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CTLA-4 promotes lymphoma progression through tumor stem cell enrichment and immunosuppression
The recurrence rate of lymphoma is very high, and tumor stem cells may be an important mechanism. Cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) can inhibit antitumor immunity and promote cancer progression, but its role and mechanism in lymphoma are still unclear. Here we collected lymphoma t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
De Gruyter
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422981/ https://www.ncbi.nlm.nih.gov/pubmed/34553071 http://dx.doi.org/10.1515/biol-2021-0094 |
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author | Chen, Yan Li, Meng Cao, Jian Cai, Guohong Li, Xiantao Liu, Yuejiao Chen, Wen |
author_facet | Chen, Yan Li, Meng Cao, Jian Cai, Guohong Li, Xiantao Liu, Yuejiao Chen, Wen |
author_sort | Chen, Yan |
collection | PubMed |
description | The recurrence rate of lymphoma is very high, and tumor stem cells may be an important mechanism. Cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) can inhibit antitumor immunity and promote cancer progression, but its role and mechanism in lymphoma are still unclear. Here we collected lymphoma tissue and peripheral blood from patients with diffuse large B-cell lymphoma (DLBCL). Results showed that CTLA-4 expression and CD44+ cell in the high-risk group were significantly higher than that in the low-risk group. Correlation analysis showed that CTLA-4 expression positively correlated with CD44+ cell in lymphoma tissue and regulatory T (Treg) cells in lymphocytes. In vitro experiment showed that CTLA-4 increased the ratio of lymphoma stem cells, and proliferation and invasion of lymphoma cells through TGF-β pathway. Moreover, CTLA-4 enhanced the proliferation of Treg cells induced by lymphoma cells. Animal experiments showed that CTLA-4 can promote transplanted lymphoma growth. Immunohistochemistry results showed that both Ki-67 and CD44+ cells increased significantly in the CTLA-4 group. TGF-β neutralization can significantly block these effects of CTLA-4. In conclusion, CTLA-4 promoted DLBCL progression through lymphoma stem cell enrichment and immunosuppression. |
format | Online Article Text |
id | pubmed-8422981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | De Gruyter |
record_format | MEDLINE/PubMed |
spelling | pubmed-84229812021-09-21 CTLA-4 promotes lymphoma progression through tumor stem cell enrichment and immunosuppression Chen, Yan Li, Meng Cao, Jian Cai, Guohong Li, Xiantao Liu, Yuejiao Chen, Wen Open Life Sci Research Article The recurrence rate of lymphoma is very high, and tumor stem cells may be an important mechanism. Cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) can inhibit antitumor immunity and promote cancer progression, but its role and mechanism in lymphoma are still unclear. Here we collected lymphoma tissue and peripheral blood from patients with diffuse large B-cell lymphoma (DLBCL). Results showed that CTLA-4 expression and CD44+ cell in the high-risk group were significantly higher than that in the low-risk group. Correlation analysis showed that CTLA-4 expression positively correlated with CD44+ cell in lymphoma tissue and regulatory T (Treg) cells in lymphocytes. In vitro experiment showed that CTLA-4 increased the ratio of lymphoma stem cells, and proliferation and invasion of lymphoma cells through TGF-β pathway. Moreover, CTLA-4 enhanced the proliferation of Treg cells induced by lymphoma cells. Animal experiments showed that CTLA-4 can promote transplanted lymphoma growth. Immunohistochemistry results showed that both Ki-67 and CD44+ cells increased significantly in the CTLA-4 group. TGF-β neutralization can significantly block these effects of CTLA-4. In conclusion, CTLA-4 promoted DLBCL progression through lymphoma stem cell enrichment and immunosuppression. De Gruyter 2021-09-06 /pmc/articles/PMC8422981/ /pubmed/34553071 http://dx.doi.org/10.1515/biol-2021-0094 Text en © 2021 Yan Chen et al., published by De Gruyter https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. |
spellingShingle | Research Article Chen, Yan Li, Meng Cao, Jian Cai, Guohong Li, Xiantao Liu, Yuejiao Chen, Wen CTLA-4 promotes lymphoma progression through tumor stem cell enrichment and immunosuppression |
title | CTLA-4 promotes lymphoma progression through tumor stem cell enrichment and immunosuppression |
title_full | CTLA-4 promotes lymphoma progression through tumor stem cell enrichment and immunosuppression |
title_fullStr | CTLA-4 promotes lymphoma progression through tumor stem cell enrichment and immunosuppression |
title_full_unstemmed | CTLA-4 promotes lymphoma progression through tumor stem cell enrichment and immunosuppression |
title_short | CTLA-4 promotes lymphoma progression through tumor stem cell enrichment and immunosuppression |
title_sort | ctla-4 promotes lymphoma progression through tumor stem cell enrichment and immunosuppression |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422981/ https://www.ncbi.nlm.nih.gov/pubmed/34553071 http://dx.doi.org/10.1515/biol-2021-0094 |
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