Subcellular localization of apurinic endonuclease 1 promotes lung tumor aggressiveness via NF-κB activation

H. H. Wu, Y. W. Cheng, J. T. Chang, T. C. Wu, W. S. Liu, C. Y. Chen, H. Lee

Research output: Contribution to journalArticle

34 Citations (Scopus)

Abstract

Apurinic endonuclease 1 (Ape1) is not only involved in base excision repair, but also activates some transcriptional factors through its redox activity. However, which subcellular localization of Ape1 is involved in the activation of transcriptional factor remains unclear. We first observed that Cox-2 expression was associated with cytoplasmic Ape1 expression in lung tumors and cancer cell lines. We thus hypothesize that nuclear factor (NF)-B is activated by cytoplasmic Ape1 to cause Cox-2 expression. Herein, we generated cytoplasmic and nuclear Ape1 in Ape1-knockdown lung cancer cells by exogenous expression of Ape1 containing various deletions and/or mutations of the nuclear localization sequence. It was observed that cytoplasmic Ape1, but not nuclear Ape1, induced Cox-2 expression through NF-B activation. NF-B activation by cytoplasmic Ape1 was diminished by the Ape1 redox activity inhibitor resveratrol. Cells expressing cytoplasmic Ape1 exhibited tumor progression and metastasis in vitro and in vivo as xenografts, but cells expressing nuclear Ape1 did not. Patients with tumors containing elevated cytoplasmic Ape1 had a poor prognosis and a 3.722-fold risk of tumor recurrence and/or metastasis. Cytoplasmic Ape1 could therefore enhance lung tumor malignancy through NF-B activation, suggesting that combination of cisplatin and specific redox inhibitor could improve chemotherapeutic response in patients with tumors containing elevated cytoplasmic Ape1.

Original languageEnglish
Pages (from-to)4330-4340
Number of pages11
JournalOncogene
Volume29
Issue number30
DOIs
Publication statusPublished - Jul 29 2010
Externally publishedYes

Fingerprint

DNA-(Apurinic or Apyrimidinic Site) Lyase
Lung
Neoplasms
Oxidation-Reduction
Lung Neoplasms
Neoplasm Metastasis

Keywords

  • Cox-2
  • cytoplasmic Ape1
  • lung tumor metastasis
  • NF-κB

ASJC Scopus subject areas

  • Molecular Biology
  • Cancer Research
  • Genetics

Cite this

Wu, H. H., Cheng, Y. W., Chang, J. T., Wu, T. C., Liu, W. S., Chen, C. Y., & Lee, H. (2010). Subcellular localization of apurinic endonuclease 1 promotes lung tumor aggressiveness via NF-κB activation. Oncogene, 29(30), 4330-4340. https://doi.org/10.1038/onc.2010.178

Subcellular localization of apurinic endonuclease 1 promotes lung tumor aggressiveness via NF-κB activation. / Wu, H. H.; Cheng, Y. W.; Chang, J. T.; Wu, T. C.; Liu, W. S.; Chen, C. Y.; Lee, H.

In: Oncogene, Vol. 29, No. 30, 29.07.2010, p. 4330-4340.

Research output: Contribution to journalArticle

Wu, HH, Cheng, YW, Chang, JT, Wu, TC, Liu, WS, Chen, CY & Lee, H 2010, 'Subcellular localization of apurinic endonuclease 1 promotes lung tumor aggressiveness via NF-κB activation', Oncogene, vol. 29, no. 30, pp. 4330-4340. https://doi.org/10.1038/onc.2010.178
Wu, H. H. ; Cheng, Y. W. ; Chang, J. T. ; Wu, T. C. ; Liu, W. S. ; Chen, C. Y. ; Lee, H. / Subcellular localization of apurinic endonuclease 1 promotes lung tumor aggressiveness via NF-κB activation. In: Oncogene. 2010 ; Vol. 29, No. 30. pp. 4330-4340.
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