Department of Clinical and Molecular Medicine, University of Rome La Sapienza S Andrea Hospital, Rome, Italy.
PLoS One. 2011;6(7):e21320. doi: 10.1371/journal.pone.0021320. Epub 2011 Jul 18.
Malignant pleural effusions (MPEs) could represent an excellent source to culture a wide variety of cancer cells from different donors. In this study, we set up culture conditions for cancer cells deriving from MPEs of several patients affected by the most frequent form of lung cancer, namely the subset of non small cell lung cancers (NSCLC) classified as Lung Adenocarcinomas (AdenoCa) which account for approximately 40% of lung cancer cases. AdenoCa malignant pleural effusions gave rise to in vitro cultures both in adherent and/or in spheroid conditions in almost all cases analyzed. We characterized in greater detail two samples which showed the most efficient propagation in vitro. In these samples we also compared gene profiles of spheroid vs adherent cultures and identified a set of differentially expressed genes. Finally we achieved efficient tumor engraftment in recipient NOD/SCID mice, also upon inoculation of small number of cells, thus suggesting indirectly the presence of tumor initiating cells.
恶性胸腔积液(MPEs)可以作为培养来自不同供体的各种癌细胞的绝佳来源。在这项研究中,我们为源自多位患有最常见肺癌形式(即非小细胞肺癌(NSCLC)亚组)的 MPE 患者的癌细胞建立了培养条件。肺癌腺癌(AdenoCa)约占肺癌病例的 40%。AdenoCa 恶性胸腔积液几乎在所有分析的病例中都在贴壁和/或球体条件下产生了体外培养物。我们详细研究了两个显示体外增殖效率最高的样本。在这些样本中,我们还比较了球体与贴壁培养物的基因谱,并鉴定了一组差异表达基因。最后,我们通过向受体 NOD/SCID 小鼠接种少量细胞,也实现了有效的肿瘤移植,这间接提示存在肿瘤起始细胞。