期刊
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES
卷 40, 期 3, 页码 202-208出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejps.2010.03.010
关键词
Peptide transporter; Dipeptides; Pancreatic cancer
资金
- Ishikawa Prefectural Government, Japan
- Ministry of Education, Science and Culture of Japan
- Sagawa Foundation for Promotion of Cancer Research
Oligopeptide transporters are abundantly expressed in various types of cancer cells. We here synthesized two novel dipeptides, L-phenylalanyl sarcosine (Phe-Sar) and 4-(4-methoxyphenyl)-L-phenylalanyl sarcosine (Bip(OMe)-Sar), and examined their effect on the growth of human pancreatic cancer AsPC-1 cells, which are known to highly express oligopeptide transporter PEPT1/SLC15A1. Growth of AsPC-1 cells was inhibited by these two peptides and a typical PEPT1/SLC15A1 substrate Gly-Sar. Growth inhibition by Gly-Sar, Phe-Sar and Bip(OMe)-Sar was concentration-dependent with half-maximal inhibitory concentration of 50, 0.91 and 0.55 mM, respectively. These peptides also inhibited PEPT1-mediated [(3)H]Gly-Sar uptake with half-maximal inhibitory concentration of 2.6, 0.81 and 0.27 mM, respectively. Thus, the rank order of the tumor cell growth inhibition by these three peptides was the same as that of PEPT1-inhibitory activity. Growth of AsPC-1 cells was also inhibited by 2-aminobicyclo(2,2,1)heptane-2-carboxylic acid (BCH), which is a typical inhibitor of amino acid transporter system L The growth inhibition by BCH and Gly-Sar was additive, suggesting that these compounds act at distinct loci. Oligopeptide transporters thus appear to be a promising target for inhibition of pancreatic cancer progression. These results also proposed the idea that oligopeptide transporter is required for growth of AsPC-1 cells. (C) 2010 Elsevier B.V. All rights reserved.
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