KLF10, transforming growth factor-β-inducible early gene 1, acts as a tumor suppressor

Ki Duk Song, Duk Jung Kim, Jong Eun Lee, Cheol Heui Yun, Woon Kyu Lee

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Krüppel-like factor 10 (KLF10) has been suggested to be a putative tumor suppressor. In the present study, we generated KLF10 deficient mice to explore this hypothesis in vivo. KLF10 deficient mice exhibited increased predisposition to skin tumorigenesis and markedly accelerated papilloma development after DMBA/TPA treatment. On the other hand, KLF10 deficient keratinocytes showed increased proliferation and apoptosis. In colony formation assays after oncogenic H-Ras transfection, KLF10 deficient mouse embryonic fibroblasts (MEFs) yielded more colonies than wild-type MEFs. Furthermore, KLF10 dose-dependently activated p21WAF1/CIP1 transcription, which was independent of p53 and Sp1 binding sites in p21WAF1/CIP1 promoter. This study demonstrates that KLF10 is a tumor suppressor and that it targets p21WAF1/CIP1 transcription.

Original languageEnglish
Pages (from-to)388-394
Number of pages7
JournalBiochemical and Biophysical Research Communications
Volume419
Issue number2
DOIs
Publication statusPublished - 2012 Mar 9

Fingerprint

Transforming Growth Factors
Transcription
Fibroblasts
Tumors
Genes
9,10-Dimethyl-1,2-benzanthracene
Assays
Neoplasms
Skin
Binding Sites
Apoptosis
Papilloma
Keratinocytes
Transfection
Carcinogenesis

All Science Journal Classification (ASJC) codes

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

Song, Ki Duk ; Kim, Duk Jung ; Lee, Jong Eun ; Yun, Cheol Heui ; Lee, Woon Kyu. / KLF10, transforming growth factor-β-inducible early gene 1, acts as a tumor suppressor. In: Biochemical and Biophysical Research Communications. 2012 ; Vol. 419, No. 2. pp. 388-394.
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KLF10, transforming growth factor-β-inducible early gene 1, acts as a tumor suppressor. / Song, Ki Duk; Kim, Duk Jung; Lee, Jong Eun; Yun, Cheol Heui; Lee, Woon Kyu.

In: Biochemical and Biophysical Research Communications, Vol. 419, No. 2, 09.03.2012, p. 388-394.

Research output: Contribution to journalArticle

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