Author
Listed:
- Kazuki Takada
- Tatsuro Okamoto
- Masaki Tominaga
- Koji Teraishi
- Takaki Akamine
- Shinkichi Takamori
- Masakazu Katsura
- Gouji Toyokawa
- Fumihiro Shoji
- Masaki Okamoto
- Yoshinao Oda
- Tomoaki Hoshino
- Yoshihiko Maehara
Abstract
Interleukin (IL)-38, a novel member of the IL-1 cytokine family, is homologous to IL-1 receptor antagonist (IL-1Ra) and IL-36Ra, and has been reported to act as an antagonist. IL-38 expression is found in tonsil, placenta, and spleen, and recent studies suggest an association between IL-38 and autoimmune diseases. However, whether IL-38 plays a role in carcinogenesis or cancer growth is unclear. In the present study, we identified increases in IL-38 expression by immunohistochemistry in multiple types of cancer cells. In the examination of 417 surgically resected primary lung adenocarcinomas, Fisher’s exact tests showed significant associations between high IL-38 expression and high tumor grades, an advanced T status, advanced N status, advanced stage, and the presence of pleural and vessel invasions. Survival analyses by the Kaplan-Meier method showed that patients with high expression of IL-38 had significantly shorter disease-free survival and shorter overall survival after surgery than patients with low expression of IL-38 (log-rank test: P = 0.0021 and P = 0.0035, respectively). Moreover, programmed cell death-ligand 1 (PD-L1)-positive cases showed higher expression of IL-38 than PD-L1-negative cases (Wilcoxon rank-sum test: P
Suggested Citation
Kazuki Takada & Tatsuro Okamoto & Masaki Tominaga & Koji Teraishi & Takaki Akamine & Shinkichi Takamori & Masakazu Katsura & Gouji Toyokawa & Fumihiro Shoji & Masaki Okamoto & Yoshinao Oda & Tomoaki H, 2017.
"Clinical implications of the novel cytokine IL-38 expressed in lung adenocarcinoma: Possible association with PD-L1 expression,"
PLOS ONE, Public Library of Science, vol. 12(7), pages 1-15, July.
Handle:
RePEc:plo:pone00:0181598
DOI: 10.1371/journal.pone.0181598
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