E1A/Ras-expressing human IMR90 fibroblasts. Carcinogenesis, 27(2), 350-359. https://doi.org/10.1093/carcin/bgi264

Defined genetic events associated with the spontaneous in vitro transformation of E1A/Ras-expressing human IMR90 fibroblasts. / Mason, Douglas X.; Keppler, Daniel; Zhang, Jun; Jackson, Tonya J.; Seger, Yvette R.; Matsui, Seiichi; Abreo, Fleurette; Cowell, John Kenneth; Hannon, Gregory J.; Lowe, S. W.Scott W.; Lin, Athena W.

In: Carcinogenesis, Vol. 27, No. 2, 01.02.2006, p. 350-359.

Research output: Contribution to journalArticle

Mason, DX, Keppler, D, Zhang, J, Jackson, TJ, Seger, YR, Matsui, S, Abreo, F, Cowell, JK, Hannon, GJ, Lowe, SWSW & Lin, AW 2006, 'Defined genetic events associated with the spontaneous in vitro transformation of E1A/Ras-expressing human IMR90 fibroblasts', Carcinogenesis, vol. 27, no. 2, pp. 350-359. https://doi.org/10.1093/carcin/bgi264
Mason, Douglas X. ; Keppler, Daniel ; Zhang, Jun ; Jackson, Tonya J. ; Seger, Yvette R. ; Matsui, Seiichi ; Abreo, Fleurette ; Cowell, John Kenneth ; Hannon, Gregory J. ; Lowe, S. W.Scott W. ; Lin, Athena W. / Defined genetic events associated with the spontaneous in vitro transformation of E1A/Ras-expressing human IMR90 fibroblasts. In: Carcinogenesis. 2006 ; Vol. 27, No. 2. pp. 350-359.
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