CORO1C Regulates the Malignant Biological Behavior of Ovarian Cancer Cells and Modulates the mRNA Expression Profile through the PI3K/AKT Signaling Pathway.

IF 1.8 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Cell Biochemistry and Biophysics Pub Date : 2024-10-21 DOI:10.1007/s12013-024-01591-4
Na Lu, Yongfeng Guo, Lixin Ren, Hongwei Zhao, Lijun Yan, Haiqiong Han, Sanyuan Zhang
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Abstract

Ovarian cancer (OC) is a frequently occurring gynecological tumor, and its global incidence has recently increased. Coronin-like actin-binding protein 1C (CORO1C) is known to activate the phosphoinositide 3-kinase (PI3K)-protein kinase B (AKT) pathway and promote tumor progression. However, its role in OC remains unclear. This study investigated the role of CORO1C in OC malignancy. In this study, quantitative real-time polymerase chain reaction (qRT-PCR) was used to examine AKT and CORO1C mRNA expression in clinical OC tissues and cells. Immunohistochemical analysis and western blotting were used to examine protein expression in OC tissues and cells, respectively. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), scratch wound-healing, and Transwell assays were performed to examine cell proliferation and migration. RNA-Seq was used to validate the relationship between AKT and CORO1C expression. The results showed that CORO1C was highly expressed in clinical OC tissues and SKOV3 cells, correlating with the International Federation of Gynecology and Obstetrics (FIGO) stage. Furthermore, CORO1C knockout inhibited the proliferation, migration, and invasion of SKOV3 cells; altered the gene expression patterns in these cells; and was closely associated with the PI3K/AKT pathway. Western blotting confirmed that CORO1C knockout reduced the levels of phosphorylated PI3K and AKT. Additionally, CORO1C knockout increased phosphatase and tensin homologs deleted on chromosome 10 (PTEN) protein expression, whereas CORO1C overexpression decreased it. In conclusion, this study demonstrated that high CORO1C levels in OC are associated with greater metastasis and worse prognosis. CORO1C negatively regulates PTEN expression, activates the PI3K/AKT pathway, and promotes OC cell malignancy In patients with OC, CORO1C may function as an effective therapeutic and predictive biomarker.

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CORO1C 通过 PI3K/AKT 信号通路调控卵巢癌细胞的恶性生物学行为并调节 mRNA 表达谱。
卵巢癌(OC)是一种多发的妇科肿瘤,近年来其全球发病率呈上升趋势。已知冠状病毒样肌动蛋白结合蛋白1C(CORO1C)可激活磷酸肌醇3-激酶(PI3K)-蛋白激酶B(AKT)通路并促进肿瘤进展。然而,它在 OC 中的作用仍不清楚。本研究探讨了CORO1C在OC恶性肿瘤中的作用。本研究采用实时定量聚合酶链反应(qRT-PCR)检测AKT和CORO1C mRNA在临床OC组织和细胞中的表达。免疫组化分析和免疫印迹法分别检测了 OC 组织和细胞中的蛋白表达。采用 3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)、划痕伤口愈合和 Transwell 试验检测细胞的增殖和迁移。利用 RNA-Seq 验证了 AKT 与 CORO1C 表达之间的关系。结果显示,CORO1C在临床OC组织和SKOV3细胞中高表达,与国际妇产科联盟(FIGO)的分期相关。此外,CORO1C敲除抑制了SKOV3细胞的增殖、迁移和侵袭,改变了这些细胞的基因表达模式,并与PI3K/AKT通路密切相关。Western 印迹证实,CORO1C 基因敲除降低了磷酸化 PI3K 和 AKT 的水平。此外,CORO1C 基因敲除增加了 10 号染色体上删除的磷酸酶和天丝同源物(PTEN)蛋白的表达,而 CORO1C 基因过表达则降低了其表达。总之,本研究表明,OC中CORO1C的高水平与更大的转移和更差的预后有关。CORO1C 负向调节 PTEN 的表达,激活 PI3K/AKT 通路,促进 OC 细胞恶性化 在 OC 患者中,CORO1C 可作为一种有效的治疗和预测生物标志物。
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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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