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Roles of JNK/NRF2 pathway on hemin-induced heme oxygenase-1 activation in MCF-7 human breast cancer cells

  • Hye Yeon Jang
  • , On Yu Hong
  • , Eun Yong Chung
  • , Kwang Hyun Park*
  • , Jong Suk Kim
  • *Corresponding author for this work
  • Jeonbuk National University
  • The Catholic University of Korea
  • Nambu University
  • Chonnam National University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Heme oxygenase-1 (HO-1) is highly induced in various human disease states, including cancer, indicating that HO-1 is an emerging target of cancer therapy. In this study, we investigated that the mechanisms of hemin-induced HO-1 expression and its signaling pathways in human breast cancer cell. We used MCF-7 cells, a human breast cancer cell line. Hemin increased HO-1 expression in MCF-7 cells in a dose-and time-dependent manner. Hemin enhanced HO-1 expression through the activation of c-Jun N-terminal kinases (JNK) signaling pathway. Hemin also induced activation of Nrf2, a major transcription factor of HO-1 expression. These responses in MCF-7 cells were completely blocked by pretreatment with brazilin, a HO-1 regulator. These results indicated that brazilin inhibits hemin-induced HO-1 expressions through inactivation of JNK/Nrf2 in MCF-7 cells. Thus, our findings suggest that HO-1 is an important anticancer-target of brazilin in human breast cancer.

Original languageEnglish
Article number268
JournalMedicina (Lithuania)
Volume56
Issue number6
DOIs
StatePublished - 2020.06

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

  • Brazilin
  • Breast cancer
  • Heme oxygenase-1
  • Hemin
  • JNK
  • MCF-7
  • Nrf2

Quacquarelli Symonds(QS) Subject Topics

  • Medicine

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