Heparanase expression and localization in different types of human lung cancer

被引:13
作者
Fernandes dos Santos, Teresa Cristina [1 ]
Gomes, Angelica Maciel [2 ]
Machado Paschoal, Marcos Eduardo [3 ]
Stelling, Mariana Paranhos [2 ]
Barral Dodd Rumjanek, Vivian Mary [4 ]
do Rosario Junior, Alyson [5 ]
Valiante, Paulo Marcos [6 ]
Madi, Kalil [6 ]
Pereira de Souza, Heitor Siffert [5 ]
Goncalves Pavao, Mauro Sergio [2 ]
Lima Castelo-Branco, Morgana Teixeira [1 ]
机构
[1] Univ Fed Rio de Janeiro, ICB, Lab Imunol Celular, Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Lab Bioquim & Biol Celular Glicoconjugados, Inst Bioquim Med Leopoldo Meis, Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, Inst Doencas Torax, Hosp Univ Clementino Fraga Filho, Rio De Janeiro, Brazil
[4] Univ Fed Rio de Janeiro, Lab Imunol Tumoral, Inst Bioquim Med Leopoldo Meis, Rio De Janeiro, Brazil
[5] Univ Fed Rio de Janeiro, Lab Multidisciplinar Pesquisa, Hosp Univ Clementino Fraga Filho, Rio De Janeiro, Brazil
[6] Univ Fed Rio de Janeiro, Serv Anat Patol, Hosp Univ Clementino Fraga Filho, Rio De Janeiro, Brazil
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2014年 / 1840卷 / 08期
关键词
Heparanase; Adenocarcinoma; Squamous cell carcinoma; Large cell carcinoma; Small cell carcinoma; SMALL-CELL CARCINOMA; TUMOR PROGRESSION; SULFATE; GLYCOSAMINOGLYCANS; ANGIOGENESIS;
D O I
10.1016/j.bbagen.2014.04.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Heparanase is the only known mammalian glycosidase capable of cleaving heparan sulfate chains. The expression of this enzyme has been associated with tumor development because of its ability to degrade extracellular matrix and promote cell invasion. Methods: We analyzed heparanase expression in lung cancer samples to understand lung tumor progression and malignancy. Of the samples from 37 patients, there were 14 adenocarcinomas, 13 squamous cell carcinomas, 5 large cell carcinomas, and 5 small cell carcinomas. Immunohistochemistry was performed to ascertain the expression and localization of heparanase. Results: All of the tumor types expressed heparanase, which was predominantly localized within the cytoplasm and nucleus. Significant enzyme expression was also observed in cells within the tumor microenvironment, such as fibroblasts, epithelial cells, and inflammatory cells. Adenocarcinomas exhibited the strongest heparanase staining intensity and the most widespread heparanase distribution. Squamous cell carcinomas, large cell carcinomas, and small cell carcinomas had a similar subcellular distribution of heparanase to adenocarcinomas but the distribution was less widespread. Heparanase expression tended to correlate with tumor node metastasis (TNM) staging in non-small cell lung carcinoma. Conclusion: In this study, we showed that heparanase was localized to the cytoplasm and nucleus of tumor cells and to cells within the microenvironment in different types of lung cancer. This enzyme exhibited a differential distribution based on the type of lung tumor. General significance: Elucidating the heparanase expression patterns in different types of lung cancer increased our understanding of the crucial role of heparanase in lung cancer biology. This article is part of a Special Issue entitled Matrix-mediated cell behaviour and properties. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:2599 / 2608
页数:10
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