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STAT3 promotes chronic lymphocytic leukemia progression through upregulating SMYD3 expression

INTRODUCTION: This study was designed to investigate the roles of STAT3 and SMYD3 in chronic lymphocytic leukemia and the regulatory relationship between STAT3 and SMYD3 in chronic lymphocytic leukemia. MATERIAL AND METHODS: The expression of STAT3 and SMYD3 was determined by RT-qPCR and western blo...

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Autores principales: Ma, Wei, Zhang, Yingying, Qi, Yu, Guo, Shidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764298/
https://www.ncbi.nlm.nih.gov/pubmed/31572461
http://dx.doi.org/10.5114/aoms.2018.77733
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author Ma, Wei
Zhang, Yingying
Qi, Yu
Guo, Shidong
author_facet Ma, Wei
Zhang, Yingying
Qi, Yu
Guo, Shidong
author_sort Ma, Wei
collection PubMed
description INTRODUCTION: This study was designed to investigate the roles of STAT3 and SMYD3 in chronic lymphocytic leukemia and the regulatory relationship between STAT3 and SMYD3 in chronic lymphocytic leukemia. MATERIAL AND METHODS: The expression of STAT3 and SMYD3 was determined by RT-qPCR and western blot in chronic lymphocytic leukemia samples and cells (MEC1, CLL). Small interfering RNA was used to knock down the mRNA level of STAT3 and the pcDNA3.1-SMYD3 plasmid was used to construct a SMYD3 overexpression model. An MTT assay was performed to evaluate cell proliferation. A transwell assay was used to detect cell invasion ability. Afterwards, a luciferase reporter assay and chromatin immunoprecipitation experiment (ChIP assay) were applied to confirm the correlation between STAT3 and SMYD3. RESULTS: STAT3 was highly expressed in chronic lymphocytic leukemia mononuclear cells and cancerous cell lines. STAT3 knockdown dramatically inhibited the mRNA and protein expression of SMYD3 in MEC1 and CLL cell lines. The luciferase reporter assay combined with the ChIP assay revealed that STAT3 bound to the promoter region of STAT3 and contributed to the transcription of SMYD3. Knockdown of STAT3 positively correlated with inhibition of cell proliferation and invasion abilities, while overexpression of SMYD3 negatively correlated with inhibition of cell proliferation and invasion. CONCLUSIONS: STAT3 may promote chronic lymphocytic leukemia progression through elevating SMYD3 expression. Targeting STAT3 and SMYD3 may be a potential therapeutic strategy for chronic lymphocytic leukemia.
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spelling pubmed-67642982019-09-30 STAT3 promotes chronic lymphocytic leukemia progression through upregulating SMYD3 expression Ma, Wei Zhang, Yingying Qi, Yu Guo, Shidong Arch Med Sci Basic Research INTRODUCTION: This study was designed to investigate the roles of STAT3 and SMYD3 in chronic lymphocytic leukemia and the regulatory relationship between STAT3 and SMYD3 in chronic lymphocytic leukemia. MATERIAL AND METHODS: The expression of STAT3 and SMYD3 was determined by RT-qPCR and western blot in chronic lymphocytic leukemia samples and cells (MEC1, CLL). Small interfering RNA was used to knock down the mRNA level of STAT3 and the pcDNA3.1-SMYD3 plasmid was used to construct a SMYD3 overexpression model. An MTT assay was performed to evaluate cell proliferation. A transwell assay was used to detect cell invasion ability. Afterwards, a luciferase reporter assay and chromatin immunoprecipitation experiment (ChIP assay) were applied to confirm the correlation between STAT3 and SMYD3. RESULTS: STAT3 was highly expressed in chronic lymphocytic leukemia mononuclear cells and cancerous cell lines. STAT3 knockdown dramatically inhibited the mRNA and protein expression of SMYD3 in MEC1 and CLL cell lines. The luciferase reporter assay combined with the ChIP assay revealed that STAT3 bound to the promoter region of STAT3 and contributed to the transcription of SMYD3. Knockdown of STAT3 positively correlated with inhibition of cell proliferation and invasion abilities, while overexpression of SMYD3 negatively correlated with inhibition of cell proliferation and invasion. CONCLUSIONS: STAT3 may promote chronic lymphocytic leukemia progression through elevating SMYD3 expression. Targeting STAT3 and SMYD3 may be a potential therapeutic strategy for chronic lymphocytic leukemia. Termedia Publishing House 2018-08-23 2019-09 /pmc/articles/PMC6764298/ /pubmed/31572461 http://dx.doi.org/10.5114/aoms.2018.77733 Text en Copyright: © 2018 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Basic Research
Ma, Wei
Zhang, Yingying
Qi, Yu
Guo, Shidong
STAT3 promotes chronic lymphocytic leukemia progression through upregulating SMYD3 expression
title STAT3 promotes chronic lymphocytic leukemia progression through upregulating SMYD3 expression
title_full STAT3 promotes chronic lymphocytic leukemia progression through upregulating SMYD3 expression
title_fullStr STAT3 promotes chronic lymphocytic leukemia progression through upregulating SMYD3 expression
title_full_unstemmed STAT3 promotes chronic lymphocytic leukemia progression through upregulating SMYD3 expression
title_short STAT3 promotes chronic lymphocytic leukemia progression through upregulating SMYD3 expression
title_sort stat3 promotes chronic lymphocytic leukemia progression through upregulating smyd3 expression
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764298/
https://www.ncbi.nlm.nih.gov/pubmed/31572461
http://dx.doi.org/10.5114/aoms.2018.77733
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