論文

査読有り 国際誌
2021年11月1日

The novel long noncoding RNA AU021063, induced by IL-6/Arid5a signaling, exacerbates breast cancer invasion and metastasis by stabilizing Trib3 and activating the Mek/Erk pathway.

Cancer letters
  • Kishan Kumar Nyati
  • ,
  • Shigeru Hashimoto
  • ,
  • Shailendra Kumar Singh
  • ,
  • Murat Tekguc
  • ,
  • Hozaifa Metwally
  • ,
  • Yu-Chen Liu
  • ,
  • Daisuke Okuzaki
  • ,
  • Yohannes Gemechu
  • ,
  • Sujin Kang
  • ,
  • Tadamitsu Kishimoto

520
開始ページ
295
終了ページ
306
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.canlet.2021.08.004
出版者・発行元
Elsevier BV

Interleukin (IL-6) is a pleotropic cytokine with both tumor-promoting and -inhibitory effects on breast cancer growth. However, the mechanisms governing the outcome of IL-6 on cancer progression remain to be clarified. Our study unraveled a novel long noncoding RNA (lncRNA) AU021063 downstream of IL-6 signaling. We found that IL-6 induced the expression of AU021063 predominantly in breast cancer compared to other cancer types. Mechanistically, IL-6 induced AT-rich interactive domain 5a (Arid5a) expression, which promotes the transcription of AU021063. In turn, AU021063 promotes breast cancer metastasis through stabilizing tribbles homolog 3 (Trib3) and activating Mek/Erk signaling pathway. Genetic ablation of either Arid5a, AU021063 or Trib3 abolished breast cancer metastasis in vitro and in vivo. Overall, our study highlights the importance of IL-6-Arid5a-AU021063 axis in regulating breast cancer invasiveness and metastasis, which may provide potential novel therapeutics for breast cancer.

リンク情報
DOI
https://doi.org/10.1016/j.canlet.2021.08.004
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/34389433
ID情報
  • DOI : 10.1016/j.canlet.2021.08.004
  • ISSN : 0304-3835
  • PubMed ID : 34389433

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