Bcl-XL prevents serum deprivation-induced oxidative stress mediated by Romo1

Seung Baek Lee, Hyung Jung Kim, Jungar Shin, Sung Tae Kang, Seong Man Kang, Young Do Yoo

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

B-cell lymphoma-extra large (Bcl-XL) has been known to suppress serum deprivation-induced cell death, while reactive oxygen species modulator 1 (Romol) is responsible for a serum deprivation-induced increase in reactive oxygen species (ROS). Therefore, we investigated whether Bcl-XL expression could inhibit the serum deprivation-induced increase in ROS and cell death, which are mediated by Romol. We found that Bcl-XL expression effectively blocked serum deprivation- and Romol-triggered ROS generation. Bcl-XL also inhibited apoptotic cell death induced by both serum deprivation and oxidative stress. From these results, we suggest that increased Bcl-XL expression, which is observed in many cancer cells, confers resistance to oxidative stress in the cancer cells by suppressing Romol-mediated oxidative stress.

Original languageEnglish
Pages (from-to)1337-1342
Number of pages6
JournalOncology Reports
Volume25
Issue number5
DOIs
Publication statusPublished - 2011 May 1

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B-Cell Lymphoma
Reactive Oxygen Species
Oxidative Stress
Serum
Cell Death
Neoplasms

Keywords

  • B-cell lymphoma-extra large
  • Reactive oxygen species
  • Reactive oxygen species modulator 1
  • Serum deprivation

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Bcl-XL prevents serum deprivation-induced oxidative stress mediated by Romo1. / Lee, Seung Baek; Kim, Hyung Jung; Shin, Jungar; Kang, Sung Tae; Kang, Seong Man; Yoo, Young Do.

In: Oncology Reports, Vol. 25, No. 5, 01.05.2011, p. 1337-1342.

Research output: Contribution to journalArticle

Lee, Seung Baek ; Kim, Hyung Jung ; Shin, Jungar ; Kang, Sung Tae ; Kang, Seong Man ; Yoo, Young Do. / Bcl-XL prevents serum deprivation-induced oxidative stress mediated by Romo1. In: Oncology Reports. 2011 ; Vol. 25, No. 5. pp. 1337-1342.
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