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LASP1基因对人结直肠癌LOVO细胞增殖、迁移和凋亡的影响及其机制

徐益平, 尚韬

徐益平, 尚韬. LASP1基因对人结直肠癌LOVO细胞增殖、迁移和凋亡的影响及其机制[J]. 肿瘤防治研究, 2023, 50(10): 955-959. DOI: 10.3971/j.issn.1000-8578.2023.23.0301
引用本文: 徐益平, 尚韬. LASP1基因对人结直肠癌LOVO细胞增殖、迁移和凋亡的影响及其机制[J]. 肿瘤防治研究, 2023, 50(10): 955-959. DOI: 10.3971/j.issn.1000-8578.2023.23.0301
XU Yiping, SHANG Tao. Effects and Mechanism of LASP1 on Proliferation, Migration, and Apoptosis of Human Colorectal Cancer LOVO Cells[J]. Cancer Research on Prevention and Treatment, 2023, 50(10): 955-959. DOI: 10.3971/j.issn.1000-8578.2023.23.0301
Citation: XU Yiping, SHANG Tao. Effects and Mechanism of LASP1 on Proliferation, Migration, and Apoptosis of Human Colorectal Cancer LOVO Cells[J]. Cancer Research on Prevention and Treatment, 2023, 50(10): 955-959. DOI: 10.3971/j.issn.1000-8578.2023.23.0301

LASP1基因对人结直肠癌LOVO细胞增殖、迁移和凋亡的影响及其机制

基金项目: 

浙江省医药卫生科技计划项目 2021KY823

详细信息
    作者简介:

    徐益平(1986-),女,本科,技师,主要从事肿瘤病理技术研究,ORCID: 0009-0002-2018-1219

    通信作者:

    尚韬(1988-),男,硕士,主治医师,主要从事肛肠疾病研究,E-mail: shangtaosci@163.com,ORCID: 0009-0009-8321-3776

  • 中图分类号: R735.3

Effects and Mechanism of LASP1 on Proliferation, Migration, and Apoptosis of Human Colorectal Cancer LOVO Cells

Funding: 

Zhejiang Province Medical and Health Technology Plan Project 2021KY823

More Information
  • 摘要:
    目的 

    探讨LASP1基因表达对人结肠癌(LOVO)细胞增殖、迁移以及侵袭能力的影响及其作用机制。

    方法 

    分别构建LASP1过表达质粒和LASP1干扰质粒转染LOVO细胞,qRT-PCR验证LASP1 mRNA转染结果。MTT法、Tunel染色分别检测细胞增殖活性和细胞的凋亡情况,细胞划痕和Transwell实验检测细胞迁移和侵袭能力。Western blot测定细胞LASP1、p-FAK/FAK、p-AKT/AKT蛋白表达。

    结果 

    质粒转染成功。LASP1过表达的LOVO细胞的增殖、迁移和侵袭能力增加,细胞凋亡率降低,细胞中LASP1、p-FAK/FAK、p-AKT/AKT蛋白表达升高(P < 0.01)。而敲减LOVO细胞中LASP1的表达后,细胞增殖、迁移和侵袭能力减弱,细胞凋亡率增加,细胞中LASP1、p-FAK/FAK、p-AKT/AKT蛋白表达降低(P < 0.01)。

    结论 

    LASP1可正向调控FAK/AKT信号通路,促进LOVO细胞的增殖、迁移以及侵袭能力。

     

    Abstract:
    Objective 

    To explore the effects and mechanism of LASP1 gene expression on the proliferation, migration, and invasion of human colorectal cancer (LOVO) cells.

    Methods 

    LASP1 overexpression plasmids and LASP1 interference plasmids were constructed and transfected to LOVO cells. qRT-PCR was used to detect LASP1 mRNA expression and validate the transfection. MTT method and Tunel staining were used to detect cell proliferation and apoptosis, respectively, and scratch test and Transwell test were employed to determine the migration and invasion abilities of cells. Western blot was applied to analyze the expression of LASP1, p-FAK/FAK, and p-AKT/AKT protein in cells.

    Results 

    The plasmids were successfully transfected. LASP1 overexpression increased the proliferation, migration, and invasion of LOVO cells, decreased the apoptosis, and increased LASP1, p-FAK/FAK, p-AKT/AKT protein expression (P < 0.01). LASP1 knockdown reduced the proliferation, migration, and invasion of LOVO cells, increased the apoptosis, and decreased LASP1, p-FAK/FAK, and p-AKT/AKT protein expression (P < 0.01).

    Conclusion 

    LASP1 positively regulates the FAK/AKT signaling pathway to promote the proliferation, migration, and invasion of LOVO cells.

     

  • Competing interests: The authors declare that they have no competing interests.
    利益冲突声明:
    所有作者均声明不存在利益冲突。
    作者贡献:
    徐益平:数据分析及文章撰写与修改
    尚韬:实验思路构思及指导
  • 图  1   LASP1过表达或沉默对LOVO细胞迁移及侵袭能力的影响

    Figure  1   Effects of LASP1 overexpression or silence on migration and invasion of LOVO cells

    图  2   LASP1过表达或沉默对LOVO细胞凋亡的影响(Tunel染色)

    Figure  2   Effects of LASP1 overexpression or silence on apoptosis of LOVO Cells (Tunel staining)

    图  3   LASP1过表达或沉默对LOVO细胞相关蛋白表达的影响

    Figure  3   Effects of LASP1 overexpression or silence on related protein expression in LOVO cells

    表  1   引物序列

    Table  1   Primer sequence

    下载: 导出CSV

    表  2   qRT-PCR检测LOVO细胞转染后LASP1的表达

    Table  2   LASP1 mRNA expression in transfected LOVO cells detected by qRT-PCR

    下载: 导出CSV

    表  3   LASP1过表达或沉默对LOVO细胞存活的影响

    Table  3   Effects of overexpression or silencing of LASP1 on the survival of LOVO cells

    下载: 导出CSV
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出版历程
  • 收稿日期:  2023-03-21
  • 修回日期:  2023-06-04
  • 网络出版日期:  2024-01-12
  • 刊出日期:  2023-10-24

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