Literature DB >> 28101359

Effect of combined treatment with micelle-incorporated cisplatin (NC-6004) and S-1 on human gastric cancer xenografts.

Masahisa Kudo1, Yoshiyuki Yamamoto2, Yoshikatsu Koga2, Tetsuya Hamaguchi3, Tetsuo Akimoto4, Masahiro Yasunaga2, Yasuhiro Matsumura2.   

Abstract

Combination therapy with S-1 and cisplatin (CDDP) is the standard chemotherapy for advanced gastric cancer in Japan; however, its administration requires hospitalization for hydration to prevent nephrotoxicity from CDDP. By contrast, NC-6004 appears to reduce the renal toxicity of CDDP and may be used on an outpatient basis. Thus, the effects of combined treatment with S-1 and NC-6004 were compared with those of S-1 and CDDP in a human gastric cancer model. In vitro cytotoxic effects were investigated in 44As3Luc, MKN45 and MKN74 human gastric cancer cell lines. The effects of NC-6004 and 5-fluorouracil (5-FU) were compared with the effects of CDDP and 5-FU using the combination index method. The in vivo antitumor effects of S-1/NC-6004 and S-1/CDDP were evaluated in mice bearing 44As3Luc xenografts. Both combinations exhibited synergistic activity in MKN45 and MKN74 cells and additive effects in 44As3Luc cells. Moreover, the in vivo antitumor effects did not differ between the S-1/NC-6004 and S-1/CDDP treatment groups. However, a significantly lower body weight loss was observed in S-1/NC-6004-treated mice compared with the S-1/CDDP-treated mice. Our data warrant a clinical evaluation of S-1/NC-6004 combination therapy.

Entities:  

Keywords:  NC-6004; S-1; drug delivery system; enhanced permeability and retention effect; gastric cancer

Year:  2016        PMID: 28101359      PMCID: PMC5228101          DOI: 10.3892/mco.2016.1070

Source DB:  PubMed          Journal:  Mol Clin Oncol        ISSN: 2049-9450


  14 in total

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Journal:  Adv Drug Deliv Rev       Date:  2010-05-10       Impact factor: 15.470

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3.  A photon counting technique for quantitatively evaluating progression of peritoneal tumor dissemination.

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Journal:  Cancer Res       Date:  2006-08-01       Impact factor: 12.701

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Journal:  Lancet Oncol       Date:  2008-02-20       Impact factor: 41.316

7.  A new concept for macromolecular therapeutics in cancer chemotherapy: mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs.

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Journal:  Cancer Res       Date:  1986-12       Impact factor: 12.701

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Journal:  Br J Cancer       Date:  2011-02-01       Impact factor: 7.640

9.  Cisplatin-incorporated polymeric micelles eliminate nephrotoxicity, while maintaining antitumor activity.

Authors:  Y Mizumura; Y Matsumura; T Hamaguchi; N Nishiyama; K Kataoka; T Kawaguchi; W J Hrushesky; F Moriyasu; T Kakizoe
Journal:  Jpn J Cancer Res       Date:  2001-03

10.  Cisplatin-incorporating polymeric micelles (NC-6004) can reduce nephrotoxicity and neurotoxicity of cisplatin in rats.

Authors:  H Uchino; Y Matsumura; T Negishi; F Koizumi; T Hayashi; T Honda; N Nishiyama; K Kataoka; S Naito; T Kakizoe
Journal:  Br J Cancer       Date:  2005-09-19       Impact factor: 7.640

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