Characterization of tumor-derived mesenchymal stem cells potentially differentiating into cancer-associated fibroblasts in lung cancer

被引:35
作者
Arena, S. [1 ,2 ]
Salati, M. [3 ]
Sorgentoni, G. [4 ]
Barbisan, F. [5 ]
Orciani, M. [4 ]
机构
[1] Univ Torino, Dept Oncol, SP 142,Km 3-95, I-10060 Candiolo, TO, Italy
[2] IRCCS, Candiolo Canc Inst FPO, Candiolo, TO, Italy
[3] AOU Osped Riuniti, Unit Thorac Surg, Via Tronto 10-A, I-60126 Ancona, Italy
[4] Univ Politecn Marche, Dept Mol & Clin Sci Histol, Via Tronto 10-A, I-60020 Ancona, Italy
[5] AOU Osped Riuniti, Unit Pathol, Via Tronto 10-A, I-60126 Ancona, Italy
关键词
Lung cancer; Mesenchymal stem cells; Cancer-associated fibroblasts; IL6; CARCINOMA-ASSOCIATED FIBROBLASTS; STROMAL FIBROBLASTS; AMNIOTIC-FLUID; EGFR; RESISTANCE; MUTATIONS; GROWTH; MICROENVIRONMENT; INFLAMMATION; MSCS;
D O I
10.1007/s12094-018-1894-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
PurposeThe goal of this study was to understand if mesenchymal stem cells isolated from lung tumor tissue (T-MSCs) may differentiate into cancer associated fibroblasts (CAFs), that promote neoplastic progression, angiogenesis and metastasis in the epithelial solid tumors, mimicking the tumor microenvironmental influence.MethodsMSCs were been obtained from healthy (Control, C-MSCs) and tumor (T-MSCs) tissue of one patient who underwent a lobectomy for a lung adenocarcinoma pT1bN0. Isolated cells were characterized for the presence of molecular markers (identified by routine diagnostic characterization in differentiated tumoral cells), stemness properties, and CAF-related markers expression. Subsequently, cells were co-cultured with a lung adenocarcinoma cell line (A549 cells) to evaluate the effects on proliferation, oncogene expression and IL6 secretion.ResultsC- and T-MSCs did not present EGFR mutations unlike tumor tissue and showed a stem-like immunophenotype, characterized by the ability to differentiate towards osteo-, chondro- and adipogenic lineages. The expression of markers referred to CAFs (-SMA, HI-1, MMP11, VEGF, CXCL12, TGF-1, TGF-RII, IL6, TNF) was significantly higher in T-MSCs than in C-MSCs. The co-cultures with A549 cells led to the over-expression of selected oncogenes and to the increase of IL6 secretion in T-MSCs but not in C-MSCs.ConclusionsMSCs isolated from tumor tissue displayed distinct properties compared to MSCs isolated from healthy tissue, suggesting T-MSCs differentiation towards a CAF-related phenotype under the influence of the tumoral microenvironment.
引用
收藏
页码:1582 / 1591
页数:10
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