Carduner Ludovic, Agniel Rémy, Kellouche Sabrina, Picot Cédric R, Blanc-Fournier Cécile, Leroy-Dudal Johanne, Carreiras Franck
Institut des Matériaux, Université de Cergy-Pontoise, Cergy-Pontoise Cedex, France.
Biochim Biophys Acta. 2013 Oct;1830(10):4885-97. doi: 10.1016/j.bbagen.2013.06.023. Epub 2013 Jun 26.
Intra-abdominal ascites is a complication of ovarian cancers and constitutes a permissive microenvironment for metastasis. Since fibronectin and vitronectin are key actors in ovarian cancer progression, we investigated their occurrence and molecular characteristics in various ascites fluids and the influence of these ascites-derived proteins on cell behavior.
Fibronectin and vitronectin were investigated by immunoblotting within various ascites fluids. A combined affinity-based protocol was developed to purify both proteins from the same sample. Each purified protein was characterized with regard to its molecular features (molecular mass of isoforms, tryptophan intramolecular environment, hydrodynamic radii), and its influence on cell adhesion.
Fibronectin and vitronectin were found in all tested ascites. Several milligrams of purified proteins were obtained from ascites of varying initial volumes. Molecular mass isoforms and conformational lability of proteins differed according to the ascites of origin. When incorporated into the cancer cell environment, ascites-derived fibronectin and vitronectin supported cell adhesion and migration with various degrees of efficiency, and induced the recruitment of integrins into focal contacts.
To our knowledge, this is the first combined purification of two extracellular matrix proteins from a single pathological sample containing a great variety of bioactive molecules. This study highlights that ascites-derived fibronectin and vitronectin exhibit different properties depending on the ascites.
Investigating the relationships between the molecular properties of ascites components and ovarian cancer cell phenotype according to the ascites may be critical for a better understanding of the recurrence of this lethal disease and for further biomarker identification.
腹腔腹水是卵巢癌的一种并发症,是转移的有利微环境。由于纤连蛋白和玻连蛋白是卵巢癌进展中的关键因子,我们研究了它们在各种腹水中的存在情况和分子特征,以及这些腹水来源的蛋白质对细胞行为的影响。
通过免疫印迹法研究各种腹水中的纤连蛋白和玻连蛋白。开发了一种基于亲和的联合方案,从同一样品中纯化这两种蛋白质。对每种纯化的蛋白质的分子特征(同工型分子量、色氨酸分子内环境、流体动力学半径)及其对细胞黏附的影响进行了表征。
在所有测试的腹水中均发现了纤连蛋白和玻连蛋白。从不同初始体积的腹水中获得了几毫克纯化的蛋白质。蛋白质的分子量同工型和构象稳定性因腹水来源而异。当整合到癌细胞环境中时,腹水来源的纤连蛋白和玻连蛋白以不同程度的效率支持细胞黏附和迁移,并诱导整合素募集到粘着斑中。
据我们所知,这是首次从含有多种生物活性分子的单一病理样本中联合纯化两种细胞外基质蛋白。这项研究强调,腹水来源的纤连蛋白和玻连蛋白根据腹水表现出不同的特性。
根据腹水研究腹水成分的分子特性与卵巢癌细胞表型之间的关系,对于更好地理解这种致命疾病的复发以及进一步鉴定生物标志物可能至关重要。