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CXC 趋化因子配体 16 和趋化因子(C-X-C 基序)受体 6 在胃癌中的表达作用及临床病理意义。

Role and clinicopathologic significance of CXC chemokine ligand 16 and chemokine (C-X-C motif) receptor 6 expression in gastric carcinomas.

机构信息

Department of Biochemistry and Molecular Biology, Institute of Pathology and Pathophysiology, College of Basic Medicine, China Medical University, Shenyang 110001, China.

出版信息

Hum Pathol. 2012 Dec;43(12):2299-307. doi: 10.1016/j.humpath.2011.08.027. Epub 2012 Aug 3.

Abstract

The chemokine ligand CXC chemokine ligand 16 and its receptor chemokine (C-X-C motif) receptor 6 are up-regulated in many types of cancer and give rise to more aggressive behavior by regulating proliferation and angiogenesis. To clarify the role and clinicopathologic significance of CXC chemokine ligand 16 and chemokine (C-X-C motif) receptor 6 expression in gastric carcinoma, their expression was examined by immunohistochemistry of tissue microarrays containing gastric carcinoma and nonneoplastic mucosa, reverse transcription-polymerase chain reaction, and Western blotting and by enzyme-linked immunosorbent assay to determine the CXC chemokine ligand 16 concentration in serum. Expression was compared with the clinicopathologic features of the carcinomas. All carcinoma and epithelial cells showed CXC chemokine ligand 16 and chemokine (C-X-C motif) receptor 6 messenger RNA expression to various degrees. Among 28 pairs of gastric carcinoma and normal tissues, there was higher CXC chemokine ligand 16 expression in carcinoma than in adjacent mucosa (P < .05), whereas the converse was true for chemokine (C-X-C motif) receptor 6 (P < .05). Nuclear CXC chemokine ligand 16 expression correlated inversely with the depth of invasion, lymphatic invasion, Union Internationale Contre le Cancer stage, and favorable prognosis. The serum CXC chemokine ligand 16 concentration was lower in male patients or patients 55 years or older than in female or younger patients, respectively (P < .05). Patients with lymphatic invasion or mixed-type carcinoma showed lower CXC chemokine ligand 16 concentrations than those with no lymphatic invasion or with diffuse-type carcinoma (P < .05). Aberrant expression of CXC chemokine ligand 16 and chemokine (C-X-C motif) receptor 6 might be involved in gastric carcinogenesis. The expression and serum concentration of CXC chemokine ligand 16 could indicate the aggressiveness and prognosis of gastric carcinomas.

摘要

趋化因子配体 CXC 趋化因子配体 16 及其受体趋化因子(C-X-C 基序)受体 6 在许多类型的癌症中上调,并通过调节增殖和血管生成导致更具侵袭性的行为。为了阐明趋化因子配体 CXC 16 和趋化因子(C-X-C 基序)受体 6 在胃癌中的表达的作用和临床病理意义,通过组织微阵列的免疫组织化学检查了它们的表达,该组织微阵列包含胃癌和非肿瘤性粘膜,逆转录-聚合酶链反应和 Western 印迹,并通过酶联免疫吸附试验测定血清中趋化因子配体 CXC 16 的浓度。将表达与癌的临床病理特征进行了比较。所有癌和上皮细胞均显示出不同程度的趋化因子配体 CXC 16 和趋化因子(C-X-C 基序)受体 6 信使 RNA 表达。在 28 对胃癌和正常组织中,癌组织中 CXC 趋化因子配体 16 的表达高于相邻粘膜(P <.05),而趋化因子(C-X-C 基序)受体 6 的表达则相反(P <.05)。核 CXC 趋化因子配体 16 的表达与浸润深度,淋巴浸润,国际抗癌联合会分期和良好的预后呈负相关。与女性或年龄较小的患者相比,男性或年龄较大的患者的血清 CXC 趋化因子配体 16 浓度较低(P <.05)。具有淋巴浸润或混合性癌的患者的 CXC 趋化因子配体 16 浓度低于无淋巴浸润或弥漫性癌的患者(P <.05)。CXC 趋化因子配体 16 和趋化因子(C-X-C 基序)受体 6 的异常表达可能参与胃癌的发生。CXC 趋化因子配体 16 的表达和血清浓度可以指示胃癌的侵袭性和预后。

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