CXCL2型
CXCL1型
趋化因子受体
CXCL5型
癌症研究
白细胞介素8
趋化因子
免疫组织化学
病理
医学
肿瘤科
生物
内科学
受体
趋化因子受体
细胞因子
作者
Yurie Yamamoto,Kenji Kuroda,Tomohiro Sera,Atsushi Sugimoto,Shuhei Kushiyama,Sadaaki Nishimura,Shingo Togano,Tomohisa Okuno,Mami Yoshii,Tatsuro Tamura,Takahiro Toyokawa,Hiroaki Tanaka,Kazuya Muguruma,Masaichi Ohira,Masakazu Yashiro
出处
期刊:Anticancer Research
[International Institute of Anticancer Research (IIAR) Conferences 1997. Athens, Greece. Abstracts]
日期:2019-12-01
卷期号:39 (12): 6645-6652
被引量:44
标识
DOI:10.21873/anticanres.13879
摘要
We have previously reported that chemokine (C-X-C motif) receptor 2 (CXCR2) signaling was associated with the malignant progression of gastric cancer (GC). We thus examined the clinicopathological significance of CXCR2 ligands, CXCL1, CXCL2, CXCL3, CXCL5, CXCL6, CXCL7, and CXCL8, in GC.The expression of CXCR2 ligands in 590 GC cases was investigated by immunohistochemistry.The expression was as follows: CXCL1, 46.2% (257/557); CXCL2, 20.7% (122/590); CXCL3, 17.1% (101/589); CXCL5/CXCL6, 2.9% (17/589); CXCL7, 36.4% (215/590); and CXCL8 1.7% (10/585) of the cases. High invasion depth was correlated with CXCL1 expression. Lymph node metastasis and peritoneal cytology positivity were correlated with high expression of CXCL1 and CXCL7. The prognoses of the CXCL1-positive patients were significantly poorer than those of the CXCL1-negative patients (p<0.001).Among the CXCR2 ligands, CXCL7 and especially CXCL1, might play an important role in the malignant progression of GC via CXCR2 signaling.
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