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    <subfield code="a">10.1016/j.ctarc.2021.100355</subfield>
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    <subfield code="a">eng</subfield>
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    <subfield code="a">Al-Wasaby, S.</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">In vivo potential of recombinant granulysin against human melanoma</subfield>
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  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2021</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
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    <subfield code="a">9-kDa granulysin is a protein expressed into the granules of human cytotoxic T lymphocytes (CTL) and natural killer (NK) cells. It has been shown to exert cytolysis on microbes and tumors. We showed previously that 9-kDa granulysin exerted cell death by apoptosis in vitro on hematological tumor cell lines and also on cells from B-cell chronic lymphocytic leukemia (B-CLL) patients. In addition, we have shown the anti-tumor efficiency of granulysin as a single agent in two in vivo models of human tumor development in athymic mice, the MDA-MB-231 mammary adenocarcinoma and the NCI-H929 multiple myeloma, without signs of overt secondary effects by itself. In this work, we have tested recombinant 9-kDa granulysin in an in vivo and especially aggressive model of melanoma development, xenografted UACC62 cells in athymic mice. Recombinant granulysin was administered once UACC62-derived tumors were detectable and it substantially retarded the in vivo development of this aggressive tumor. We could also detect apoptosis induction and increased NK cell infiltration inside granulysin-treated tumor tissues. These observations are especially interesting given the possibility of treating melanoma by intra-tumor injection.</subfield>
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    <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/SAF2016-76338-R</subfield>
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    <subfield code="a">Oncology</subfield>
    <subfield code="c">2021</subfield>
    <subfield code="d">Q3</subfield>
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    <subfield code="a">Cancer Research</subfield>
    <subfield code="c">2021</subfield>
    <subfield code="d">Q3</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Guerrero-Ochoa, P.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-1657-4792</subfield>
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  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Ibáñez-Pérez, R.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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    <subfield code="a">Soler, R.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
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    <subfield code="a">Conde, B.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-4115-9766</subfield>
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    <subfield code="a">Martínez-Lostao, L.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0003-3043-147X</subfield>
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    <subfield code="a">Anel, A.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0002-5175-8394</subfield>
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    <subfield code="1">1003</subfield>
    <subfield code="2">443</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Anatom.Histolog.Humanas</subfield>
    <subfield code="c">Area Histología</subfield>
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    <subfield code="1">1011</subfield>
    <subfield code="2">566</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Microb.Ped.Radio.Sal.Pú.</subfield>
    <subfield code="c">Área Inmunología</subfield>
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    <subfield code="1">1002</subfield>
    <subfield code="2">060</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Bioq.Biolog.Mol. Celular</subfield>
    <subfield code="c">Área Bioquímica y Biolog.Mole.</subfield>
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    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Bioq.Biolog.Mol. Celular</subfield>
    <subfield code="c">Área Biología Celular</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">27 (2021), 100355 [7 pp.]</subfield>
    <subfield code="t">Cancer Treatment and Research Communications</subfield>
    <subfield code="x">2468-2942</subfield>
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