4.3 Article

Suppression of radiation-induced migration of non-small cell lung cancer through inhibition of Nrf2-Notch Axis

Journal

ONCOTARGET
Volume 8, Issue 22, Pages 36603-36613

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.16622

Keywords

Nrf2; ionizing radiation; Notch1; EMT; NSCLC

Funding

  1. Key program of National Natural Science Foundation of China [U1432248, U1632270]
  2. Ministry of science and technology national key R D project [2016YFC0904600]
  3. National Natural Science Foundation of China [11665003]
  4. Scientific Technology Research Projects of Gansu Province [0702NKDA045, 0801NKDA001, 092NKDA034]

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Nuclear factor E2 related factor 2 (Nrf2) is a transcription factor that is associated with tumor growth and resistance to radiation. The canonical Notch signaling pathway is also crucial for maintaining non-small cell lung cancer (NSCLC). Aberrant Nrf2 and Notch signaling has repeatedly been showed to facilitate metastasis of NSCLC. Here, we show that radiation induce Nrf2 and Notch1 expression in NSCLC. Knockdown of Nrf2 enhanced radiosensitivity of NSCLC and reduced epithelial-tomesenchymal transition. Importantly, we found that knockdown of Nrf2 dramatically decreased radiation-induced NSCLC invasion and significantly increased E-cadherin, but reduced N-cadherin and matrix metalloproteinase (MMP)-2/9 expression. We found that Notch1 knockdown also upregulated E-cadherin and suppressed N-cadherin expression. Nrf2 contributes to NSCLC cell metastatic properties and this inhibition correlated with reduced Notch1 expression. These results establish that Nrf2 and Notch1 downregulation synergistically inhibit radiation-induced migratory and invasive properties of NSCLC cells.

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