Prognostic value of the density of Wilms tumour protein 1 (WT-1) positive microvessels in stage IIA colorectal cancer

被引:0
作者
Barresi, Valeria [1 ]
Bonetti, Luca Reggiani [2 ]
Branca, Giovanni [1 ]
Vitarelli, Enrica [1 ]
Ieni, Antonio [1 ]
Tuccari, Giovanni [1 ]
机构
[1] AOU G Martino, Dept Human Pathol G Barresi, Via Consolare Valeria, I-98125 Messina, Italy
[2] Polyclin Modena, Dept Forens Med Lab & Pathol Anat, Via Pozzo, I-41124 Modena, Italy
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2016年 / 9卷 / 03期
关键词
Colorectal cancer; WT-1; microvessel density; prognosis; stage IIA; poorly differentiated clusters; POORLY DIFFERENTIATED CLUSTERS; AMERICAN JOINT COMMITTEE; COLON-CANCER; WT1; PROTEIN; SUPPRESSOR WT1; RISK-FACTORS; GENE-1; T-CELLS; EXPRESSION; CARCINOMA;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Stage IIA colorectal cancer (CRC) displays 5-year survival rate around 85%; hence it is not currently submitted to any adjuvant treatment. However a percentage of stage IIA CRCs undergoes disease progression and would benefit from additional therapies. In the aim to investigate whether Wilms Tumor-1 (WT-1) expression might represent a prognostic factor in stage IIA CRC, we analyzed its immunohistochemical expression in 90 stage IIA CRCs divided into two groups according to the evidence of disease progression. While WT-1 staining in the neoplastic cells was not significantly associated with any of the clinico-pathological parameters, the density of intra-tumoral microvessels positive for WT-1 (WT-1 MVD) was significantly higher in stage IIA CRCs characterized by disease progression compared to non-recurring tumours and it was significantly and independently associated with shorter disease-free survival. This study is the first to demonstrate that WT-1 MVD may be useful to discriminate high risk patients with stage IIA CRCs and who may benefit from adjuvant treatment. WT-1 expression in the tumor vessels, but not in the vessels of normal colorectal mucosa, suggests its possible role in tumor neo-angiogenesis and it may represent a target for novel anti-angiogenic therapies in stage IIA CRC at high risk of progression.
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收藏
页码:3115 / 3124
页数:10
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