Nicola Maria-Helena A, Bizon Rosana, Machado Janaina J S, Sollero Tereza, Rodarte Renato S, Nobre João S, Magalhães Maurício M, Takiya Christina M, Borojevic Radovan
Departamento de Histologia e Embriologia, Instituto de Ciências Biomédicas, and Programa Avançado de Biologia Celular Aplicada a Medicina, Hospital Universitário Clementino Fraga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Clin Exp Metastasis. 2003;20(5):471-9. doi: 10.1023/a:1025462417256.
The apparently dormant breast cancer micrometastases in haemopoietic marrow are correlated with distant metastatic carcinoma dissemination. We studied in vitro interactions of carcinoma cells with adjacent stromata, using connective tissue cell cultures from breast and bone marrow samples of normal donors, comparing them to the pericancerous breast tissue and bone marrows of 12 selected patients with invasive breast carcinomas. Cancer cells were detected by immunocytochemistry and RT-PCR in all the bone marrows and in most blood samples of the studied patients. We monitored the growth and interaction of carcinoma MCF-7 cells with the stromata. The normal breast stroma sustained typical massive cancer growth. The pericancerous breast stroma induced the invasive mesenchymal pattern of growth. Normal bone marrow stroma induced the same conversion and was highly adhesive, retaining the cells in the stroma, but carcinoma patients' bone marrow stromata underwent low adhesive interactions with cancer cells, releasing them potentially into the circulation. The semi-quantitative RT-PCR indicated an enhanced expression of the hepatocyte growth factor and its receptor c-met in breast and bone marrow stromata of cancer patients. The input of cancer cells into the normal bone marrow may induce modifications of the local microenvironment, favourable for growth and release of carcinoma cells into the systemic circulation, which correlate with the poor prognosis of patients with bone marrow micrometastases.
造血骨髓中看似处于休眠状态的乳腺癌微转移与远处转移性癌扩散相关。我们利用正常供体乳腺和骨髓样本的结缔组织细胞培养,研究癌细胞与相邻基质的体外相互作用,并将其与12例选定的浸润性乳腺癌患者的癌旁乳腺组织和骨髓进行比较。通过免疫细胞化学和逆转录聚合酶链反应(RT-PCR)在所有研究患者的骨髓和大多数血液样本中检测到癌细胞。我们监测了MCF-7癌细胞与基质的生长和相互作用。正常乳腺基质支持典型的大量癌细胞生长。癌旁乳腺基质诱导侵袭性间充质生长模式。正常骨髓基质诱导相同的转化且具有高度粘附性,将细胞保留在基质中,但癌症患者的骨髓基质与癌细胞发生低粘附性相互作用,可能将它们释放到循环中。半定量RT-PCR表明,癌症患者乳腺和骨髓基质中肝细胞生长因子及其受体c-met的表达增强。癌细胞进入正常骨髓可能会诱导局部微环境的改变,有利于癌细胞生长并释放到体循环中,这与骨髓微转移患者的不良预后相关。