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人类结直肠癌细胞中肿瘤相关微血管中非肥大细胞组胺的表达。

The expression of non-mast histamine in tumor associated microvessels in human colorectal cancers.

机构信息

Department of Medicine, the Second Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.

出版信息

Pathol Oncol Res. 2013 Apr;19(2):311-6. doi: 10.1007/s12253-012-9584-y. Epub 2012 Dec 14.

Abstract

Angiogenesis is essential for the growth, expansion and metastasis of human colorectal cancers (CRCs). Histamine produced by mast cells is a potent proangiogenic factor. However, the significance of non-mast cell expressing histamine in the tumor microenvironment remains unknown. In this study, we evaluated the histamine positive microvessels with the specific marker for biosynthesis of histamine L-histidine decarboxylase (HDC) in the CRC tumor microenvironment. The relationship between HDC positive microvessel density (HDC-MVD) and clinical pathological parameters was assessed. The results revealed that HDC-MVD in the tumor microenvironment of CRCs was significantly increased as compared with the controls. CRC patients with lymph node invasion had a particularly higher density of HDC-MVD than those without. The density of HDC-MVD accounted for ~79 % of CD34 positive MVD in CRCs and double IHC analysis demonstrated that these HDC positive microvessels were mostly CD34 positive microvessels and with a high proliferative activity. Our results suggest that histamine expressed in microvessels could be an additional cellular source and involved in the cancer invasion through promoting angiogenesis in human CRCs.

摘要

血管生成对于人类结直肠癌(CRC)的生长、扩张和转移至关重要。肥大细胞产生的组胺是一种有效的促血管生成因子。然而,肿瘤微环境中非肥大细胞表达的组胺的意义尚不清楚。在这项研究中,我们评估了 CRC 肿瘤微环境中具有组胺生物合成特异性标记物 L-组氨酸脱羧酶(HDC)的阳性微血管。评估了 HDC 阳性微血管密度(HDC-MVD)与临床病理参数之间的关系。结果表明,CRC 肿瘤微环境中的 HDC-MVD 明显高于对照组。与无淋巴结侵犯的 CRC 患者相比,有淋巴结侵犯的 CRC 患者的 HDC-MVD 密度更高。HDC-MVD 的密度约占 CRC 中 CD34 阳性 MVD 的 79%,双重免疫组化分析表明,这些 HDC 阳性微血管主要是 CD34 阳性微血管,且具有较高的增殖活性。我们的结果表明,血管中表达的组胺可能是另一个细胞来源,并通过促进人 CRC 中的血管生成而参与癌症侵袭。

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