Chios Gum Mastic Induces Cell Cycle Arrest and Apoptosis in YD9 Human Oral Squamous Carcinoma Cells.
10.11637/kjpa.2008.21.1.55
- Author:
Jae Hyoun PARK
1
;
Gyoo Cheon KIM
;
Hyun Ho KWAK
;
In Ryoung KIM
;
Seung Eun LEE
;
Jin CHUNG
;
Hae Ryoun PARK
;
Sang Hun SHIN
;
Soo Hyun CHOI
;
Chul Hoon KIM
;
Chang Ok NAM
;
Bong Soo PARK
Author Information
1. Department of Oral Anatomy, School of Dentistry, Pusan National University, Korea. parkbs@pusan.ac.kr
- Publication Type:In Vitro ; Original Article
- Keywords:
Chios gum mastic (CGM);
Apoptosis;
Human oral squamous carcinoma cell line;
Cell cycle arrest
- MeSH:
Apoptosis;
Blotting, Western;
Carcinoma, Squamous Cell;
Cell Cycle;
Cell Cycle Checkpoints;
Cell Death;
Cell Line;
Cyclin D1;
Cyclin D3;
Dietary Supplements;
DNA;
Electrophoresis;
Flow Cytometry;
Gingiva;
Humans;
Immunohistochemistry;
Membrane Potential, Mitochondrial;
Microscopy, Confocal;
Mitochondria;
Pistacia;
Proteasome Endopeptidase Complex;
Proteins;
Resins, Plant;
Trees
- From:Korean Journal of Physical Anthropology
2008;21(1):55-68
- CountryRepublic of Korea
- Language:English
-
Abstract:
Chios gum mastic (CGM) is obtained from the stem and leaves of Pistacia lentiscus trees and has been extensively used for centuries in Mediterranean and Middle Eastern countries, both as a dietary supplement and herbal remedy. This study was undertaken to examine in vitro effects of cytotoxicity and growth inhibition, and the molecular mechanism underlying modulation of cell cycle and induction of apoptosis in YD9 human oral squamous carcinoma cell line treated with CGM. The viability of YD9 cells and human normal keratinocyes (HaCaT cells), and the growth inhibition of YD9 cells were assessed by the MTT assay and clonogenic assay respectively. The hoechst staining and DNA electrophoresis were conducted to observe the YD9 cells undergoing apoptosis. YD9 cells were treated with CGM, and Western blotting, immunocytochemistry, confocal microscopy and FACScan flow cytometry were conducted. Mitochondrial membrane potential change and proteasome activity were measured. CGM treatment on YD9 cells resulted in a does-dependent inhibition of cell growth and induced apoptotic cell death. And tested YD9 cells showed several lines of apoptotic manifestation. Flow cytometric analysis revealed that CGM resulted in G1 arrest in cell cycle progression which was associated with decrease in the protein expression of cyclin D1, cyclin D3, Cdk2 and Cdk4, and increase in the protein expression of p21(WAF1/CIP1) and p53. These results demonstrate that CGM induces G1 the cell cycle arrest via the modulation of cell cycle-related proteins, and apoptosis via mitochondria and caspase pathway in YD9 cells, suggesting that CGM can be considered as a novel therapeutic strategy for human oral squamous cell carcinoma from its strong cell cycle arrest and apoptosis-inducing activity.
