Inhibition of in vitro tumor cell invasion by transmethylation inhibitors
- PMID: 2555319
- PMCID: PMC5917839
- DOI: 10.1111/j.1349-7006.1989.tb01703.x
Inhibition of in vitro tumor cell invasion by transmethylation inhibitors
Abstract
Three inhibitors of S-adenosylmethionine-mediated transmethylation, 5'-methylthioadenosine (MTA), 2'-deoxyadenosine and sinefungin, inhibited in vitro invasion by a highly invasive clone (Cl-30) of rat ascites hepatoma cells, AH 130 (AH cells). Difluoromethylthioadenosine (DFMTA), a non-metabolizable derivative of MTA, also caused strong inhibition of invasion at concentrations that did not suppress the growth of the tumor cells. Cl-30 cells precultured in methionine-depleted medium showed decreased invasiveness. DFMTA was also effective on the invasion by fibrosarcoma, B16 melanoma and human lung carcinoma cell lines.
Similar articles
-
Effects of methylthiodeoxyadenosine and its analogs on in vitro invasion of rat ascites hepatoma cells and methylation of their phospholipids.Jpn J Cancer Res. 1991 Oct;82(10):1104-11. doi: 10.1111/j.1349-7006.1991.tb01764.x. Jpn J Cancer Res. 1991. PMID: 1955377 Free PMC article.
-
Comparative effects of L-methionine, S-adenosyl-L-methionine and 5'-methylthioadenosine on the growth of preneoplastic lesions and DNA methylation in rat liver during the early stages of hepatocarcinogenesis.Anticancer Res. 1991 Jul-Aug;11(4):1617-24. Anticancer Res. 1991. PMID: 1684097
-
Effect of 5'-difluoromethylthioadenosine, an inhibitor of methylthioadenosine phosphorylase, on proliferation of cultured cells.J Cell Physiol. 1987 Nov;133(2):372-6. doi: 10.1002/jcp.1041330223. J Cell Physiol. 1987. PMID: 3119605
-
The role of 5'-methylthioadenosine on rat calvaria cell differentiation.Biochem Biophys Res Commun. 1992 Jan 31;182(2):817-23. doi: 10.1016/0006-291x(92)91805-z. Biochem Biophys Res Commun. 1992. PMID: 1734884
-
Methylthioadenosine.Int J Biochem Cell Biol. 2004 Nov;36(11):2125-30. doi: 10.1016/j.biocel.2003.11.016. Int J Biochem Cell Biol. 2004. PMID: 15313459 Review.
Cited by
-
Methylation inhibitors can increase the rate of cytosine deamination by (cytosine-5)-DNA methyltransferase.Nucleic Acids Res. 1996 Aug 15;24(16):3267-75. doi: 10.1093/nar/24.16.3267. Nucleic Acids Res. 1996. PMID: 8774911 Free PMC article.
-
DNA methylation as a target for drug design.Pharm Res. 1998 Feb;15(2):175-87. doi: 10.1023/a:1011946030404. Pharm Res. 1998. PMID: 9523301 Review.
-
Enhanced paracellular barrier function of rat mesothelial cells partially protects against cancer cell penetration.Br J Cancer. 1996 Aug;74(3):439-45. doi: 10.1038/bjc.1996.378. Br J Cancer. 1996. PMID: 8695361 Free PMC article.
-
Effects of methylthiodeoxyadenosine and its analogs on in vitro invasion of rat ascites hepatoma cells and methylation of their phospholipids.Jpn J Cancer Res. 1991 Oct;82(10):1104-11. doi: 10.1111/j.1349-7006.1991.tb01764.x. Jpn J Cancer Res. 1991. PMID: 1955377 Free PMC article.
-
Serum requirement for in vitro invasion by tumor cells.Jpn J Cancer Res. 1991 May;82(5):493-6. doi: 10.1111/j.1349-7006.1991.tb01877.x. Jpn J Cancer Res. 1991. PMID: 1905695 Free PMC article.
References
-
- ) Akedo , H. , Shinkai , K. , Mukai , M. , Mori , Y. , Tateishi , R. , Tanaka , K. , Yamamoto , R. and Morishita , T.Interaction of rat ascites hepatoma cells with cultured mesothelial cell layers: a model for tumor invasion . Cancer Res. , 46 , 2416 – 2422 ( 1986. ). - PubMed
-
- ) Shinkai , K. , Mukai , M. and Akedo , H.Superoxide radical potentiates invasive capacity of rat ascites hepatoma cells in vitro . Cancer Lett. , 32 , 7 – 13 ( 1986. ). - PubMed
-
- ) Mukai , M. , Shinkai , K. , Tateishi , R. , Mori , Y. and Akedo , H.Macrophage potentiation of invasive capacity of rat ascites hepatoma cells . Cancer Res. , 47 , 2167 – 2171 ( 1987. ). - PubMed
-
- ) Shinkai , K. , Mukai , M. and Akedo , H.Induction of invasive capacity of tumor cells by oxygen radicals . In “ Free Radicals in Clinical Medicine ,” ed. Kondo M. , Oyanagi Y. and Yoshikawa T. , pp. 63 – 71 ( 1987. ). Nihon‐Igakukan; , Tokyo ( in Japanese ).
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical