STAT3 promotes chronic lymphocytic leukemia progression through upregulating SMYD3 expression

Wei Ma, Yingying Zhang, Yu Qi, Shi-dong Guo
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引用次数: 4

Abstract

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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STAT3通过上调SMYD3表达促进慢性淋巴细胞白血病的进展
本研究旨在探讨STAT3和SMYD3在慢性淋巴细胞白血病中的作用,以及STAT3和SMYD3在慢性淋巴细胞白血病中的调控关系。材料与方法采用RT-qPCR和western blot检测慢性淋巴细胞白血病(MEC1、CLL)标本和细胞中STAT3和SMYD3的表达。利用小干扰RNA敲低STAT3 mRNA水平,利用pcDNA3.1-SMYD3质粒构建SMYD3过表达模型。MTT法测定细胞增殖情况。transwell法检测细胞侵袭能力。随后,采用荧光素酶报告基因实验和染色质免疫沉淀实验(ChIP)证实STAT3与SMYD3之间的相关性。结果STAT3在慢性淋巴细胞白血病单核细胞和癌细胞中高表达。STAT3敲低可显著抑制MEC1和CLL细胞系中SMYD3 mRNA和蛋白的表达。荧光素酶报告基因实验结合ChIP实验发现STAT3与STAT3的启动子区域结合,参与SMYD3的转录。STAT3的下调与抑制细胞增殖和侵袭能力呈正相关,而SMYD3的过表达与抑制细胞增殖和侵袭能力呈负相关。结论STAT3可能通过提高SMYD3的表达促进慢性淋巴细胞白血病的进展。靶向STAT3和SMYD3可能是慢性淋巴细胞白血病的潜在治疗策略。
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