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Article

Activation of NLRP3 inflammasome enhances the proliferation and migration of A549 lung cancer cells

  • Authors:
    • Yanli Wang
    • Hui Kong
    • Xiaoning Zeng
    • Wenrui Liu
    • Zailiang Wang
    • Xiaopei Yan
    • Hong Wang
    • Weiping Xie
  • View Affiliations / Copyright

    Affiliations: Department of Respiratory Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, P.R. China
  • Pages: 2053-2064
    |
    Published online on: January 18, 2016
       https://doi.org/10.3892/or.2016.4569
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Abstract

Lung cancer is the leading cause of cancer death, and it is widely accepted that chronic inflammation is an important risk for the development of lung cancer. Now, it is recognized that the nucleotide-binding and oligomerization domain (NOD) like receptors (NLRs)-containing inflammasomes are involved in cancer-related inflammation. This study was designed to investigate the effects of NLR family pyrin domain containing protein 3 (NLRP3) inflammasome on the proliferation and migration of lung adenocarcinoma cell line A549. Using 5-ethynyl-2'-deoxyuridine (EdU) incorporation assay, scratch assay, and Transwell migration assay, we showed that activation of the NLRP3 inflammasome by LPS+ATP enhanced the proliferation and migration of A549 cells. Western blot analysis showed that activation of phosphorylation of Akt, ERK1/2, CREB and the expression of Snail increased, while the expression of E-cadherin decreased after the activation of NLRP3 inflammasome. Moreover, these effects were inhibited by the following treatments: i) downregulating the expression of NLRP3 by short hairpin RNA (shRNA) interference, ii) inhibiting the activation of NLRP3 inflammasome with a caspase-1 inhibitor, iii) blocking the interleukin-1β (IL-1β) and IL-18 signal transduction with IL-1 receptor antagonist (IL-1Ra) and IL-18 binding protein (IL-18BP). Collectively, these results indicate that NLRP3 inflammasome plays a vital role in regulating the proliferation and migration of A549 cells and it might be a potential target for the treatment of lung cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Wang Y, Kong H, Zeng X, Liu W, Wang Z, Yan X, Wang H and Xie W: Activation of NLRP3 inflammasome enhances the proliferation and migration of A549 lung cancer cells. Oncol Rep 35: 2053-2064, 2016.
APA
Wang, Y., Kong, H., Zeng, X., Liu, W., Wang, Z., Yan, X. ... Xie, W. (2016). Activation of NLRP3 inflammasome enhances the proliferation and migration of A549 lung cancer cells. Oncology Reports, 35, 2053-2064. https://doi.org/10.3892/or.2016.4569
MLA
Wang, Y., Kong, H., Zeng, X., Liu, W., Wang, Z., Yan, X., Wang, H., Xie, W."Activation of NLRP3 inflammasome enhances the proliferation and migration of A549 lung cancer cells". Oncology Reports 35.4 (2016): 2053-2064.
Chicago
Wang, Y., Kong, H., Zeng, X., Liu, W., Wang, Z., Yan, X., Wang, H., Xie, W."Activation of NLRP3 inflammasome enhances the proliferation and migration of A549 lung cancer cells". Oncology Reports 35, no. 4 (2016): 2053-2064. https://doi.org/10.3892/or.2016.4569
Copy and paste a formatted citation
x
Spandidos Publications style
Wang Y, Kong H, Zeng X, Liu W, Wang Z, Yan X, Wang H and Xie W: Activation of NLRP3 inflammasome enhances the proliferation and migration of A549 lung cancer cells. Oncol Rep 35: 2053-2064, 2016.
APA
Wang, Y., Kong, H., Zeng, X., Liu, W., Wang, Z., Yan, X. ... Xie, W. (2016). Activation of NLRP3 inflammasome enhances the proliferation and migration of A549 lung cancer cells. Oncology Reports, 35, 2053-2064. https://doi.org/10.3892/or.2016.4569
MLA
Wang, Y., Kong, H., Zeng, X., Liu, W., Wang, Z., Yan, X., Wang, H., Xie, W."Activation of NLRP3 inflammasome enhances the proliferation and migration of A549 lung cancer cells". Oncology Reports 35.4 (2016): 2053-2064.
Chicago
Wang, Y., Kong, H., Zeng, X., Liu, W., Wang, Z., Yan, X., Wang, H., Xie, W."Activation of NLRP3 inflammasome enhances the proliferation and migration of A549 lung cancer cells". Oncology Reports 35, no. 4 (2016): 2053-2064. https://doi.org/10.3892/or.2016.4569
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