<?xml version="1.0" encoding="UTF-8"?>
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  <title>DSpace コレクション: 2019-9</title>
  <link rel="alternate" href="http://hdl.handle.net/11605/138" />
  <subtitle>2019-9</subtitle>
  <id>http://hdl.handle.net/11605/138</id>
  <updated>2026-04-01T11:40:22Z</updated>
  <dc:date>2026-04-01T11:40:22Z</dc:date>
  <entry>
    <title>膜型セリンプロテアーゼMT-SP1 によるCDCP1 切断を介した癌細胞の足場非依存性能の解析</title>
    <link rel="alternate" href="http://hdl.handle.net/11605/139" />
    <author>
      <name>澤山, 忠司</name>
    </author>
    <author>
      <name>上北, 尚正</name>
    </author>
    <id>http://hdl.handle.net/11605/139</id>
    <updated>2019-10-02T16:30:07Z</updated>
    <published>2019-08-31T15:00:00Z</published>
    <summary type="text">タイトル: 膜型セリンプロテアーゼMT-SP1 によるCDCP1 切断を介した癌細胞の足場非依存性能の解析
著者名: 澤山, 忠司; 上北, 尚正
抄録: CUB domain-containing protein 1 (CDCP1) is an important molecule for regulating　anchorage-independence involved in cancer metastasis. Recently, it was reported that the synthetic　substrate of CDCP1 is cleaved by Membrane-type serine protease 1(MT-SP1), however it is not clear that　this cleavage is involved in anchorage-independence. In this study, we investigated the effect of CDCP1　cleavage by MT-SP1 on anchorage-independence in cancer cells by soft agar assay using MT-SP1 siRNA　and uncleaved CDCP1 mutant (2RKAAres-F). As a result, cleavage of CDCP1 was inhibited in both　experiments, and then the anchorage independence was suppressed. Therefore, it is suggested that the　cleavage of CDCP1 by MT-SP1 is involved in the regulation of anchorage independence in cancer cells.</summary>
    <dc:date>2019-08-31T15:00:00Z</dc:date>
  </entry>
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