Chronic cigarette smoke extract treatment selects for apoptotic dysfunction and mitochondrial mutations in minimally transformed oral keratinocytes

Steven S. Chang, Wei Wen Jiang, Ian Smith, Chad Glazer, Wen Yue Sun, Suhail Mithani, Joseph A. Califano

Research output: Contribution to journalArticle

Abstract

Cigarette smoke demonstrates a carcinogenic effect through chronic exposure, not acute exposures. However, current cell line models study only the acute effects of cigarette smoke. Using a cell line model, we compared the effects of acute versus chronic cigarette smoke extract (CSE) on mitochondria in minimally transformed oral keratinocytes (OKF6). OKF6 cells were treated with varying concentrations of CSE for 6 months. Cells were analyzed monthly by flow cytometry for mitochondrial membrane potential (MMP), cytochrome c release, caspase 3 activation and viability after CSE exposure. At each time point, the same assays were performed after 24 hr of valinomycin (MMP-depolarizing agent) treatment. The mitochondrial DNA of chronically CSE-treated cells was sequenced. After 6 months of CSE treatment, the cells were increasingly resistant to CSE-mediated and valinomycin-induced cell death. In addition, chronic CSE treatment caused chronic depolarization of MMP, cytochrome c release and caspase activation. Cells grown in the presence of only CSE vapor also exhibited the same resistance and chronic baseline apoptotic activation. Mitochondrial DNA sequencing found that chronic CSE-treated cells had more amino acid-changing mitochondrial mutations than acutely treated cells. CSE treatment of normal cells select for apoptotic dysfunction as well as mitochondrial mutations. These findings suggest that chronic tobacco exposure induces carcinogenesis via selection of apoptosis resistance and mitochondrial mutation in addition to previously known genotoxic effects that were found by acute treatments. Chronic models of tobacco exposure on upper aerodigestive epithelia may be more insightful than models of acute exposure in studying head and neck carcinogenesis.

Original languageEnglish (US)
Pages (from-to)19-27
Number of pages9
JournalInternational Journal of Cancer
Volume126
Issue number1
DOIs
StatePublished - Jan 1 2010

Fingerprint

Keratinocytes
Smoke
Tobacco Products
Mutation
Mitochondrial Membrane Potential
Cell Extracts
Valinomycin
Cytochromes c
Mitochondrial DNA
Tobacco
Carcinogenesis
Cell Line
Caspases
DNA Sequence Analysis
Caspase 3
Flow Cytometry
Mitochondria
Cell Death
Neck
Epithelium

Keywords

  • Apoptosis
  • Cigarette smoke extract
  • CSE
  • Keratinocytes
  • Mitochondria

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Chronic cigarette smoke extract treatment selects for apoptotic dysfunction and mitochondrial mutations in minimally transformed oral keratinocytes. / Chang, Steven S.; Jiang, Wei Wen; Smith, Ian; Glazer, Chad; Sun, Wen Yue; Mithani, Suhail; Califano, Joseph A.

In: International Journal of Cancer, Vol. 126, No. 1, 01.01.2010, p. 19-27.

Research output: Contribution to journalArticle

Chang, Steven S. ; Jiang, Wei Wen ; Smith, Ian ; Glazer, Chad ; Sun, Wen Yue ; Mithani, Suhail ; Califano, Joseph A. / Chronic cigarette smoke extract treatment selects for apoptotic dysfunction and mitochondrial mutations in minimally transformed oral keratinocytes. In: International Journal of Cancer. 2010 ; Vol. 126, No. 1. pp. 19-27.
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