NUSAP1通过激活Hedgehog信号通路调控基底细胞癌的迁移、侵袭和DNA损伤。

IF 2.2 4区 医学 Q3 PHYSIOLOGY Physiology international Pub Date : 2023-06-12 DOI:10.1556/2060.2023.00227
Yanjun Zhu, Yan Liu, Liwen Zhang, Shihua Zeng, Wen Xu
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引用次数: 0

摘要

背景:基底细胞癌(Basal cell carcinoma, BCC)是一种发病率越来越高的常见皮肤癌。核仁和纺锤体相关蛋白1 (NUSAP1)是一种参与多种癌症发展的细胞增殖相关蛋白。然而,其在BCC中的作用和机制尚不清楚。方法:采用western blot法检测NUSAP1的表达。通过将NUSAP1和si NUSAP1过表达质粒转染到TE354中进行功能增益和功能损失测定。T细胞。通过细胞计数试剂盒-8 (CCK-8)、菌落形成、transwell、流式细胞术和western blot等方法探讨NUSAP1在BCC中的作用和作用机制。结果:NUSAP1在TE354中高表达。T细胞。过表达NUSAP1可提高TE354细胞活力、集落形成数量、迁移和侵袭细胞数量以及RAD51的相对蛋白表达,降低TE354细胞的凋亡率和γ - h2ax的相对蛋白表达。T细胞。经TE354处理后,上述指标均呈相反结果。T细胞被NUSAP1下调。此外,将NUSAP1过表达质粒转染到TE354中,可以增加Hedgehog信号通路相关蛋白的相对表达量。但转染si NUSAP1到TE354后,其表达减少。T细胞。结论:NUSAP1在BCC中促进增殖、迁移和侵袭,减弱细胞凋亡和DNA损伤,参与了Hedgehog信号通路的激活。
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NUSAP1 regulates basal cell carcinoma migration, invasion and DNA damage through activation of the Hedgehog signaling pathway.

Background: Basal cell carcinoma (BCC) is a prevalent cutaneous cancer with an increasing incidence. Nucleolar and spindle associated protein 1 (NUSAP1) is a cell proliferation-related protein that participates in the development of various cancers. However, its role and mechanism in BCC remain elusive.

Methods: The expression of NUSAP1 was detected by western blot. Gain- and loss-of-function assays were performed through the transfection of overexpression plasmid of NUSAP1 and si NUSAP1 into TE354.T cells. The role and mechanism of action of NUSAP1 in BCC were explored by cell counting kit-8 (CCK-8), colony formation, transwell, flow cytometry and western blot assays.

Results: NUSAP1 was highly expressed in TE354.T cells. Overexpression of NUSAP1 enhanced cell viability, colony forming numbers, numbers of migrated and invasive cells and the relative protein expression of RAD51, but reduced the apoptosis rate and the relative protein expression of γH2AX in TE354.T cells. Inverse results were obtained in these indicators after TE354.T cells were downregulated with NUSAP1. Moreover, the relative expression of proteins involved in the Hedgehog signaling pathway was increased by transfection of the overexpression plasmid of NUSAP1 into TE354.T cells, but decreased by the transfection of si NUSAP1 into TE354.T cells.

Conclusion: Both gain- and loss-of-function results revealed that NUSAP1 promoted proliferation, migration and invasion but attenuated apoptosis and DNA damage in BCC, which was involved in the activation of the Hedgehog signaling pathway.

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来源期刊
Physiology international
Physiology international Medicine-Physiology (medical)
CiteScore
3.40
自引率
0.00%
发文量
37
期刊介绍: The journal provides a forum for important new research papers written by eminent scientists on experimental medical sciences. Papers reporting on both original work and review articles in the fields of basic and clinical physiology, pathophysiology (from the subcellular organization level up to the oranizmic one), as well as related disciplines, including history of physiological sciences, are accepted.
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