Cargando…

OVOL2 links stemness and metastasis via fine-tuning epithelial-mesenchymal transition in nasopharyngeal carcinoma

Rationale: Metastasis is the leading cause of disease-related death among patients with nasopharyngeal carcinoma (NPC). Mounting evidence suggest that epithelial-mesenchymal transition (EMT) is crucial for cancer cells to acquire metastatic ability. In this study, we aim to clarify the extent to whi...

Descripción completa

Detalles Bibliográficos
Autores principales: Qi, Xue-Kang, Han, Hui-Qiong, Zhang, Hao-Jiong, Xu, Miao, Li, Lili, Chen, Lin, Xiang, Tong, Feng, Qi-Sheng, Kang, Tiebang, Qian, Chao-Nan, Cai, Mu-Yan, Tao, Qian, Zeng, Yi-Xin, Feng, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928881/
https://www.ncbi.nlm.nih.gov/pubmed/29721073
http://dx.doi.org/10.7150/thno.24003
_version_ 1783319313323655168
author Qi, Xue-Kang
Han, Hui-Qiong
Zhang, Hao-Jiong
Xu, Miao
Li, Lili
Chen, Lin
Xiang, Tong
Feng, Qi-Sheng
Kang, Tiebang
Qian, Chao-Nan
Cai, Mu-Yan
Tao, Qian
Zeng, Yi-Xin
Feng, Lin
author_facet Qi, Xue-Kang
Han, Hui-Qiong
Zhang, Hao-Jiong
Xu, Miao
Li, Lili
Chen, Lin
Xiang, Tong
Feng, Qi-Sheng
Kang, Tiebang
Qian, Chao-Nan
Cai, Mu-Yan
Tao, Qian
Zeng, Yi-Xin
Feng, Lin
author_sort Qi, Xue-Kang
collection PubMed
description Rationale: Metastasis is the leading cause of disease-related death among patients with nasopharyngeal carcinoma (NPC). Mounting evidence suggest that epithelial-mesenchymal transition (EMT) is crucial for cancer cells to acquire metastatic ability. In this study, we aim to clarify the extent to which EMT is involved in various cancer properties and identify novel markers for predicting the prognosis of NPC patients. Methods: Two cellular models derived from the same NPC cell line with distinct metastasis ability were used for microarray analysis to identify key transcriptional factors that drive metastasis. Cell migration and invasion were analyzed by wound healing and Transwell analysis. Lung metatasis was determined by tail vein injection assay. Cancer stemness was analyzed using colony formation and xenograft assay. The EMT extent was evaluated using immunoblotting, RT-qPCR and immunofluorescence of EMT markers. The value of OVOL2 in prognosis was determined by immunohistochemistry in NPC biopsies. Results: OVOL2 was the most significantly down-regulated EMT transcription factor (EMT-TF) in cellular models of NPC metatasis. Low levels of OVOL2 were associated with poor overall survival of NPC patients and the reduced expression is partly due to promoter methylation and epithelial dedifferentiation. Knockout of OVOL2 in epithelial-like NPC cells partially activates EMT program and significantly promotes cancer stemness and metastatic phenotypes. Conversely, ectopically expression of OVOL2 in mesenchymal-like cells leads to a partial transition to an epithelial phenotype and reduced malignancy. Reversing EMT by depleting ZEB1, a major target of OVOL2, does not eliminate the stemness advantage of OVOL2-deficient cells but does reduce their invasion capacity. A comparison of subpopulations at different stages of EMT revealed that the extent of EMT is positively correlated with metastasis and drug resistance; however, only the intermediate EMT state is associated with cancer stemness. Conclusion: Distinct from other canonical EMT-TFs, OVOL2 only exhibits modest effect on EMT but has a strong impact on both metastasis and tumorigenesis. Therefore, OVOL2 could serve as a prognostic indicator for cancer patients.
format Online
Article
Text
id pubmed-5928881
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-59288812018-05-02 OVOL2 links stemness and metastasis via fine-tuning epithelial-mesenchymal transition in nasopharyngeal carcinoma Qi, Xue-Kang Han, Hui-Qiong Zhang, Hao-Jiong Xu, Miao Li, Lili Chen, Lin Xiang, Tong Feng, Qi-Sheng Kang, Tiebang Qian, Chao-Nan Cai, Mu-Yan Tao, Qian Zeng, Yi-Xin Feng, Lin Theranostics Research Paper Rationale: Metastasis is the leading cause of disease-related death among patients with nasopharyngeal carcinoma (NPC). Mounting evidence suggest that epithelial-mesenchymal transition (EMT) is crucial for cancer cells to acquire metastatic ability. In this study, we aim to clarify the extent to which EMT is involved