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[Formula: see text] 2 [Formula: see text] 1 may be a potential marker for cancer stem cell in laryngeal squamous cell carcinoma

Cancer stem cells (CSCs) have the ability to dictate tumor initiation, recurrence, and metastasis. Here, we examined the expression of a [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] in laryngeal cancer tissues and further determined the effect of [Formula: see text] 2 [Formula: se...

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Autores principales: Huang, Chaoping, Li, Yan, Zhao, Wei, Zhang, Aobo, Lu, Cheng, Wang, Zhenxiao, Liu, Liangfa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398553/
https://www.ncbi.nlm.nih.gov/pubmed/30475757
http://dx.doi.org/10.3233/CBM-181947
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author Huang, Chaoping
Li, Yan
Zhao, Wei
Zhang, Aobo
Lu, Cheng
Wang, Zhenxiao
Liu, Liangfa
author_facet Huang, Chaoping
Li, Yan
Zhao, Wei
Zhang, Aobo
Lu, Cheng
Wang, Zhenxiao
Liu, Liangfa
author_sort Huang, Chaoping
collection PubMed
description Cancer stem cells (CSCs) have the ability to dictate tumor initiation, recurrence, and metastasis. Here, we examined the expression of a [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] in laryngeal cancer tissues and further determined the effect of [Formula: see text] 2 [Formula: see text] 1 on the migratory ability and tumorigenicity of laryngeal cancer cells. Immunofluorescence staining revealed that [Formula: see text] 2 [Formula: see text] 1 was positive in 13 (13/16, 81.25%) cases in laryngeal squamous cell carcinoma (LSCC) tissues, 7 (7/16, 43.75%) cases in paracancerous tissues and only 2 (2/16, 12.5%) cases in normal tumor tissues. Our quantitative RT-PCR assays further showed that [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] LSCC cells expressed significantly higher levels of stem cell-associated genes and drug efflux and resistance genes versus [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] cells. Sphere-forming assays demonstrated higher sphere-forming efficiency in the [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] versus [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] subpopulation. Our Matrigel assays showed that [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] cells exhibited significantly greater invasive and migratory ability than [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] cells. Furthermore, the percentage of purified [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] in TU686 and TU212 cells treated cisplatin or paclitaxel was significantly higher than that of the control group. Tumor xenograft assays revealed that the tumorigenicity of [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] cells was much higher than [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] cells. In conclusion, a [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] subpopulation with CSC-like property was present in laryngeal cancer and possessed high self-renewal activity and was sufficient for tumor growth, differentiation, migration, invasion, and chemotherapeutic resistance. They could represent a promising therapeutic target for LSCC.
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spelling pubmed-63985532019-03-06 [Formula: see text] 2 [Formula: see text] 1 may be a potential marker for cancer stem cell in laryngeal squamous cell carcinoma Huang, Chaoping Li, Yan Zhao, Wei Zhang, Aobo Lu, Cheng Wang, Zhenxiao Liu, Liangfa Cancer Biomark Research Article Cancer stem cells (CSCs) have the ability to dictate tumor initiation, recurrence, and metastasis. Here, we examined the expression of a [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] in laryngeal cancer tissues and further determined the effect of [Formula: see text] 2 [Formula: see text] 1 on the migratory ability and tumorigenicity of laryngeal cancer cells. Immunofluorescence staining revealed that [Formula: see text] 2 [Formula: see text] 1 was positive in 13 (13/16, 81.25%) cases in laryngeal squamous cell carcinoma (LSCC) tissues, 7 (7/16, 43.75%) cases in paracancerous tissues and only 2 (2/16, 12.5%) cases in normal tumor tissues. Our quantitative RT-PCR assays further showed that [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] LSCC cells expressed significantly higher levels of stem cell-associated genes and drug efflux and resistance genes versus [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] cells. Sphere-forming assays demonstrated higher sphere-forming efficiency in the [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] versus [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] subpopulation. Our Matrigel assays showed that [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] cells exhibited significantly greater invasive and migratory ability than [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] cells. Furthermore, the percentage of purified [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] in TU686 and TU212 cells treated cisplatin or paclitaxel was significantly higher than that of the control group. Tumor xenograft assays revealed that the tumorigenicity of [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] cells was much higher than [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] cells. In conclusion, a [Formula: see text] 2 [Formula: see text] 1 [Formula: see text] subpopulation with CSC-like property was present in laryngeal cancer and possessed high self-renewal activity and was sufficient for tumor growth, differentiation, migration, invasion, and chemotherapeutic resistance. They could represent a promising therapeutic target for LSCC. IOS Press 2019-02-20 /pmc/articles/PMC6398553/ /pubmed/30475757 http://dx.doi.org/10.3233/CBM-181947 Text en © 2019 – IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This article is published online with Open Access and distributed under the terms of the Creative Commons Attribution Non-Commercial License (CC BY-NC 4.0).
spellingShingle Research Article
Huang, Chaoping
Li, Yan
Zhao, Wei
Zhang, Aobo
Lu, Cheng
Wang, Zhenxiao
Liu, Liangfa
[Formula: see text] 2 [Formula: see text] 1 may be a potential marker for cancer stem cell in laryngeal squamous cell carcinoma
title [Formula: see text] 2 [Formula: see text] 1 may be a potential marker for cancer stem cell in laryngeal squamous cell carcinoma
title_full [Formula: see text] 2 [Formula: see text] 1 may be a potential marker for cancer stem cell in laryngeal squamous cell carcinoma
title_fullStr [Formula: see text] 2 [Formula: see text] 1 may be a potential marker for cancer stem cell in laryngeal squamous cell carcinoma
title_full_unstemmed [Formula: see text] 2 [Formula: see text] 1 may be a potential marker for cancer stem cell in laryngeal squamous cell carcinoma
title_short [Formula: see text] 2 [Formula: see text] 1 may be a potential marker for cancer stem cell in laryngeal squamous cell carcinoma
title_sort [formula: see text] 2 [formula: see text] 1 may be a potential marker for cancer stem cell in laryngeal squamous cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6398553/
https://www.ncbi.nlm.nih.gov/pubmed/30475757
http://dx.doi.org/10.3233/CBM-181947
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