Dynamic changes of interleukin-8 network along the colorectal adenoma–carcinoma sequence

被引:3
|
作者
Guanglin Cui
Aping Yuan
Rasmus Goll
Barthold Vonen
Jon Florholmen
机构
[1] University of Tromsø,Laboratory of Gastroenterology, Faculty of Medicine, Institute of Clinical Medicine
[2] University Hospital of North Norway,Department of Gastroenterology
[3] University Hospital of North Norway,Department of Gastrointestinal Surgery
来源
Cancer Immunology, Immunotherapy | 2009年 / 58卷
关键词
Chemokine; Carcinogenesis; Adenoma–carcinoma sequence;
D O I
暂无
中图分类号
学科分类号
摘要
The interleukin-8 (IL-8) network is involved in the colorectal cancer (CRC) progression. However, its role during the adenoma–carcinoma transition to date has not been fully investigated. To evaluate the dynamic changes of IL-8 network along the colorectal adenoma–carcinoma sequence, we examined the tissue IL-8 mRNA level in colorectal biopsies from 53 colorectal adenomas, 44 CRCs and 18 controls by quantitative real-time PCR (Q-PCR), and the expressions of IL-8 and its receptors (IL-8RA and IL-8RB) in the tumor microenvironment by immunohistochemistry (IHC) and double IHCs. The results showed that the tissue IL-8 mRNA level began to increase in the precancerous lesions (adenomas) as compared with the controls and became even higher in the CRCs. Significantly, the increase of IL-8 mRNA levels was associated with the increase of dysplastic grades in the adenomas, and also paralleled to the increase of Duke’s stages in the CRCs. IHC results revealed that IL-8 and its receptors, IL-8RA and IL-8RB, were observed both in the stroma and in the adenomatous/cancerous cells. By double IHCs, the IL-8 expression was characterized in macrophages, lymphocytes and myofibroblasts in the tumor stroma. Further double IHC identified the co-expression of IL-8 receptors (IL-8RA and IL-8RB) with CD34 positive tumor-associated microvessels in both the adenomas and CRCs. We, therefore, conclude that activated IL-8 network in the tumor microenvironment may function as a significant regulatory factor for the adenoma progression and the adenoma–carcinoma transition.
引用
收藏
页码:1897 / 1905
页数:8
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