Basic & Clinical Medicine ›› 2022, Vol. 42 ›› Issue (10): 1549-1554.doi: 10.16352/j.issn.1001-6325.2022.10.1549

• Original Articles • Previous Articles     Next Articles

rL-RVG inhibits the proliferation and migration of human small cell lung cancer cell line NCI-H446

LIANG Bing1, YAN Yu-lan2*   

  1. 1. Department of Respiratory Medicine, Kunshan Hospital of Traditional Chinese Medicine, Kunshan 215300;
    2. Department of Respiratory Medicine, the Affiliated People's Hospital of Jiangsu University, Zhenjiang 212000, China
  • Received:2021-05-28 Revised:2022-01-07 Online:2022-10-05 Published:2022-09-23
  • Contact: * ylyan2005@163.com

Abstract: Objective To investigate the effect and potential mechanism of recombinant Newcastle disease virus rL-RVG on proliferation and migration of human small cell lung cancer cell line NCI-H446. Methods NCI-H446 cells were divided into 3 groups: incubated with PBS, Newcastle disease virus(NDV) and rL-RVG, respectively. Immunofluorescence assay was used to detect the expression of RVG and NDV protein. MTT assay was used to determine the anti-proliferation of the virus. The cell migration was detected by scratch test and Transwell method. Immuno-fluorescence assay was used to detect the expression of E-cadherin and MMP2 proteins. Results After infection, rL-RVG stably expressed in NCI-H446 cell with high infection efficiency.The scratch distance in rL-RVG group was significantly shorter than that in NDV group and control group(P<0.05). In the Transwell experiment, the number of cells crossing the compartment in the rL-RVG group were significantly less than that in the control group(P<0.05). MMP2 protein expression was down-regulated in rL-RVG group, while E-cadherin protein expression was up-regulated(P<0.05), compared with NDV group and control group. Conclusions rL-RVG could inhibit the proliferation of NCI-H446 cell with the potential mechanism of effects on cell migration through regulating E-cadherin and MMP2.

Key words: small cell lung cancer, Newcastle disease virus, migration

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