Linc01588 deletion inhibits the malignant biological characteristics of hydroquinone-induced leukemic cells via miR-9-5p/SIRT1

• Published in: Ecotoxicology and environmental safety Vol. 276; p. 116295
• Main Authors: Liu, Yanquan, Zeng, Minjuan, Li, Zhengzhen, Lin, Caixiong, Bao, Jie, Ding, Weihua, Wang, Shimei, Fan, Qin, Sun, Qian, Luo, Hao, Huang, Jinqi, Chen, Shaopeng, Tang, Huanwen
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier Inc 01-05-2024; Elsevier
• Subjects: Hydroquinone; Leukemia; Linc01588; Malignant biological characteristics; miR-9-5p/SIRT1 axis; Hydroquinone; miR-9-5p/SIRT1 axis; Malignant biological characteristics; Leukemia; Linc01588
• ISSN: 0147-6513; 1090-2414
• DOI: 10.1016/j.ecoenv.2024.116295

Leukemia caused by environmental chemical pollutants has attracted great attention, the malignant leukemic transformation model of TK6 cells induced by hydroquinone (HQ) has been previously found in our team. However, the type of leukemia corresponding to this malignant transformed cell line model needs further study and interpretation. Furthermore, the molecular mechanism of malignant proliferation of leukemic cells induced by HQ remains unclear. This study is the first to reveal the expression of aberrant genes in leukemic cells of HQ-induced malignant transformation, which may correspond to chronic lymphocytic leukemia (CLL). The expression of Linc01588, a long non-coding RNA (lncRNA), was significantly up-regulated in CLL patients and leukemic cell line model which previously described. After gain-of-function assays and loss-of-function assays, feeble cell viability, severe apoptotic phenotype and the increased secretion of TNF-α were easily observed in malignant leukemic TK6 cells with Linc01588 deletion after HQ intervention. The tumors derived from malignant TK6 cells with Linc01588 deletion inoculated subcutaneously in nude mice were smaller than controls. In CLL and its cell line model, the expression of Linc01588 and miR-9–5p, miR-9–5p and SIRT1 were negative correlation respectively in CLL and cell line model, while the expression of Linc01588 and SIRT1 were positive correlation. The dual-luciferase reporter assay showed that Linc01588 & miR-9–5p, miR-9–5p & SIRT1 could bind directly, respectively. Furthermore, knockdown of miR-9–5p successfully rescued the severe apoptotic phenotype and the increased secretion of TNF-α caused by the Linc01588 deletion, the deletion of Linc01588 in human CLL cell line MEC-2 could also inhibit malignant biological characteristics, and the phenotype caused by the deletion of Linc01588 could also be rescued after overexpression of SIRT1. Moreover, the regulation of SIRT1 expression in HQ19 cells by Linc01588 and miR-9–5 P may be related to the Akt/NF-κB pathway. In brief, Linc01588 deletion inhibits the malignant biological characteristics of HQ-induced leukemic cells via miR-9–5p/SIRT1, and it is a novel and hopeful clue for the clinical targeted therapy of CLL.
•HQ-induced leukemic cells may also correspond to chronic lymphocytic leukemia (CLL).•Knockdown of miR-9–5p rescued the malignant phenotype caused by Linc01588 deletion.•Overexpression of SIRT1 triggers malignant phenotype caused by deletion of Linc01588.•Linc01588 deletion inhibits malignant features via miR-9–5p/SIRT1 axis.•Targeting Linc01588 or miR-9–5p may be a new clue for the treatment of CLL.