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白细胞介素-8网络在大肠腺瘤-癌序列中的动态变化。

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

作者信息

Cui Guanglin, Yuan Aping, Goll Rasmus, Vonen Barthold, Florholmen Jon

机构信息

Laboratory of Gastroenterology, Faculty of Medicine, Institute of Clinical Medicine, University of Tromsø, 9037 Tromsø, Norway.

出版信息

Cancer Immunol Immunother. 2009 Nov;58(11):1897-905. doi: 10.1007/s00262-009-0702-y. Epub 2009 Apr 7.

Abstract

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.

摘要

白细胞介素-8(IL-8)网络参与结直肠癌(CRC)的进展。然而,迄今为止其在腺瘤-癌转变过程中的作用尚未得到充分研究。为了评估IL-8网络在结直肠腺瘤-癌序列中的动态变化,我们通过定量实时PCR(Q-PCR)检测了53例结直肠腺瘤、44例CRC和18例对照的结直肠活检组织中IL-8 mRNA水平,并通过免疫组织化学(IHC)和双重免疫组织化学检测了肿瘤微环境中IL-8及其受体(IL-8RA和IL-8RB)的表达。结果显示,与对照组相比,癌前病变(腺瘤)中的组织IL-8 mRNA水平开始升高,在CRC中更高。值得注意 的是,IL-8 mRNA水平的升高与腺瘤中发育异常等级的增加相关,也与CRC中杜克分期的增加平行。免疫组织化学结果显示,IL-8及其受体IL-8RA和IL-8RB在基质以及腺瘤/癌细胞中均有观察到。通过双重免疫组织化学,IL-8表达在肿瘤基质中的巨噬细胞、淋巴细胞和成肌纤维细胞中得以表征。进一步的双重免疫组织化学鉴定出IL-8受体(IL-8RA和IL-8RB)与CD34阳性肿瘤相关微血管在腺瘤和CRC中均有共表达。因此,我们得出结论,肿瘤微环境中激活的IL-8网络可能作为腺瘤进展和腺瘤-癌转变的重要调节因子发挥作用。

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