Cargando…
An obstructive role of NK cells on metastatic growth of clear-cell sarcoma cells in a xenoplant murine model
Clear cell sarcoma (CCS) affects the deep soft tissues in young adults and is known to have high rates of metastasis, including lymphatic metastasis. In our previous study an xenoplant model of CCS was established, which exhibited local tumor growth, lymphatic metastasis, and distant metastasis in S...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690248/ https://www.ncbi.nlm.nih.gov/pubmed/33262889 http://dx.doi.org/10.3892/mco.2020.2171 |
_version_ | 1783614030952267776 |
---|---|
author | Hanamatsu, Yuki Saigo, Chiemi Kito, Yusuke Takeuchi, Tamotsu |
author_facet | Hanamatsu, Yuki Saigo, Chiemi Kito, Yusuke Takeuchi, Tamotsu |
author_sort | Hanamatsu, Yuki |
collection | PubMed |
description | Clear cell sarcoma (CCS) affects the deep soft tissues in young adults and is known to have high rates of metastasis, including lymphatic metastasis. In our previous study an xenoplant model of CCS was established, which exhibited local tumor growth, lymphatic metastasis, and distant metastasis in SCID-Beige mice. In the current study, the role of NK cells during metastasis in the same xenoplant murine model was investigated. Injection of murine or human NK cells significantly suppressed the metastasis of HS-MM CCS cells in SCID-Beige mice. Notably, reverse transcription-quantitative PCR analysis demonstrated that injection of NK cells did not alter the mRNA expression levels of ERSR1-ATF1, which is specifically transcribed in CCS, in the buffy coat of circulating blood cells of HS-MM-xenoplanted SCID-Beige mice. BALB/c nude mice xenoplanted with HS-MM cells exhibited local growth without evident metastasis, whereas inoculation with the anti-asialo-GM1 antibody, which has previously been found to abolish NK-cell activity, resulted in metastasis of HS-MM cells in BALB/c nude mice. The injection of the anti-CD96 antibody, which increases the cytotoxicity of NK cells, significantly suppressed the metastasis of HS-MM cells in SCID-Beige mice. These results indicated that NK cells impaired the metastatic tumor microenvironments in the present mice xenoplant model. |
format | Online Article Text |
id | pubmed-7690248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-76902482020-11-30 An obstructive role of NK cells on metastatic growth of clear-cell sarcoma cells in a xenoplant murine model Hanamatsu, Yuki Saigo, Chiemi Kito, Yusuke Takeuchi, Tamotsu Mol Clin Oncol Articles Clear cell sarcoma (CCS) affects the deep soft tissues in young adults and is known to have high rates of metastasis, including lymphatic metastasis. In our previous study an xenoplant model of CCS was established, which exhibited local tumor growth, lymphatic metastasis, and distant metastasis in SCID-Beige mice. In the current study, the role of NK cells during metastasis in the same xenoplant murine model was investigated. Injection of murine or human NK cells significantly suppressed the metastasis of HS-MM CCS cells in SCID-Beige mice. Notably, reverse transcription-quantitative PCR analysis demonstrated that injection of NK cells did not alter the mRNA expression levels of ERSR1-ATF1, which is specifically transcribed in CCS, in the buffy coat of circulating blood cells of HS-MM-xenoplanted SCID-Beige mice. BALB/c nude mice xenoplanted with HS-MM cells exhibited local growth without evident metastasis, whereas inoculation with the anti-asialo-GM1 antibody, which has previously been found to abolish NK-cell activity, resulted in metastasis of HS-MM cells in BALB/c nude mice. The injection of the anti-CD96 antibody, which increases the cytotoxicity of NK cells, significantly suppressed the metastasis of HS-MM cells in SCID-Beige mice. These results indicated that NK cells impaired the metastatic tumor microenvironments in the present mice xenoplant model. D.A. Spandidos 2021-01 2020-11-12 /pmc/articles/PMC7690248/ /pubmed/33262889 http://dx.doi.org/10.3892/mco.2020.2171 Text en Copyright: © Hanamatsu et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Hanamatsu, Yuki Saigo, Chiemi Kito, Yusuke Takeuchi, Tamotsu An obstructive role of NK cells on metastatic growth of clear-cell sarcoma cells in a xenoplant murine model |
title | An obstructive role of NK cells on metastatic growth of clear-cell sarcoma cells in a xenoplant murine model |
title_full | An obstructive role of NK cells on metastatic growth of clear-cell sarcoma cells in a xenoplant murine model |
title_fullStr | An obstructive role of NK cells on metastatic growth of clear-cell sarcoma cells in a xenoplant murine model |
title_full_unstemmed | An obstructive role of NK cells on metastatic growth of clear-cell sarcoma cells in a xenoplant murine model |
title_short | An obstructive role of NK cells on metastatic growth of clear-cell sarcoma cells in a xenoplant murine model |
title_sort | obstructive role of nk cells on metastatic growth of clear-cell sarcoma cells in a xenoplant murine model |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7690248/ https://www.ncbi.nlm.nih.gov/pubmed/33262889 http://dx.doi.org/10.3892/mco.2020.2171 |
work_keys_str_mv | AT hanamatsuyuki anobstructiveroleofnkcellsonmetastaticgrowthofclearcellsarcomacellsinaxenoplantmurinemodel AT saigochiemi anobstructiveroleofnkcellsonmetastaticgrowthofclearcellsarcomacellsinaxenoplantmurinemodel AT kitoyusuke anobstructiveroleofnkcellsonmetastaticgrowthofclearcellsarcomacellsinaxenoplantmurinemodel AT takeuchitamotsu anobstructiveroleofnkcellsonmetastaticgrowthofclearcellsarcomacellsinaxenoplantmurinemodel AT hanamatsuyuki obstructiveroleofnkcellsonmetastaticgrowthofclearcellsarcomacellsinaxenoplantmurinemodel AT saigochiemi obstructiveroleofnkcellsonmetastaticgrowthofclearcellsarcomacellsinaxenoplantmurinemodel AT kitoyusuke obstructiveroleofnkcellsonmetastaticgrowthofclearcellsarcomacellsinaxenoplantmurinemodel AT takeuchitamotsu obstructiveroleofnkcellsonmetastaticgrowthofclearcellsarcomacellsinaxenoplantmurinemodel |