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Expression of Fanconi anemia D2 gene and its function in Hela and MCF10A cells

  • Hyun Park Woo*
  • *Corresponding author for this work
  • Brigham and Women’s Hospital

Research output: Contribution to journalJournal articlepeer-review

Abstract

Fanconi Anemia (FA) is a disease with autosomal recessive inheritance and characterized by developmental abnormalities, progressive bone marrow failure and cancer predisposition. Especially, the phenotypes of FA cells show the extreme sensitivity towards oxygen and DNA crosslinking agents such as diepoxybutane and mitomycin C (MMC). In the current study, I made the retroviruses which expressed FANCD2 gene for making the stable cell lines, Hela (cervical carcinoma) and MCF10A (breast). I could detect the expression of FANCD2 protein in the Hela and MCF10A stable cells after the puromycin selection. When I incubated the cells lines with crosslinking agents, MMC, the MCF10A cells which expressed the exogenous FANCD2 was resistant to the MMC, compared with the MCF10 parent cells. But the Hela cells which expressed the FANCD2 did not show the resistance to the MMC. Together, I conclude that FANCD2 protein is an important factor for resistance to the crosslinking agent, MMC in the MCF10A breast cell, but not the Hela cervical carcinoma cells.

Original languageEnglish
Pages (from-to)339-344
Number of pages6
JournalKorean Journal of Genetics
Volume26
Issue number4
StatePublished - 2004.12

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • FANCD2
  • Fanconi anemia
  • Hela cell
  • MCF10A cell

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