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

被引:33
作者
Cui, Guanglin [1 ,2 ]
Yuan, Aping [1 ,2 ]
Goll, Rasmus [1 ,2 ]
Vonen, Barthold [3 ]
Florholmen, Jon [1 ,2 ]
机构
[1] Univ Tromso, Inst Clin Med, Lab Gastroenterol, Fac Med, N-9037 Tromso, Norway
[2] Univ Hosp N Norway, Dept Gastroenterol, N-9038 Tromso, Norway
[3] Univ Hosp N Norway, Dept Gastrointestinal Surg, N-9038 Tromso, Norway
关键词
Chemokine; Carcinogenesis; Adenoma-carcinoma sequence; CELLS IN-VITRO; ANGIOGENIC SWITCH; COLON-CARCINOMA; MESSENGER-RNA; GROWTH-FACTOR; INFLAMMATORY CYTOKINES; CANCER-CELLS; EXPRESSION; IL-8; PROGRESSION;
D O I
10.1007/s00262-009-0702-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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:1899 / 1907
页数:9
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