Promoting effects of calponin 3 on the growth of diffuse large B-cell lymphoma cells

被引:1
作者
Xing, Xiaojing [1 ,4 ]
Liu, Meichen [1 ]
Wang, Xuguang [2 ]
Guo, Qianxue [1 ]
Wang, Hongyue [3 ]
机构
[1] Dalian Univ Technol, Canc Hosp, Dept Hematol & Breast Canc, Liaoning Canc Hosp & Inst, Shenyang 110042, Liaoning, Peoples R China
[2] Shenyang Med Coll, Dept Pathol, Shenyang 110034, Liaoning, Peoples R China
[3] Dalian Univ Technol, Canc Hosp, Liaoning Canc Hosp & Inst, Dept Sci Res & Acad, Shenyang 110042, Liaoning, Peoples R China
[4] Dalian Univ Technol, Canc Hosp, Liaoning Canc Hosp & Inst, Dept Hematol & Breast Canc, 44 Xiaoheyan Rd, Shenyang 110042, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
diffuse large B-cell lymphoma; calponin; 3; forkhead box O3; proliferation; apoptosis; GENE-EXPRESSION; SMOOTH-MUSCLE; CANCER; APOPTOSIS; FOXO3A; DEATH; CYCLE;
D O I
10.3892/or.2023.8483
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Diffuse large B-cell lymphoma (DLBCL) is one of the most common types of lymphoma. Calponin 3 (CNN3) is a thin filament-associated protein previously known to regulate smooth muscle contraction. Recent evidence illustrates its involvement in carcinogenesis; however, its roles in DLBCL remain unknown. CNN3 was found to be highly expressed in DLBCL specimens according to the online Gene Expression Profiling Interactive Analysis data. The aim of the present study was to investigate the roles of CNN3 in the progression of DLBCL. In vitro, the ectopic expression of CNN3 promoted the proliferation and G1/S transition of DLBCL cells, while its silencing led to opposite alterations. A similar tumor-promoting role of CNN3 was also demonstrated by injecting nude mice with DLBCL cells over- or underexpressing CNN3. The results of dual-luciferase reporter and chromatin immunoprecipitation assays revealed that forkhead box O3 (FOXO3), a known tumor suppressor in DLBCL, bound to the CNN3 promoter at -1955/-1948 and -1190/-1183, and suppressed the transcription of CNN3. The alterations induced by FOXO3 were partly blocked by CNN3 overexpression. On the whole, the present study demonstrates that CNN3, whose transcriptional activity is negatively regulated by FOXO3, contributes to the malignant behavior of DLBCL cells. The findings of the present study may provide novel diagnostic or therapeutic insight for DLBCL in clinical practice.
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页数:14
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