首页> 外文期刊>Modern Pathology >PDGF-A, PDGF-R|[beta]|, TGF|[beta]|3 and bone morphogenic protein-4 in desmoplastic small round cell tumors with EWS-WT1 gene fusion product and their role in stromal desmoplasia: an immunohistochemical study
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PDGF-A, PDGF-R|[beta]|, TGF|[beta]|3 and bone morphogenic protein-4 in desmoplastic small round cell tumors with EWS-WT1 gene fusion product and their role in stromal desmoplasia: an immunohistochemical study

机译:具有EWS-WT1基因融合产物的增生性小圆形细胞肿瘤中PDGF-A,PDGF-R |β|,TGF |β| 3和骨形态发生蛋白4及其在间质性增生中的作用:免疫组织化学研究

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Histologically, desmoplastic small round cell tumor is composed of the characteristic neoplastic small round cells with divergent differentiation, and distinct desmoplastic stroma. Genetically, the tumor shows a characteristic 11;22 translocation, involving the EWS gene on chromosome 22 and the WT1gene on chromosome 11 to produce an EWS-WT1 fusion gene which generates a chimeric protein functioning as a novel transcription factor that activates expression of target genes such as PDGF-A. Expression of PDGF-A, a potent growth factor for fibroblasts, has been detected in desmoplastic small round cell tumors and has been linked to the characteristic desmoplasia in these tumors. Bone morphogenic proteins, which are members of the TGF superfamily play a complex role in regulating cell growth and differentiation and bone formation but have not been evaluated in desmoplastic small round cell tumors. In all, 24 desmoplastic small round cell tumors with EWS-WT1 fusion product confirmed by RT-PCR analysis were evaluated for expression of PDGF-A, PDGF-R, TGF3 and bone morphogenic protein-4 by standard immunohistochemical methods with antigen retrieval on paraffin sections. Immunoreactivity was evaluated semiquantitively. Tumor-associated desmoplasia was quantified using a three-tier scale on hematoxylin- and eosin-stained sections. Desmoplastic small round cell tumors showed variable immunoreactivity with TGF3 (21/24), BMP4 (14/21), PDGF-A (19/24) and PDGF-R (16/22). Less frequently, the stromal cells showed reactivity with TGF3, PDGF-R and PDGF-A. Tumor-associated desmoplasia was prominent in eight, intermediate in seven and weak in nine cases. There was no correlation between tumor-associated desmoplasia and the markers tested except PDGF-A. In contrast to a previous study, our study showed that the level of PDGF-A expression inversely correlated with tumor-associated desmoplasia. Other targets of the EWS-WT1 transcription factor other than PDGF-A may be directly responsible for the prominent tumor-associated desmoplasia seen in desmoplastic small round cell tumor.
机译:从组织学上讲,增生性小圆形细胞瘤由特征性的肿瘤性小圆形细胞组成,具有分化分化和明显的增生性间质。从遗传学上讲,该肿瘤表现出特征性的11; 22易位,涉及22号染色体上的EWS基因和11号染色体上的WT1基因,产生EWS-WT1融合基因,该基因产生嵌合蛋白,该嵌合蛋白起激活靶基因表达的新型转录因子的作用如PDGF-A。 PDGF-A(一种成纤维细胞的有效生长因子)的表达已在增生性小圆形细胞肿瘤中检测到,并与这些肿瘤的特征性增生相关。作为TGF超家族成员的骨形态发生蛋白在调节细胞生长,分化和骨形成中起着复杂的作用,但尚未在增生性小圆形细胞肿瘤中进行评估。通过标准的免疫组织化学方法,用石蜡上的抗原回收,通过RT-PCR分析确认的总共24例具有EWS-WT1融合产物的增生性小圆形细胞肿瘤的PDGF-A,PDGF-R,TGF3和骨形态发生蛋白-4的表达部分。免疫反应性进行了半定量评估。在苏木精和曙红染色的切片上使用三级量表对与肿瘤相关的增生进行定量。增生性小圆形细胞肿瘤显示与TGF3(21/24),BMP4(14/21),PDGF-A(19/24)和PDGF-R(16/22)具有可变的免疫反应性。基质细胞较不频繁地显示与TGF3,PDGF-R和PDGF-A的反应性。肿瘤相关的异形增生在八个病例中突出,在七个中度,在九个病例中弱。除PDGF-A外,肿瘤相关性增生与所测试的标志物之间没有相关性。与先前的研究相反,我们的研究表明PDGF-A表达水平与肿瘤相关的异型增生呈负相关。除PDGF-A以外,EWS-WT1转录因子的其他靶标可能直接与在增生性小圆形细胞肿瘤中看到的与肿瘤相关的明显增生有关。

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