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胰腺癌中 CCL20/CCR6 的表达谱。

CCL20/CCR6 expression profile in pancreatic cancer.

机构信息

Dept. of General -, Visceral-, Vascular - and Paediatric Surgery, University of the Saarland, Homburg/Saar, Germany.

出版信息

J Transl Med. 2010 May 10;8:45. doi: 10.1186/1479-5876-8-45.

Abstract

BACKGROUND

CCL20 and its receptor CCR6 have been shown to play a role in the onset, development and metastatic spread of various gastrointestinal malignancies. In this study, the expression profile and clinical significance of the CCL20/CCR6 system in distinct benign, pre-malignant and malignant pancreatic tissues was investigated.

METHODS

Using RealTime-PCR, enzyme-linked immunosorbent assay (ELISA), Western Blot and immunohistochemistry, we have analyzed the expression profile of CCL20/CCR6 in resection specimens from patients with chronic pancreatitis (CP) (n = 22), pancreatic cystadenoma (PA) (n = 11) and pancreatic carcinoma (PCA) (n = 25) as well as in the respective matched normal pancreatic tissues.

RESULTS

CCL20 mRNA and protein was weakly expressed in normal pancreatic tissues and CP and PA specimens but significantly up-regulated in PCA (8-fold) as compared to the matched normal tissue (P < 0.05). Moreover, CCL20 mRNA and protein expression was significantly associated with advanced T-category in patients with PCA (P < 0.05). CCR6 mRNA showed a significant up-regulation in all three disease entities as compared to normal tissues (P < 0.05, respectively).

CONCLUSION

CCL20 and CCR6 were significantly up-regulated in PCA as compared to the normal pancreatic tissue and CCL20 was significantly associated with advanced T-category in PCA patients. This suggests that CCL20 and CCR6 play a role in the development and progression of PCA and may constitute potential targets for novel treatment strategies.

摘要

背景

CCL20 和其受体 CCR6 已被证实参与多种胃肠道恶性肿瘤的发生、发展和转移扩散。在本研究中,我们研究了 CCL20/CCR6 系统在不同良性、癌前和恶性胰腺组织中的表达谱及其临床意义。

方法

通过实时 PCR、酶联免疫吸附试验(ELISA)、Western Blot 和免疫组织化学,我们分析了慢性胰腺炎(CP)(n=22)、胰腺囊腺瘤(PA)(n=11)和胰腺腺癌(PCA)(n=25)患者的手术标本以及相应的匹配正常胰腺组织中 CCL20/CCR6 的表达谱。

结果

CCL20 mRNA 和蛋白在正常胰腺组织和 CP 和 PA 标本中弱表达,但在 PCA 中显著上调(与匹配的正常组织相比上调 8 倍,P<0.05)。此外,CCL20 mRNA 和蛋白表达与 PCA 患者的晚期 T 分期显著相关(P<0.05)。与正常组织相比,CCR6 mRNA 在所有三种疾病实体中均显著上调(分别为 P<0.05)。

结论

与正常胰腺组织相比,CCL20 和 CCR6 在 PCA 中显著上调,并且 CCL20 在 PCA 患者中与晚期 T 分期显著相关。这表明 CCL20 和 CCR6 在 PCA 的发生和发展中起作用,并且可能构成新的治疗策略的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4808/2877001/8300bdd18c80/1479-5876-8-45-1.jpg

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