乳腺癌
H&E染色
免疫组织化学
细胞外基质
医学
病理
病态的
基质
转移
染色
癌症
肿瘤科
内科学
化学
生物化学
作者
Rodrigo de Andrade Natal,José Vassallo,Geisilene Russano de Paiva Silva,Vitor B. Pelegati,Guilherme Oliveira Barbosa,Guilherme Rossi Assis de Mendonça,Caroline Bondarik,Sophie Derchain,Hernandes F. Carvalho,Carmen Sílvia Passos Lima,Carlos L. César,Luı́s Otávio Sarian
出处
期刊:Tumor Biology
[SAGE]
日期:2018-04-01
卷期号:40 (4): 101042831877095-101042831877095
被引量:51
标识
DOI:10.1177/1010428318770953
摘要
Second-harmonic generation microscopy represents an important tool to evaluate extracellular matrix collagen structure, which undergoes changes during cancer progression. Thus, it is potentially relevant to assess breast cancer development. We propose the use of second-harmonic generation images of tumor stroma selected on hematoxylin and eosin-stained slides to evaluate the prognostic value of collagen fibers analyses in peri and intratumoral areas in patients diagnosed with invasive ductal breast carcinoma. Quantitative analyses of collagen parameters were performed using ImageJ software. These parameters presented significantly higher values in peri than in intratumoral areas. Higher intratumoral collagen uniformity was associated with high pathological stages and with the presence of axillary lymph node metastasis. In patients with immunohistochemistry-based luminal subtype, higher intratumoral collagen uniformity and quantity were independently associated with poorer relapse-free and overall survival, respectively. A multivariate response recursive partitioning model determined 12.857 and 11.894 as the best cut-offs for intratumoral collagen quantity and uniformity, respectively. These values have shown high sensitivity and specificity to differentiate distinct outcomes. Values of intratumoral collagen quantity and uniformity exceeding the cut-offs were strongly associated with poorer relapse-free and overall survival. Our findings support a promising prognostic value of quantitative evaluation of intratumoral collagen by second-harmonic generation imaging mainly in the luminal subtype breast cancer.
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