Areca nut extract and arecoline induced the cell cycle arrest but not apoptosis of cultured oral KB epithelial cells

Association of glutathione, reactive oxygen species and mitochondrial membrane potential

M. C. Chang, Y. S. Ho, P. H. Lee, C. P. Chan, J. J. Lee, L. J. Hahn, Y. J. Wang, J. H. Jeng

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Abstract

There are 600 million betel quid (BQ) chewers in the world. BQ chewing is a major etiologic factor of oral cancer. Areca nut (AN) and arecoline may inhibit the growth of oral mucosal fibroblasts (OMF) and keratinocytes. In this study, AN extract (100-800 μg/ml) and arecoline (20-120 μM) inhibited the growth of oral KB cells by 36-90 and 15-75%, respectively. Exposure to arecoline (>0.2 mM) for 24 h induced G 2/M cell cycle arrest of OMF and KB cells. Areca nut extract (>400 μg/ml) also induced G 2/M arrest of KB cells, being preceded by S-phase arrest at 7-h of exposure. No evident sub-G 0/G 1 peak was noted. Marked retraction and intracellular vacuoles formation of OMF and KB cells were observed. Glutathione (GSH) level, mitochondrial membrane potential (Δβm) and H 2O 2 production of KB cells were measured by flow cytometry. GSH level [indicated by 5-chloromethyl-fluorescein (CMF) fluorescence] was depleted by 24-h exposure of KB cells to arecoline (0.4-1.2 mM) and AN extract (800-1200 μg/ml), with increasing the percentage of cells in low CMF fluorescence. By contrast, arecoline (0.1-1.2 mM) and AN extract (800-1200 μg/ml) induced decreasing and increasing H 2O 2 production (by 2′,7′-dichloro-fluorescein fluorescence), respectively. Hyperpolarization of Δβm (increasing of rhodamine uptake) was noted by 24-h exposure of KB cells to arecoline (0.4-1.2 mM) and AN extract (800-1200 μg/ml). AN extract (100-1200 μg/ml) and arecoline (0.1-1.2 mM) induced little DNA fragmentation on KB cells within 24 h. These results indicate that AN ingredients are crucial in the pathogenesis of oral submucous fibrosis (OSF) and oral cancer by differentially inducing the dysregulation of cell cycle control, Δβm, GSH level and intracellular H 2O 2 production, these events being not coupled with cellular apoptosis.

Original languageEnglish
Pages (from-to)1527-1535
Number of pages9
JournalCarcinogenesis
Volume22
Issue number9
Publication statusPublished - 2001

Fingerprint

Arecoline
Areca
KB Cells
Nuts
Mitochondrial Membrane Potential
Cell Cycle Checkpoints
Glutathione
Reactive Oxygen Species
Epithelial Cells
Apoptosis
Fluorescein
Fibroblasts
Fluorescence
Mouth Neoplasms
Oral Submucous Fibrosis
Rhodamines
Mastication
DNA Fragmentation
Growth
Vacuoles

ASJC Scopus subject areas

  • Cancer Research

Cite this

Areca nut extract and arecoline induced the cell cycle arrest but not apoptosis of cultured oral KB epithelial cells : Association of glutathione, reactive oxygen species and mitochondrial membrane potential. / Chang, M. C.; Ho, Y. S.; Lee, P. H.; Chan, C. P.; Lee, J. J.; Hahn, L. J.; Wang, Y. J.; Jeng, J. H.

In: Carcinogenesis, Vol. 22, No. 9, 2001, p. 1527-1535.

