Blockade of Leukotriene B4 Signaling Pathway Induces Apoptosis and Suppresses Cell Proliferation in Colon Cancer
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- Ihara Aya
- Department of Gastroenterology, Yokohama City University Graduate School of Medicine, Japan
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- Wada Koichiro
- Department of Pharmacology, Graduate School of Dentistry, Osaka University, Japan
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- Yoneda Masato
- Division of Gastroenterology, Yokohama City University School of Medicine, Japan
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- Fujisawa Nobutaka
- Division of Gastroenterology, Yokohama City University School of Medicine, Japan
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- Takahashi Hirokazu
- Division of Gastroenterology, Yokohama City University School of Medicine, Japan
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- Nakajima Atsushi
- Division of Gastroenterology, Yokohama City University School of Medicine, Japan
書誌事項
- 公開日
- 2007
- DOI
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- 10.1254/jphs.fp0060651
- 公開者
- 公益社団法人 日本薬理学会
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説明
We investigated whether leukotriene B4 (LTB4) and its signaling pathway play an important role in the progression of human colon cancer via a direct stimulation of cancer cell proliferation. Remarkable expression of LTB4 receptor 1 (BLT1) in human colon cancer tissues was detected by immunohistochemistry, and Western blot analysis revealed the BLT1 expression in cultured human colon cancer cell lines, Caco2 and HT29. The 5-lipoxygenase inhibitor AA-861 and LTB4-receptor antagonist U75302 showed negative effects on survival and proliferation of both Caco2 and HT-29 cells. The inhibition of cell proliferation is due to the apoptosis because nuclear condensation and increased annexin V expression were observed in the cells treated with AA-861 and U75302. Knockdown of BLT1 by small interfering RNA caused the suppression of BLT1 protein, resulting in the inhibition of cancer cell proliferation. Blockade of BLT1 by the receptor antagonist significantly suppresses the LTB4-stimulated extracellular signal-regulated kinase (ERK) activation in colon cancer cells. These results indicate that the blockade of the LTB4-signaling pathway induces apoptosis via the inhibition of ERK activation in colon cancer cells. The LTB4-signaling pathway might be a new therapeutic target for colon cancer.<br>
収録刊行物
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- Journal of Pharmacological Sciences
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Journal of Pharmacological Sciences 103 (1), 24-32, 2007
公益社団法人 日本薬理学会
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詳細情報 詳細情報について
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- CRID
- 1390282680153614208
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- NII論文ID
- 10024311869
- 130000074876
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- NII書誌ID
- AA11806667
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- ISSN
- 13478648
- 13478613
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- NDL書誌ID
- 8617850
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- PubMed
- 17220595
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- 本文言語コード
- en
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