Skip to main content
Cytotechnology logoLink to Cytotechnology
. 1997 Nov;25(1-3):221–225. doi: 10.1023/A:1007915917201

Inhibitory effect of serum from rats administered with coffee on the proliferation and invasion of rat ascites hepatoma cells

Yutaka Miura, Tamio Furuse, Kazumi Yagasaki
PMCID: PMC3466754  PMID: 22358895

Abstract

The action of coffee on the proliferation and invasion of a rat ascites hepatoma cell line of AH109A was investigated using in vitro and ex vivo assay systems. When rats were given oral intubation of instant coffee powder solution, the sera of those rats had the potent inhibitory activity on both the proliferation and invasion of AH109A. The activity of rat serum was both time- and dose-dependent. The instant coffee powder also inhibited the proliferation and invasion of AH109A in vitro. These results indicate that coffee has anti-proliferative and anti-invasive activity both in vitro and ex vivo. They also suggest that some anti-proliferative and anti-invasive material(s), which may be the ingredient(s) of coffee or their metabolites, appear in rat serum when rats are given oral intubation of coffee, although a possibility that host defense systems may be activated by the oral intubation of coffee cannot be ruled out.

Keywords: coffee, hepatoma, invasion, oral intubation, proliferation

Full Text

The Full Text of this article is available as a PDF (54.1 KB).

References

  1. Akedo H, Shinkai K, Mukai M, Mori Y, Tateishi R, Tanaka K, Yamamoto R, Morishita T. Interaction of rat ascites hepatoma cells with cultured mesothelial cell layers: A model for tumor invasion. Cancer Res. 1986;46:2416–2422. [PubMed] [Google Scholar]
  2. Albini A, Iwamoto Y, Kleinman HK, Matrin G, Aaronson SA, Kozlowski JM, McEwan RN. A rapid in vitro assay for quantitating the invasive potential of tumor cells. Cancer Res. 1987;47:3239–3245. [PubMed] [Google Scholar]
  3. Armstrong PB, Quigley JP, Sidebottom E. Transepithelial invasion and intramesenchymal infiltration of chick embryo chorioallantois by tumor cell lines. Cancer Res. 1982;42:1826–1837. [PubMed] [Google Scholar]
  4. Fidler IJ, Gersten DM, Hart IR. The biology of cancer invasion and metastasis. Adv. Cancer Res. 1978;28:149–250. doi: 10.1016/S0065-230X(08)60648-X. [DOI] [PubMed] [Google Scholar]
  5. Koshihara Y, Neichi T, Murota S, Lao A, Fujimoto Y, Tatsuno T. Selective inhibition of 5-lipoxygenase by natural compounds isolated from chinese plants, Artemisia rubripes Nakai. FEBS Lett. 1983;158:41–44. doi: 10.1016/0014-5793(83)80672-3. [DOI] [PubMed] [Google Scholar]
  6. Liotta L, Rao CN, Barsky SH. Tumor invasion and the extracellular matrix. Lab Invest. 1983;49:636–649. [PubMed] [Google Scholar]
  7. Liu X-H, Connolly JM, Rose DP. Eicosanoids as mediators of linoleic acid-stimulated invasion and type IV collagenase production by a metastatic human breast cancer cell line. Clin Exp Metastasis. 1996;14:145–152. doi: 10.1007/BF00121211. [DOI] [PubMed] [Google Scholar]
  8. Mareel MM. Recent aspects of tumor invasiveness. Int Rev Exp Pathol. 1980;22:65–129. [PubMed] [Google Scholar]
  9. Miura Y, Shiomi H, Sakai F, Yagasaki K. Assay systems for screening food components that have anti-proliferative and anti-invasive activity to rat ascites hepatoma cells: In vitro and ex vivo effects of green tea extract. Cytotechnology. 1997;23:127–132. doi: 10.1023/A:1007951231617. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Mosmann T. Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J Immuno Methods. 1983;65:55–63. doi: 10.1016/0022-1759(83)90303-4. [DOI] [PubMed] [Google Scholar]
  11. Mukai M, Shinkai K, Tateishi R, Mori Y, Akedo H. Macrophage potentiation of invasive capacity of rat ascites hepatoma cells. Cancer Res. 1987;47:2167–2171. [PubMed] [Google Scholar]
  12. Noel A, Calle A, Emonard HP, Nusgens BV, Simar L, Foidart J, Lapiereb CM, Foidart J-M. Invasion of reconstituted basement membrane matrix is not correlated with the malignant metastatic cell phenotype. Cancer Res. 1991;51:405–414. [PubMed] [Google Scholar]
  13. Poste G, Doll J, Hart IR, Fidler IJ. In vitro selection of murine B16 melanoma variants with enhanced tissue-invasive properties. Cancer Res. 1980;40:1636–1644. [PubMed] [Google Scholar]
  14. Reich R, Martin GR. Identification of arachidonic acid pathways required for the invasive and metastatic activity of malignant tumor cells. Prostaglandins. 1996;51:1–17. doi: 10.1016/0090-6980(95)00154-9. [DOI] [PubMed] [Google Scholar]
  15. Shinkai K, Mukai M, Akedo H. Superoxide radical potentiates invasive capacity of rat ascites hepatoma cells in vitro. Cancer Lett. 1986;32:7–13. doi: 10.1016/0304-3835(86)90033-9. [DOI] [PubMed] [Google Scholar]
  16. Welch DR, Lobl TJ, Seftor EA, Wack PJ, Aeed PA, Yohem KH, Seftor REB, Hendrix MJC. Use of the membrane invasion culture system (MICS) as a screen for anti-invasive agents. Int J Cancer. 1989;43:449–457. doi: 10.1002/ijc.2910430318. [DOI] [PubMed] [Google Scholar]
  17. Yagasaki K, Tanabe T, Ishihara K, Funabiki R, et al. Modulation of the proliferation of cultured hepatoma cells by urea cycle-related amino acids. In: Murakami H, et al., editors. Animal Cell Technology: Basic and Applied Aspects. The Netherlands: Kluwer Academic Publishers; 1992. pp. 257–263. [Google Scholar]

Articles from Cytotechnology are provided here courtesy of Springer Science+Business Media B.V.

RESOURCES