Mechanism Underlying NaF-induced Apoptosis and Cell Cycle Arrest on G361 Human Melanoma Cell Line.
10.11637/kjpa.2011.24.4.203
- Author:
Do Kyun KIM
1
;
Hyeon Jin SOHN
;
In Ryoung KIM
;
Gyoo Cheon KIM
;
Bong Soo PARK
;
Hyun Ho KWAK
Author Information
1. Department of Oral Anatomy, School of Dentistry, Pusan National University, Busan, Korea. kwakhh@pusan.ac.kr
- Publication Type:Original Article
- Keywords:
NaF;
Apoptosis;
Cell cycle arrest;
Human melanoma cells
- MeSH:
Apoptosis;
Blotting, Western;
Caspase 3;
Caspase 6;
Caspase 7;
Caspase 9;
Cell Cycle;
Cell Cycle Checkpoints;
Cell Death;
Cell Line;
Cell Proliferation;
Cell Survival;
Cytochromes c;
Cytosol;
Dental Caries;
Dentistry;
DNA;
DNA Fragmentation;
Down-Regulation;
Eating;
Electrophoresis;
Flow Cytometry;
Fluorides;
Humans;
Immunohistochemistry;
In Situ Nick-End Labeling;
Melanoma;
Microscopy, Confocal;
Mitochondria;
Oral Health;
Proteasome Endopeptidase Complex;
Proteins;
Up-Regulation
- From:Korean Journal of Physical Anthropology
2011;24(4):203-216
- CountryRepublic of Korea
- Language:English
-
Abstract:
Fluoride is widely used in dentistry to prevent dental caries, even though the safety of fluoride is a controversial issue. There are no known adverse effects of long-term fluoride ingestion for caries prevention, but an overdose can cause serious acute toxicity. Nevertheless it is accepted that fluoride is an important material for oral health. This study was undertaken to investigate the modulation of cell cycle-related proteins and apoptosis induction underlying mechanism by NaF treatment on G361 human melanoma cell line. The viability of G361 cells and the growth inhibition of G361 cells were assessed by MTT assay and clonogenic assay respectively. Hoechst staining, DNA electrophoresis and TUNEL staining were conducted to observe G361 cells undergoing apoptosis. G361 cells were treated with NaF, and Western blotting, immunocytochemistry, confocal microscopy, FACScan flow cytometry, MMP activity and proteasome activity were performed. NaF treatment in G361 cells resulted in a time- and does-dependent decrease of cell viability and a does-dependent inhibition of cell growth, and induced apoptotic cell death. And tested G361 cells showed several lines of apoptotic manifestation such as nuclear condensation, DNA fragmentation, the reduction of MMP and proteasome activity, the decrease of DNA contents, the release of cytochrome c into cytosol, the translocation of AIF and DFF40 (CAD) onto nuclei, a significant shift of Bax/Bcl-2 ratio, and the activation of caspase-9, caspase-7, caspase-6, caspase-3, PARP, Lamin A/C and DFF45 (ICAD). Furthermore, NaF resulted in down-regulation of the G1 cell cycle-related proteins, and up-regulation of p53. Taken collectively, our present findings demonstrate that NaF strongly inhibits cell proliferation by modulating the expression of the G1 cell cycle-related proteins and induces apoptosis via proteasome, mitochondria and caspase cascades in G361 cells.
