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High co-expression of IL-34 and M-CSF correlates with tumor progression and poor survival in lung cancers

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/68545

Title: High co-expression of IL-34 and M-CSF correlates with tumor progression and poor survival in lung cancers
Authors: Baghdadi, Muhammad Browse this author
Endo, Hiraku Browse this author
Takano, Atsushi Browse this author →KAKEN DB
Ishikawa, Kozo Browse this author
Kameda, Yosuke Browse this author
Wada, Haruka Browse this author →KAKEN DB
Miyagi, Yohei Browse this author →KAKEN DB
Yokose, Tomoyuki Browse this author
Ito, Hiroyuki Browse this author
Nakayama, Haruhiko Browse this author
Daigo, Yataro Browse this author →KAKEN DB
Suzuki, Nao Browse this author →KAKEN DB
Seino, Ken-ichiro Browse this author →KAKEN DB
Issue Date: 11-Jan-2018
Publisher: Nature Publishing Group
Journal Title: Scientific reports
Volume: 8
Start Page: 418
Publisher DOI: 10.1038/s41598-017-18796-8
Abstract: Despite recent advances in diagnosis and treatment of lung cancers, the 5-year survival rate remains unsatisfactory, which necessitates the identification of novel factors that associates with disease progression and malignant degree for improving diagnostic and therapeutic strategies. Recent progress in cancer immunology research has unveiled critical roles for colony stimulating factor 1 receptor (CSF1R) in multiple aspects of the tumor microenvironment. CSF1R is expressed on tumor-associated macrophages (TAMS), and mediates important pro-tumorigenic functions. CSF1R also provides critical autocrine signals that promote cancer cell survival and proliferation. Activation of CSF1R can be achieved by two independent ligands; macrophage colony-stimulating factor (M-CSF) and interleukin 34 (IL-34). Accordingly, the expression of these ligands in cancer is expected to result in poor prognosis. In this study, we show that IL-34 and M-CSF expression correlates with poor survival in a cohort of lung cancer patients. Importantly, high co-expression of IL-34 and M-CSF associates with the poorest survival compared to cancers that show weak or absent expression of the two ligands. Furthermore, high expression of IL-34 and M-CSF associates with advanced stages of lung cancers. Together, these results indicate a correlation between IL-34/M-CSF expression with poor survival and disease progression in lung cancer patients.
Rights: http://creativecommons.org/licenses/by/4.0/
Type: article
URI: http://hdl.handle.net/2115/68545
Appears in Collections:遺伝子病制御研究所 (Institute for Genetic Medicine) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 清野 研一郎

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