Research output: Contribution to journalArticle

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abstract = "There are 600 million betel quid (BQ) chewers in the world. BQ chewing is a major etiologic factor of oral cancer. Areca nut (AN) and arecoline may inhibit the growth of oral mucosal fibroblasts (OMF) and keratinocytes. In this study, AN extract (100-800 μg/ml) and arecoline (20-120 μM) inhibited the growth of oral KB cells by 36-90 and 15-75{\%}, respectively. Exposure to arecoline (>0.2 mM) for 24 h induced G 2/M cell cycle arrest of OMF and KB cells. Areca nut extract (>400 μg/ml) also induced G 2/M arrest of KB cells, being preceded by S-phase arrest at 7-h of exposure. No evident sub-G 0/G 1 peak was noted. Marked retraction and intracellular vacuoles formation of OMF and KB cells were observed. Glutathione (GSH) level, mitochondrial membrane potential (Δβm) and H 2O 2 production of KB cells were measured by flow cytometry. GSH level [indicated by 5-chloromethyl-fluorescein (CMF) fluorescence] was depleted by 24-h exposure of KB cells to arecoline (0.4-1.2 mM) and AN extract (800-1200 μg/ml), with increasing the percentage of cells in low CMF fluorescence. By contrast, arecoline (0.1-1.2 mM) and AN extract (800-1200 μg/ml) induced decreasing and increasing H 2O 2 production (by 2′,7′-dichloro-fluorescein fluorescence), respectively. Hyperpolarization of Δβm (increasing of rhodamine uptake) was noted by 24-h exposure of KB cells to arecoline (0.4-1.2 mM) and AN extract (800-1200 μg/ml). AN extract (100-1200 μg/ml) and arecoline (0.1-1.2 mM) induced little DNA fragmentation on KB cells within 24 h. These results indicate that AN ingredients are crucial in the pathogenesis of oral submucous fibrosis (OSF) and oral cancer by differentially inducing the dysregulation of cell cycle control, Δβm, GSH level and intracellular H 2O 2 production, these events being not coupled with cellular apoptosis.",
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T2 - Association of glutathione, reactive oxygen species and mitochondrial membrane potential

AU - Chang, M. C.

AU - Ho, Y. S.

AU - Lee, P. H.

AU - Chan, C. P.

AU - Lee, J. J.

AU - Hahn, L. J.

AU - Wang, Y. J.

AU - Jeng, J. H.

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N2 - There are 600 million betel quid (BQ) chewers in the world. BQ chewing is a major etiologic factor of oral cancer. Areca nut (AN) and arecoline may inhibit the growth of oral mucosal fibroblasts (OMF) and keratinocytes. In this study, AN extract (100-800 μg/ml) and arecoline (20-120 μM) inhibited the growth of oral KB cells by 36-90 and 15-75%, respectively. Exposure to arecoline (>0.2 mM) for 24 h induced G 2/M cell cycle arrest of OMF and KB cells. Areca nut extract (>400 μg/ml) also induced G 2/M arrest of KB cells, being preceded by S-phase arrest at 7-h of exposure. No evident sub-G 0/G 1 peak was noted. Marked retraction and intracellular vacuoles formation of OMF and KB cells were observed. Glutathione (GSH) level, mitochondrial membrane potential (Δβm) and H 2O 2 production of KB cells were measured by flow cytometry. GSH level [indicated by 5-chloromethyl-fluorescein (CMF) fluorescence] was depleted by 24-h exposure of KB cells to arecoline (0.4-1.2 mM) and AN extract (800-1200 μg/ml), with increasing the percentage of cells in low CMF fluorescence. By contrast, arecoline (0.1-1.2 mM) and AN extract (800-1200 μg/ml) induced decreasing and increasing H 2O 2 production (by 2′,7′-dichloro-fluorescein fluorescence), respectively. Hyperpolarization of Δβm (increasing of rhodamine uptake) was noted by 24-h exposure of KB cells to arecoline (0.4-1.2 mM) and AN extract (800-1200 μg/ml). AN extract (100-1200 μg/ml) and arecoline (0.1-1.2 mM) induced little DNA fragmentation on KB cells within 24 h. These results indicate that AN ingredients are crucial in the pathogenesis of oral submucous fibrosis (OSF) and oral cancer by differentially inducing the dysregulation of cell cycle control, Δβm, GSH level and intracellular H 2O 2 production, these events being not coupled with cellular apoptosis.

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