Abstract |
Adenosine triphosphate ( ATP) has been shown to be an inhibitory or a stimulatory agent for cell growth in various types of cells. Here, we studied the effects of extracellular ATP on two pancreatic cancer cell lines, PK-1 and YAPC established by us. In both cell lines, ATP inhibited cell growth in a time- and dose-dependent manner, whereas the same doses of ATP stimulated DNA synthesis. Flow cytometric analysis of the cells incubated with or without ATP demonstrated the ATP-induced striking increase in cells at S-phase. The same analysis showed also the increase in sub-G0/G1 population in the same analysis and the electrophoretic pattern of DNA showed the occurrence of ATP-induced cell disintegration likely to be apoptosis. We suggest that extracellular ATP is cytotoxic for pancreatic cancer cells because of its induction of cell cycle arrest at S-phase and cell death, possibly apoptosis, overcoming the promotion of the entry into S-phase.
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Authors | Takayuki Yamada, Fumikazu Okajima, Mohammed Akbar, Hideaki Tomura, Torao Narita, Tatsuya Yamada, Susumu Ohwada, Yasuo Morishita, Yoichi Kondo |
Journal | Oncology reports
(Oncol Rep)
2002 Jan-Feb
Vol. 9
Issue 1
Pg. 113-7
ISSN: 1021-335X [Print] Greece |
PMID | 11748467
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- DNA, Neoplasm
- Formazans
- Tetrazolium Salts
- MTT formazan
- Adenosine Triphosphate
- Thymidine
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Topics |
- Adenosine Triphosphate
(pharmacology)
- Apoptosis
(drug effects)
- Cell Cycle
(drug effects)
- Cell Division
(drug effects)
- DNA, Neoplasm
(drug effects)
- Flow Cytometry
- Formazans
- Humans
- Pancreatic Neoplasms
(drug therapy, pathology)
- Tetrazolium Salts
- Thymidine
(metabolism)
- Tumor Cells, Cultured
(drug effects)
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