Mannello Ferdinando, Fabbri Laura, Ciandrini Eleonora, Tonti Gaetana A
Institute of Histology and Laboratory Analysis, Faculty of Sciences and Technologies, University Carlo Bo, Urbino, Italy.
Cell Oncol. 2008;30(1):51-61. doi: 10.1155/2008/812193.
Erythropoietin (Epo) is an important regulator of erythropoiesis, and controls proliferation and differentiation of both erythroid and non-erythroid tissues. Epo is actively synthesized by breast cells during lactation, and also plays a role in breast tissues promoting hypoxia-induced cancer initiation. Our aims are to perform an exploratory investigation on the Epo accumulation in breast secretions from healthy and cancer patients and its localization in breast cancer cells.
Epo was determined by ELISA, immunoprecipitation, western blot and immunocytochemical analyses in 130 Nipple Aspirate Fluids (NAF) from 102 NoCancer and 28 Breast Cancer (BC) patients, comparing results with those found in 10 milk, 45 serum samples and breast cancer cell lines.
Epo levels in NAFs were significantly higher than those in milk and serum. No difference in Epo electrophoretic mobility was found among NAF, milk and serum samples, and conditioned cell culture medium. Immunolocalization of intracellular Epo in ductal cells floating in BC NAFs was similar to those of cancer cell lines. No significant correlation between TNM classification and Epo in NAFs from BC patients was found. Significantly higher Epo concentration was found in NAF from BC patients compared to NoCancer.
We demonstrate that breast epithelial cells are a source of Epo in breast microenvironment, suggesting the presence of a paracrine/autocrine Epo function in NAFs, triggering off intracellular signaling cascade with subsequent BC initiation.
促红细胞生成素(Epo)是红细胞生成的重要调节因子,可控制红系和非红系组织的增殖与分化。Epo在哺乳期由乳腺细胞主动合成,在乳腺组织中对缺氧诱导的癌症起始也起作用。我们的目的是对健康和癌症患者乳腺分泌物中的Epo积累及其在乳腺癌细胞中的定位进行探索性研究。
采用酶联免疫吸附测定(ELISA)、免疫沉淀、蛋白质印迹法和免疫细胞化学分析,对102名非癌症患者和28名乳腺癌患者的130份乳头抽吸液(NAF)中的Epo进行检测,并将结果与10份乳汁、45份血清样本及乳腺癌细胞系中的结果进行比较。
NAF中的Epo水平显著高于乳汁和血清中的水平。在NAF、乳汁、血清样本及条件细胞培养基之间,未发现Epo电泳迁移率存在差异。漂浮在乳腺癌NAF中的导管细胞内Epo的免疫定位与癌细胞系中的相似。在乳腺癌患者的NAF中,未发现TNM分类与Epo之间存在显著相关性。与非癌症患者相比,乳腺癌患者NAF中的Epo浓度显著更高。
我们证明乳腺上皮细胞是乳腺微环境中Epo的来源,提示NAF中存在旁分泌/自分泌Epo功能,可触发细胞内信号级联反应,随后引发乳腺癌。