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        <datestamp>2024-10-31T08:00:10Z</datestamp>
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          <dc:title xml:lang="en">Galectin-9 suppresses the proliferation of gastric cancer cells in vitro</dc:title>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">Takano, Jitsuko</jpcoar:creatorName>
            <jpcoar:creatorName xml:lang="ja">髙野, 実子</jpcoar:creatorName>
            <jpcoar:creatorName xml:lang="ja-Kana">タカノ, ジツコ</jpcoar:creatorName>
          </jpcoar:creator>
          <dcterms:accessRights rdf:resource="http://purl.org/coar/access_right/c_abf2">open access</dcterms:accessRights>
          <dc:rights xml:lang="en">Copyright © Spandidos Publications 2015.</dc:rights>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">caspase-cleaved keratin 18</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">gastric cancer</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">galectin-9</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">apoptosis</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">microRNAs</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">insulin-like growth factor 1 receptor</jpcoar:subject>
          <jpcoar:subject xml:lang="en" subjectScheme="Other">angiogenesis</jpcoar:subject>
          <datacite:description xml:lang="en" descriptionType="Abstract">Abstract
Gastric cancer is the second-leading cause of cancer-related mortality worldwide, and the prognosis of advanced gastric cancer remains poor. Galectin-9 (Gal-9) is a tandem-repeat-type galectin that has recently been demonstrated to exert anti-proliferative effects on various types of cancer cells. The aim of our present study was to evaluate the effects of Gal-9 on human gastric cancer cells and the expression levels of microRNAs (miRNAs) associated with the antitumor effects of Gal-9 in vitro. In our initial experiments, Gal-9 suppressed the proliferation of gastric cancer cell lines in vitro. Our data further revealed that Gal-9 increased caspase-cleaved keratin 18 (CCK18) levels in gastric cancer cells. Additionally, Gal-9 reduced the phosphorylation of vascular endothelial growth factor receptor-3 (VEGFR-3) and insulin-like growth factor-1 receptor (IGF-1R). Furthermore, miRNA expression levels were markedly altered with Gal-9 treatment in vitro. In conclusion, Gal-9 suppressed the proliferation of human gastric cancer cells by inducing apoptosis. These findings suggest that Gal-9 could be a potential therapeutic target in the treatment of gastric cancer.</datacite:description>
          <dc:language>eng</dc:language>
          <dc:type rdf:resource="http://purl.org/coar/resource_type/c_db06">doctoral thesis</dc:type>
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            <jpcoar:relatedIdentifier identifierType="DOI">https://doi.org/10.3892/or.2015.4452</jpcoar:relatedIdentifier>
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            <jpcoar:relatedIdentifier identifierType="NAID">500001356634</jpcoar:relatedIdentifier>
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          <dcndl:dissertationNumber>甲第637号</dcndl:dissertationNumber>
          <dcndl:degreeName xml:lang="ja">博士（医学）</dcndl:degreeName>
          <dcndl:dateGranted>2016-03-24</dcndl:dateGranted>
          <jpcoar:degreeGrantor>
            <jpcoar:nameIdentifier nameIdentifierScheme="kakenhi">16201</jpcoar:nameIdentifier>
            <jpcoar:degreeGrantorName xml:lang="ja">香川大学</jpcoar:degreeGrantorName>
            <jpcoar:degreeGrantorName xml:lang="en">Kagawa University</jpcoar:degreeGrantorName>
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            <datacite:date dateType="Available">2020-11-09</datacite:date>
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