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Fibrotic focus and hypoxia in male breast cancer

机译:男性乳腺癌的纤维化病灶和缺氧

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Fibrotic focus is a scar-like lesion near the center of a carcinoma and has been associated with high-grade, lymph node metastases and poor survival in female breast cancers. Hypoxia is suggested to be the crucial link between fibrotic focus and aggressive tumor phenotype and is also itself a poor prognostic marker. We here set out to study fibrotic focus and hypoxia in male breast cancer for the first time. In a group of 134 male breast cancer patients, the presence and size of a fibrotic focus and the expression of three hypoxia-related immunohistochemical stainings, hypoxia-inducible factor-1α, carbonic anhydrase IX and Glut-1 were studied in correlation with clinicopathological features and prognosis. Fibrotic focus was seen in 25% of the male breast cancer cases and was correlated with hypoxia-inducible factor-1α overexpression (P=0.023), high grade (P=0.005), high mitotic activity (P=0.005) and lymph node metastases (P=0.037). Hypoxia-inducible factor-1α-positive tumors were more often high grade (P=0.003) and HER2 amplified (P=0.005). Glut-1 expression was also more common in grade 3 tumors (P=0.038), but no association between carbonic anhydrase IX and any clinicopathological feature was found. Fibrotic focus >8?mm and hypoxia-inducible factor-1α overexpression were correlated with decreased patients’ outcome (P=0.035 and 0.008, respectively). Hypoxia-inducible factor-1α overexpression was an independent and the most powerful predictor of survival in multivariate analysis (P=0.029; hazard ratio 2.5). In conclusion, the presence of a fibrotic focus is associated with hypoxia-inducible factor-1α overexpression, and both are associated with aggressive tumor phenotype and poor survival in male breast cancer. These markers seem to have similar clinical importance as previously reported in female breast cancer.
机译:纤维化病灶是癌中心附近的疤痕样病变,与女性乳腺癌的高级别淋巴结转移和不良的生存有关。低氧被认为是纤维化病灶与侵袭性肿瘤表型之间的关键联系,本身也是不良的预后标志物。我们在这里着手研究男性乳腺癌的纤维化病灶和低氧。在一组134名男性乳腺癌患者中,研究了纤维化病灶的大小和存在以及与低氧相关的免疫组织化学染色,低氧诱导因子-1α,碳酸酐酶IX和Glut-1的三种表达与临床病理特征的关系。和预后。在25%的男性乳腺癌患者中发现了纤维化病灶,并且与低氧诱导因子-1α过表达(P = 0.023),高等级(P = 0.005),高有丝分裂活性(P = 0.005)和淋巴结相关转移(P = 0.037)。缺氧诱导因子-1α阳性肿瘤多为高级别(P = 0.003)和HER2扩增(P = 0.005)。 Glut-1的表达在3级肿瘤中也更为常见(P = 0.038),但未发现碳酸酐酶IX与任何临床病理特征之间存在关联。纤维化病灶> 8?mm和缺氧诱导因子-1α过表达与患者预后降低相关(分别为P = 0.035和0.008)。缺氧诱导因子-1α的过量表达是多变量分析中生存的独立且最有力的预测因子(P = 0.029;危险比2.5)。总之,纤维化病灶的存在与缺氧诱导因子-1α的过表达有关,两者均与雄性乳腺癌的侵袭性肿瘤表型和不良的存活率有关。这些标志物似乎具有与先前在女性乳腺癌中报道的相似的临床重要性。

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