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金属蛋白酶组织抑制剂(TIMPs)在肝细胞癌中的表达。

Expression of tissue inhibitors of metalloproteinases (TIMPs) in hepatocellular carcinoma.

作者信息

Joo Y E, Seo Y H, Lee W S, Kim H S, Choi S K, Rew J S, Park C S, Kim S J

机构信息

Department of Internal Medicine, Chonnam National University Medical School, Kwangju, Korea.

出版信息

Korean J Intern Med. 2000 Dec;15(3):171-8. doi: 10.3904/kjim.2000.15.3.171.

Abstract

BACKGROUND

Matrix metalloproteinases (MMPs) have been implicated in the remodelling of extracellular matrix (ECM), including basement membrane. ECM remodelling is associated with pathological processes, including hepatic fibrosis, tumor invasion and metastasis. Tissue inhibitors of metalloproteinase (TIMP)-1 and TIMP-2 were known to inhibit MMP-9 and MMP-2, respectively. In the present study, we examined the expression of TIMP-1 and TIMP-2 in surgical specimen pairs of hepatocellular carcinoma and nontumoral liver and the correlation between their expression and clinicopathological characteristics.

METHODS

The localization of both transcripts and protein of TIMP-1 and TIMP-2 was studied by using in situ hybridization and immunohistochemistry.

RESULTS

TIMP-1 and TIMP-2 mRNA transcripts were found in tumor cells, hepatocyte, sinusoidal cells, endothelial cells and stromal cells. Signal intensity of TIMP-1 was stronger than that of TIMP-2. The results of immunohistochemical stainings were concordant with those obtained by in situ hybridization. Expression of TIMP-1 and TIMP-2 was observed in tumorous tissue, in nontumorous tissue and in the portions of the tumors adjacent to the capsules. However, a clear difference in TIMP-1 and TIMP-2 mRNA expression was not observed among the three tissue types. The intensity of TIMP-2 expression was generally weaker than that of TIMP-1, and the intensity of TIMP-1 and TIMP-2 mRNA expression did not correlate with variable clinicopathological characteristics.

CONCLUSION

TIMPs was expressed in tumor cells and many cell types of the nontumoral liver. Further investigations for TIMPs' unknown functional role are needed.

摘要

背景

基质金属蛋白酶(MMPs)参与细胞外基质(ECM)重塑,包括基底膜重塑。ECM重塑与包括肝纤维化、肿瘤侵袭和转移在内的病理过程相关。金属蛋白酶组织抑制剂(TIMP)-1和TIMP-2分别已知可抑制MMP-9和MMP-2。在本研究中,我们检测了TIMP-1和TIMP-2在肝细胞癌手术标本与非肿瘤性肝组织配对样本中的表达情况,以及它们的表达与临床病理特征之间的相关性。

方法

采用原位杂交和免疫组化技术研究TIMP-1和TIMP-2转录本及蛋白的定位。

结果

在肿瘤细胞、肝细胞、窦状细胞、内皮细胞和基质细胞中发现了TIMP-1和TIMP-2 mRNA转录本。TIMP-1的信号强度强于TIMP-2。免疫组化染色结果与原位杂交结果一致。在肿瘤组织、非肿瘤组织以及肿瘤邻近包膜部分均观察到TIMP-1和TIMP-2的表达。然而,在这三种组织类型之间未观察到TIMP-1和TIMP-2 mRNA表达的明显差异。TIMP-2的表达强度总体上弱于TIMP-1,且TIMP-1和TIMP-2 mRNA表达强度与各种临床病理特征无关。

结论

TIMP在肿瘤细胞和非肿瘤性肝的多种细胞类型中表达。需要对TIMP未知的功能作用进行进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc1b/4531765/ec79dadb28e3/kjim-15-3-171-2f1.jpg

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