de Oliveira Barros Eliane Gouvêa, Palumbo Antonio, Mello Pedro Lucas Prado, de Mattos Rômulo Medina, da Silva Julianna Henriques, Pontes Bruno, Viana Nathan Bessa, do Amaral Rackele Ferreira, Lima Flavia Regina Souza, da Costa Nathalia Meireles, Palmero Celia Yelimar, Miranda-Alves Leandro, Takiya Christina Maeda, Nasciutti Luiz Eurico
Programa de Pesquisa em Biologia Celular e do Desenvolvimento, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
LPO/COPEA, Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Clin Exp Metastasis. 2014 Apr;31(4):461-74. doi: 10.1007/s10585-014-9640-y. Epub 2014 Feb 1.
Tumor establishment, growth, and survival are supported by interactions with microenvironment components. Here, we investigated whether the interactions between prostate cancer cells and cortical astrocytes are associated to a potential role for astrocytes in tumor establishment. We demonstrate that astrocytes interact in vitro with prostatic cancers cells derived from different metastatic sites. Astrocytes and their secreted extracellular matrix, stimulate DU145 cell (a brain-derived prostate tumor cell line) proliferation while inhibiting cell death and modulating the expression of several genes related to prostate cancer progression, suggesting the activation of EMT process in these cells. In contrast, DU145 cells and their conditioned medium inhibited cell proliferation and induced cell death of astrocytes. On the other hand, the astrocytes were unable to significantly induce an increment of LNCaP cell (a lymph node-derived prostate tumor cell line) proliferative activity. In addition, LNCaP cells were also unable to induce cell death of astrocytes. Thus, we believe that DU145 cells, but not LNCaP cells, present an even more aggressive behavior when interacting with astrocytes. These results provide an important contribution to the elucidation of the cellular mechanisms involved in the brain microenvironment colonization.
肿瘤的形成、生长和存活受到与微环境成分相互作用的支持。在此,我们研究了前列腺癌细胞与皮质星形胶质细胞之间的相互作用是否与星形胶质细胞在肿瘤形成中的潜在作用相关。我们证明星形胶质细胞在体外与源自不同转移部位的前列腺癌细胞相互作用。星形胶质细胞及其分泌的细胞外基质刺激DU145细胞(一种脑源性前列腺肿瘤细胞系)增殖,同时抑制细胞死亡并调节与前列腺癌进展相关的几个基因的表达,提示这些细胞中EMT过程的激活。相反,DU145细胞及其条件培养基抑制星形胶质细胞的增殖并诱导其细胞死亡。另一方面,星形胶质细胞不能显著诱导LNCaP细胞(一种淋巴结源性前列腺肿瘤细胞系)增殖活性的增加。此外,LNCaP细胞也不能诱导星形胶质细胞的细胞死亡。因此,我们认为DU145细胞而非LNCaP细胞在与星形胶质细胞相互作用时表现出更具侵袭性的行为。这些结果为阐明参与脑微环境定植的细胞机制做出了重要贡献。