首页> 外文期刊>Journal of Clinical Pathology >Stromal nitric oxide synthase (NOS) expression correlates with the grade of mammary phyllodes tumour.
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Stromal nitric oxide synthase (NOS) expression correlates with the grade of mammary phyllodes tumour.

机译:间质一氧化氮合酶(NOS)的表达与乳腺叶状肿瘤的等级有关。

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BACKGROUND: Nitric oxide synthase (NOS), particularly endothelial and inducible forms (e/i-NOS), are expressed in various cancers, including breast cancer. In mammary fibroepithelial lesions, NOS expression in stromal cells has been reported to be lower in fibroadenomas than in phyllodes tumours. AIMS: To investigate NOS expression in phyllodes tumours of varying degrees of malignancy. METHODS: One hundred and sixty seven mammary phyllodes tumours (97 benign, 47 borderline malignant, and 23 frankly malignant) were evaluated for e-NOS and i-NOS expression by immunohistochemistry. Correlations with previously reported expression of stromal vascular growth factor (VEGF) and microvessel density were also performed. RESULTS: Stromal expression of e-NOS was absent, weak, moderate, and strong in 43%, 31%, 13%, and 13% of benign tumours; 17%, 26%, 13%, and 44% of borderline malignant tumours; and 17%, 35%, 13%, and 35% of frankly malignant tumours, respectively. Stromal expression of i-NOS was 77%, 18%, 4%, and 1% in benign tumours; 42%, 28%, 19%, and 11% in borderline malignant tumours; and 43%, 13%, 26%, and 18% in frankly malignant tumours, respectively. Stromal expression of both i-NOS and e-NOS was significantly different between the benign and malignant (borderline and frank) groups of phyllodes tumours (p<0.0001). Furthermore, the expression of i-NOS correlated with stromal VEGF expression and microvessel density. The expression of NOS in the epithelial cells was strong, and showed no differences between the different groups of tumours. CONCLUSIONS: Higher stromal expression of NOS in phyllodes tumours is associated with malignancy, suggesting a possible role in malignant progression, particularly metastasising potential.
机译:背景:一氧化氮合酶(NOS),尤其是内皮和可诱导形式(e / i-NOS)在包括乳腺癌在内的各种癌症中都有表达。在乳腺纤维上皮病变中,据报道,在纤维腺瘤中基质细胞中的NOS表达比叶状肿瘤低。目的:研究NOS在不同恶性程度的叶状肿瘤中的表达。方法:采用免疫组织化学方法评估了167个乳腺叶状肿瘤(97例良性,47例交界性恶性肿瘤和23例坦率恶性肿瘤)的e-NOS和i-NOS表达。还进行了与先前报道的基质血管生长因子(VEGF)表达和微血管密度的相关性。结果:e-NOS的基质表达在良性肿瘤中不存在,弱,中和强,分别占43%,31%,13%和13%。边缘性恶性肿瘤的17%,26%,13%和44%;分别占坦率的恶性肿瘤的17%,35%,13%和35%。 i-NOS的基质表达在良性肿瘤中分别为77%,18%,4%和1%。边缘性恶性肿瘤分别占42%,28%,19%和11%;坦率的恶性肿瘤分别为43%,13%,26%和18%。 i-NOS和e-NOS的基质表达在叶状肿瘤的良性和恶性(边界线和坦率)组之间显着不同(p <0.0001)。此外,i-NOS的表达与基质VEGF表达和微血管密度相关。 NOS在上皮细胞中的表达很强,并且在不同肿瘤组之间没有差异。结论:叶状肿瘤中NOS的较高基质表达与恶性肿瘤有关,提示其可能在恶性进展中发挥重要作用,尤其是转移潜力。

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