Differential expression of neural markers in KIT and PDGFRA wild-type gastrointestinal stromal tumours

被引:20
|
作者
Pantaleo, Maria A. [1 ,2 ]
Astolfi, Annalisa [2 ]
Nannini, Margherita [1 ]
Ceccarelli, Claudio [3 ]
Formica, Serena [2 ]
Santini, Donatella [3 ]
Heinrich, Michael C. [4 ,5 ]
Corless, Christopher [4 ,5 ]
Dei Tos, Angelo Paolo [6 ]
Paterini, Paola [2 ]
Catena, Fausto [7 ]
Maleddu, Alessandra [1 ]
Saponara, Maristella [1 ]
Di Battista, Monica [1 ]
Biasco, Guido [1 ,2 ]
机构
[1] Univ Bologna, S Orsola Malpighi Hosp, Dept Hematol & Oncol Sci LA Seragnoli, I-40138 Bologna, Italy
[2] Univ Bologna, Interdept Ctr Canc Res G Prodi, I-40138 Bologna, Italy
[3] Univ Bologna, S Orsola Malpighi Hosp, Dept Radiol & Histopathol Sci, Surg Pathol Unit, I-40138 Bologna, Italy
[4] Portland VA Med Ctr, Dept Med, Portland, OR USA
[5] Oregon Hlth & Sci Univ, Knight Canc Inst, Portland, OR 97201 USA
[6] Gen Hosp Treviso, Dept Oncol, Treviso, Italy
[7] Univ Bologna, S Orsola Malpighi Hosp, Emergency Surg & Transplant Dept, I-40138 Bologna, Italy
关键词
gene expression profiling; GIST; ICC; ICC mature; ICC precursor; IGF1R; KIT; PDGFRA; INTERSTITIAL-CELLS; C-KIT; MUTATIONS; CAJAL; GISTS; COMMON; RECEPTOR; STOMACH;
D O I
10.1111/j.1365-2559.2011.04071.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: To compare the genomic signatures of wildtype (WT) and mutated GISTs and the murine interstitial cells of Cajal (ICCs) to find markers of cell differentiation and other functions that may identify cells that give rise to WT tumours. Methods and results: We analysed the gene expression profiles of a total of 30 tumour samples (four WT GISTs and 26 mutated GISTs), selected the genes most differentially expressed (P < 0.001: 448 probe sets) and validated these results by quantitative polymerase chain reaction (PCR) and immunohistochemistry. In addition, we conducted a meta-analysis merging data from human GISTs with a genomic data set from murine ICCs. The gene expression profiles of WT and mutated GISTs differed profoundly, especially in the expression of those genes restricted primarily to neural tissues. We found that mature ICCs are more similar to mutated GISTs than WT GISTs. Conclusions: WT GISTs have different genomic profiles from both mutated GISTs and murine mature ICCs. Considering that IGF1R expression is common to both WT GISTs and putative precursor ICCs, this study suggests that WT GISTs may derive either from ICCs at a different step of differentiation or from a different cell of origin.
引用
收藏
页码:1071 / 1080
页数:10
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