4.5 Article

Potential anti-tumor effect of IFN-λ2 (IL-28A) against human lung cancer cells

期刊

LUNG CANCER
卷 78, 期 3, 页码 185-192

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.lungcan.2012.09.005

关键词

Type III interferon; IL-28A; Non-small cell lung cancer; EGFR mutation; Apoptosis; Bioluminescent imaging

资金

  1. Health and Labour Science Research Grants of the Ministry of Health. Labour, and Welfare (Research on Biological Resources)
  2. Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan [20591326, 23591627]
  3. Takeda Science Foundation
  4. Strategic Research Platform for Private Universities: matching fund subsidy from MEXT
  5. Grants-in-Aid for Scientific Research [23591627, 20591326] Funding Source: KAKEN

向作者/读者索取更多资源

Interferon (IFN)-lambda s (IL-28A/IL-28B/IL-29) classified as type III IFNs, are the latest members identified of the interferon family. As with type I IFNs such as IFN-alpha, type III IFNs share antiviral and antitumor activity and may have fewer side effects due to a more selective receptor distribution. Therefore, type III IFNs may be clinically useful for human viral and malignant diseases. Here we demonstrate the potential anti-tumor effect of IFN-lambda 2 (IL-28A) against human lung cancer cells. All lung cancer cell lines that we examined expressed both IFN-lambda receptors (IL-28R1 and IL-10R2). Lung cancer cells with epidermal growth factor receptor (EGFR) mutations were more sensitive to IFN-lambda 2 treatment compared with cells with KRAS mutations. HCC827 cells with an EGFR mutation treated with IFN-lambda 2 underwent growth suppression and apoptotic cell death by STAT1 phosphorylation. Administration of neutralizing antibodies to IFN-lambda inhibited caspase-3/7 activity induced by IFN-lambda 2. Finally, in vivo luminescent imaging also demonstrated the anti-tumor effect of IFN-lambda 2 in a cancer cell transplant animal model. Taken together, IFN-lambda 2 would be a new therapeutic agent for clinical lung cancers with EGFR mutations. (c) 2012 Elsevier Ireland Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据