in various cancer properties and identify novel markers for predicting the prognosis of NPC patients. Methods: Two cellular models derived from the same NPC cell line with distinct metastasis ability were used for microarray analysis to identify key transcriptional factors that drive metastasis. Cell migration and invasion were analyzed by wound healing and Transwell analysis. Lung metatasis was determined by tail vein injection assay. Cancer stemness was analyzed using colony formation and xenograft assay. The EMT extent was evaluated using immunoblotting, RT-qPCR and immunofluorescence of EMT markers. The value of OVOL2 in prognosis was determined by immunohistochemistry in NPC biopsies. Results: OVOL2 was the most significantly down-regulated EMT transcription factor (EMT-TF) in cellular models of NPC metatasis. Low levels of OVOL2 were associated with poor overall survival of NPC patients and the reduced expression is partly due to promoter methylation and epithelial dedifferentiation. Knockout of OVOL2 in epithelial-like NPC cells partially activates EMT program and significantly promotes cancer stemness and metastatic phenotypes. Conversely, ectopically expression of OVOL2 in mesenchymal-like cells leads to a partial transition to an epithelial phenotype and reduced malignancy. Reversing EMT by depleting ZEB1, a major target of OVOL2, does not eliminate the stemness advantage of OVOL2-deficient cells but does reduce their invasion capacity. A comparison of subpopulations at different stages of EMT revealed that the extent of EMT is positively correlated with metastasis and drug resistance; however, only the intermediate EMT state is associated with cancer stemness. Conclusion: Distinct from other canonical EMT-TFs, OVOL2 only exhibits modest effect on EMT but has a strong impact on both metastasis and tumorigenesis. Therefore, OVOL2 could serve as a prognostic indicator for cancer patients. Ivyspring International Publisher 2018-03-08 /pmc/articles/PMC5928881/ /pubmed/29721073 http://dx.doi.org/10.7150/thno.24003 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Qi, Xue-Kang
Han, Hui-Qiong
Zhang, Hao-Jiong
Xu, Miao
Li, Lili
Chen, Lin
Xiang, Tong
Feng, Qi-Sheng
Kang, Tiebang
Qian, Chao-Nan
Cai, Mu-Yan
Tao, Qian
Zeng, Yi-Xin
Feng, Lin
OVOL2 links stemness and metastasis via fine-tuning epithelial-mesenchymal transition in nasopharyngeal carcinoma
title OVOL2 links stemness and metastasis via fine-tuning epithelial-mesenchymal transition in nasopharyngeal carcinoma
title_full OVOL2 links stemness and metastasis via fine-tuning epithelial-mesenchymal transition in nasopharyngeal carcinoma
title_fullStr OVOL2 links stemness and metastasis via fine-tuning epithelial-mesenchymal transition in nasopharyngeal carcinoma
title_full_unstemmed OVOL2 links stemness and metastasis via fine-tuning epithelial-mesenchymal transition in nasopharyngeal carcinoma
title_short OVOL2 links stemness and metastasis via fine-tuning epithelial-mesenchymal transition in nasopharyngeal carcinoma
title_sort ovol2 links stemness and metastasis via fine-tuning epithelial-mesenchymal transition in nasopharyngeal carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928881/
https://www.ncbi.nlm.nih.gov/pubmed/29721073
http://dx.doi.org/10.7150/thno.24003
work_keys_str_mv AT qixuekang ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT hanhuiqiong ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT zhanghaojiong ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT xumiao ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT lilili ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT chenlin ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT xiangtong ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT fengqisheng ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT kangtiebang ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT qianchaonan ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT caimuyan ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT taoqian ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT zengyixin ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma
AT fenglin ovol2linksstemnessandmetastasisviafinetuningepithelialmesenchymaltransitioninnasopharyngealcarcinoma