| Literature DB >> 34389433 |
Kishan Kumar Nyati1, Shigeru Hashimoto2, Shailendra Kumar Singh3, Murat Tekguc4, Hozaifa Metwally2, Yu-Chen Liu5, Daisuke Okuzaki6, Yohannes Gemechu2, Sujin Kang2, Tadamitsu Kishimoto7.
Abstract
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.Entities:
Keywords: Arid5a; Breast cancer; Interleukin-6; LncRNA; Metastasis
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Year: 2021 PMID: 34389433 DOI: 10.1016/j.canlet.2021.08.004
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679