LncRNA ABHD11-AS1 Elevates CALM2 to Promote Metastasis of Thyroid Cancer Through Sponging miR-876-5p.

IF 1.6 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochemical Genetics Pub Date : 2025-03-21 DOI:10.1007/s10528-025-11072-9
Juan Lv, Fukun Chen, Ling Lv, Lu Zhang, Huangren Zou, Yanlin Liu, Yuke Bai, Ruotong Fang, Tiantian Qin, Zhiyong Deng
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Abstract

In the past decade, the treatment of thyroid cancer (TC) has been brought to a new era, but tumor metastasis still is an intractable difficulty in clinical. LncRNA ABHD11-AS1 has been confirmed to be involved in TC progression. However, its specific mechanism remains unknown. Tissues from TC patients and TC cells served as mainly experimental subjects in this study. The migration of TC cells was assessed using the scratch assay, and the ability of cell invasion was evaluated by transwell assay. RT-qPCR and western blot were conducted to determine the levels of related genes and proteins. The dual-luciferase reporter assay was used to validate the relationships among ABHD11-AS1, miR-876-5p and CALM2. ABHD11-AS1 and CALM2 are elevated in TC cancer samples and cells, while the expression of miR-876-5p is reduced. Subsequently, the ability of TC cells to migrate, invade and EMT was inhibited by both ABHD11-AS1 knockdown or miR-876-5p overexpression. Moreover, the suppression of malignant characteristics in TC cells resulting from ABHD11-AS knockdown was counteracted by the inhibition of miR-876-5p or the upregulation of CALM2. On the mechanism, ABHD11-AS1 elevated CALM2 and promoted the malignant development of TC cells by acting as a miR-876-5p sponge. ABHD11-AS1 mediated the miR-876-5p/CALM2 axis to drive the metastasis of thyroid cancer.

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LncRNA ABHD11-AS1通过海绵miR-876-5p上调CALM2促进甲状腺癌转移
近十年来,甲状腺癌(TC)的治疗进入了一个新的时代,但肿瘤转移仍然是临床难以解决的难题。LncRNA ABHD11-AS1已被证实参与TC进展。然而,其具体机制尚不清楚。本研究以TC患者组织和TC细胞为主要实验对象。采用划痕法评估TC细胞的迁移能力,transwell法评估细胞的侵袭能力。RT-qPCR和western blot检测相关基因和蛋白的表达水平。采用双荧光素酶报告试验验证ABHD11-AS1、miR-876-5p和CALM2之间的关系。ABHD11-AS1和CALM2在TC癌样本和细胞中表达升高,miR-876-5p表达降低。随后,ABHD11-AS1敲低或miR-876-5p过表达均抑制TC细胞迁移、侵袭和EMT的能力。此外,ABHD11-AS敲低对TC细胞恶性特征的抑制被miR-876-5p的抑制或CALM2的上调所抵消。在机制上,ABHD11-AS1通过作为miR-876-5p海绵,升高CALM2,促进TC细胞恶性发展。ABHD11-AS1介导miR-876-5p/CALM2轴驱动甲状腺癌转移。
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来源期刊
Biochemical Genetics
Biochemical Genetics 生物-生化与分子生物学
CiteScore
3.90
自引率
0.00%
发文量
133
审稿时长
4.8 months
期刊介绍: Biochemical Genetics welcomes original manuscripts that address and test clear scientific hypotheses, are directed to a broad scientific audience, and clearly contribute to the advancement of the field through the use of sound sampling or experimental design, reliable analytical methodologies and robust statistical analyses. Although studies focusing on particular regions and target organisms are welcome, it is not the journal’s goal to publish essentially descriptive studies that provide results with narrow applicability, or are based on very small samples or pseudoreplication. Rather, Biochemical Genetics welcomes review articles that go beyond summarizing previous publications and create added value through the systematic analysis and critique of the current state of knowledge or by conducting meta-analyses. Methodological articles are also within the scope of Biological Genetics, particularly when new laboratory techniques or computational approaches are fully described and thoroughly compared with the existing benchmark methods. Biochemical Genetics welcomes articles on the following topics: Genomics; Proteomics; Population genetics; Phylogenetics; Metagenomics; Microbial genetics; Genetics and evolution of wild and cultivated plants; Animal genetics and evolution; Human genetics and evolution; Genetic disorders; Genetic markers of diseases; Gene technology and therapy; Experimental and analytical methods; Statistical and computational methods.
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