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Effect of hematopoietic progenitor cells on the biological characteristics of colon cancer tumor stem cells
BACKGROUND: Cancer stem cells (CSCs) are a type of tumor cell that are self-sustaining and can differentiate into several different types of cells. The present study aims to investigate the effect of hematopoietic progenitor cells (HPCs) on the biological behavior of colon CSCs (CCSCs) and to determ...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797965/ https://www.ncbi.nlm.nih.gov/pubmed/35116403 http://dx.doi.org/10.21037/tcr-20-2810 |
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author | Guan, Shen Yang, Chunkang Wu, Lihuo |
author_facet | Guan, Shen Yang, Chunkang Wu, Lihuo |
author_sort | Guan, Shen |
collection | PubMed |
description | BACKGROUND: Cancer stem cells (CSCs) are a type of tumor cell that are self-sustaining and can differentiate into several different types of cells. The present study aims to investigate the effect of hematopoietic progenitor cells (HPCs) on the biological behavior of colon CSCs (CCSCs) and to determine the underlying molecular mechanisms of liver metastasis in colorectal cancer. METHODS: Subsets of CCSCs were isolated from stem-like HCT116 cells and cocultured with CD133(+) HPCs in vitro. Colony formation assay, and CCK-8 were used to assess the effects of HPCs on CCSC subsets. Invasive and migration assay were done to study the effects of HPCs mediated metastatic capacity of CCSC subsets. Expression of MMP-9, VEGF, E-cadherin and β-catenin was analyzed by qPCR and Western blotting. RESULTS: CCK-8 and colony formation assays showed that HPCs significantly promoted proliferation and colony formation of the CCSC subsets (P=0.031). HPCs also significantly enhanced the migration (P=0.011) and invasive capacity (P=0.001) of the CCSC subsets. Quantitative PCR showed that MMP-9 and VEGF expression in CCSC subsets were significantly upregulated (P=0.000 and P=0.005). Western blotting showed that MMP-9, VEGF and β-catenin expression in CCSC subsets were significantly upregulated (P=0.000, P=0.005, P=0.000). The protein expression levels of E-cadherin in the CCSC subsets was significantly downregulated (P=0.002). CONCLUSIONS: CD133(+) HPCs enhanced migration, invasion and proliferation of CCSC subsets in vitro. |
format | Online Article Text |
id | pubmed-8797965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-87979652022-02-02 Effect of hematopoietic progenitor cells on the biological characteristics of colon cancer tumor stem cells Guan, Shen Yang, Chunkang Wu, Lihuo Transl Cancer Res Original Article BACKGROUND: Cancer stem cells (CSCs) are a type of tumor cell that are self-sustaining and can differentiate into several different types of cells. The present study aims to investigate the effect of hematopoietic progenitor cells (HPCs) on the biological behavior of colon CSCs (CCSCs) and to determine the underlying molecular mechanisms of liver metastasis in colorectal cancer. METHODS: Subsets of CCSCs were isolated from stem-like HCT116 cells and cocultured with CD133(+) HPCs in vitro. Colony formation assay, and CCK-8 were used to assess the effects of HPCs on CCSC subsets. Invasive and migration assay were done to study the effects of HPCs mediated metastatic capacity of CCSC subsets. Expression of MMP-9, VEGF, E-cadherin and β-catenin was analyzed by qPCR and Western blotting. RESULTS: CCK-8 and colony formation assays showed that HPCs significantly promoted proliferation and colony formation of the CCSC subsets (P=0.031). HPCs also significantly enhanced the migration (P=0.011) and invasive capacity (P=0.001) of the CCSC subsets. Quantitative PCR showed that MMP-9 and VEGF expression in CCSC subsets were significantly upregulated (P=0.000 and P=0.005). Western blotting showed that MMP-9, VEGF and β-catenin expression in CCSC subsets were significantly upregulated (P=0.000, P=0.005, P=0.000). The protein expression levels of E-cadherin in the CCSC subsets was significantly downregulated (P=0.002). CONCLUSIONS: CD133(+) HPCs enhanced migration, invasion and proliferation of CCSC subsets in vitro. AME Publishing Company 2021-02 /pmc/articles/PMC8797965/ /pubmed/35116403 http://dx.doi.org/10.21037/tcr-20-2810 Text en 2021 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Original Article Guan, Shen Yang, Chunkang Wu, Lihuo Effect of hematopoietic progenitor cells on the biological characteristics of colon cancer tumor stem cells |
title | Effect of hematopoietic progenitor cells on the biological characteristics of colon cancer tumor stem cells |
title_full | Effect of hematopoietic progenitor cells on the biological characteristics of colon cancer tumor stem cells |
title_fullStr | Effect of hematopoietic progenitor cells on the biological characteristics of colon cancer tumor stem cells |
title_full_unstemmed | Effect of hematopoietic progenitor cells on the biological characteristics of colon cancer tumor stem cells |
title_short | Effect of hematopoietic progenitor cells on the biological characteristics of colon cancer tumor stem cells |
title_sort | effect of hematopoietic progenitor cells on the biological characteristics of colon cancer tumor stem cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8797965/ https://www.ncbi.nlm.nih.gov/pubmed/35116403 http://dx.doi.org/10.21037/tcr-20-2810 |
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