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MIB-1与核仁组成区嗜银蛋白(AgNORs)双重染色在原发性乳腺癌中的临床意义

Clinical significance of double staining of MIB-1 and AgNORs in primary breast carcinoma.

作者信息

Kidogawa Hideo, Nanashima Atsushi, Yano Hiroshi, Matsumoto Megumi, Yasutake Toru, Nagayasu Takeshi

机构信息

Division of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.

出版信息

Anticancer Res. 2005 Nov-Dec;25(6B):3957-62.

PMID:16309183
Abstract

BACKGROUND

Argyrophilic nucleolar organizer regions (AgNORs) and MIB-1 as proliferating activities have been applied separately to assess the malignant potential of cancer cells. We conducted staining of AgNORs and MIB-1 in 42 surgically-resected invasive breast carcinomas.

MATERIALS AND METHODS

Paraffin-embedded sections were used for double staining and the mean AgNOR counts in 100 MIB-1-positive and -negative cells were calculated.

RESULTS

The mean AgNOR count in MIB-1-positive cells was significantly higher than in MIB-1-negative ones. AgNOR counts in MIB-1-positive tumors were significantly higher in tumors > or =2 cm and those with positive nodes. Multivariate analysis identified the AgNOR count in MIB-1-positive tumors as the only independent factor related to node metastasis. Survival of patients with lower counts of AgNORs in MIB-1-positive tumors was significantly better compared to those with higher counts.

CONCLUSION

Double staining of MIB-1 and AgNORs is useful for predicting lymph node metastasis and prognosis of patients with breast carcinoma.

摘要

背景

嗜银核仁组织区(AgNORs)和MIB-1作为增殖活性指标已分别用于评估癌细胞的恶性潜能。我们对42例手术切除的浸润性乳腺癌进行了AgNORs和MIB-1染色。

材料与方法

采用石蜡包埋切片进行双重染色,并计算100个MIB-1阳性和阴性细胞中的平均AgNOR计数。

结果

MIB-1阳性细胞中的平均AgNOR计数显著高于MIB-1阴性细胞。在肿瘤直径≥2 cm和有阳性淋巴结的MIB-1阳性肿瘤中,AgNOR计数显著更高。多因素分析确定MIB-1阳性肿瘤中的AgNOR计数是与淋巴结转移相关的唯一独立因素。MIB-1阳性肿瘤中AgNOR计数较低的患者生存率明显高于计数较高的患者。

结论

MIB-1和AgNORs双重染色有助于预测乳腺癌患者的淋巴结转移和预后。

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2
Histopathological study comparing upstream binding factor expression and AgNOR staining.比较上游结合因子表达和 AgNOR 染色的组织病理学研究。
Cell Prolif. 2012 Aug;45(4):345-51. doi: 10.1111/j.1365-2184.2012.00829.x.