Institute of Molecular Medicine, Phoenix Children's Hospital, Phoenix, AZ, USA.
Department of Child Health, University of Arizona College of Medicine-Phoenix, Phoenix, AZ, USA.
Mod Pathol. 2021 Apr;34(4):748-757. doi: 10.1038/s41379-020-00719-0. Epub 2020 Dec 9.
Alveolar Rhabdomyosarcoma (ARMS) is an aggressive pediatric cancer with about 80% of cases characterized by either a t(1;13)(p36;q14) or t(2;13)(q35;q14), which results in the formation of the fusion oncogenes PAX7-FOXO1 and PAX3-FOXO1, respectively. Since patients with fusion-positive ARMS (FP-RMS) have a poor prognosis and are treated with an aggressive therapeutic regimen, correct classification is of clinical importance. Detection of the translocation by different molecular methods is used for diagnostics, including fluorescence in situ hybridization and RT-PCR or NGS based approaches. Since these methods are complex and time consuming, we developed specific monoclonal antibodies (mAbs) directed to the junction region on the PAX3-FOXO1 fusion protein. Two mAbs, PFM.1 and PFM.2, were developed and able to immunoprecipitate in vitro-translated PAX3-FOXO1 and cellular PAX3-FOXO1 from FP-RMS cells. Furthermore, the mAbs recognized a 105 kDa band in PAX3-FOXO1-transfected cells and in FP-RMS cell lines. The mAbs did not recognize proteins in fusion-negative embryonal rhabdomyosarcoma cell lines, nor did they recognize PAX3 or FOXO1 alone when compared to anti-PAX3 and anti-FOXO1 antibodies. We next evaluated the ability of mAb PFM.2 to detect the fusion protein by immunohistochemistry. Both PAX3-FOXO1 and PAX7-FOXO1 were detected in HEK293 cells transfected with the corresponding cDNAs. Subsequently, we stained 26 primary tumor sections and a rhabdomyosarcoma tissue array and detected both fusion proteins with a positive predictive value of 100%, negative predictive value of 98%, specificity of 100% and a sensitivity of 91%. While tumors are stained homogenously in PAX3-FOXO1 cases, the staining pattern is heterogenous with scattered positive cells only in tumors expressing PAX7-FOXO1. No staining was observed in stromal cells, embryonal rhabdomyosarcoma, and fusion-negative rhabdomyosarcoma. These results demonstrate that mAbs specific for the chimeric oncoproteins PAX3-FOXO1 and PAX7-FOXO1 can be used efficiently for simple and fast subclassification of rhabdomyosarcoma in routine diagnostics via immunohistochemical detection.
肺泡横纹肌肉瘤(ARMS)是一种侵袭性儿科癌症,约 80%的病例特征为 t(1;13)(p36;q14)或 t(2;13)(q35;q14),分别导致融合癌基因 PAX7-FOXO1 和 PAX3-FOXO1 的形成。由于融合阳性 ARMS(FP-RMS)患者预后不良,并且采用积极的治疗方案进行治疗,因此正确分类具有临床重要性。通过不同的分子方法检测易位用于诊断,包括荧光原位杂交和 RT-PCR 或基于 NGS 的方法。由于这些方法复杂且耗时,因此我们开发了针对 PAX3-FOXO1 融合蛋白连接区的特异性单克隆抗体(mAb)。开发了两种 mAb,PFM.1 和 PFM.2,能够体外翻译的 PAX3-FOXO1 和 FP-RMS 细胞中的细胞 PAX3-FOXO1 进行免疫沉淀。此外,mAb 在转染 PAX3-FOXO1 的细胞和 FP-RMS 细胞系中识别 105 kDa 带。当与抗 PAX3 和抗 FOXO1 抗体相比时,mAb 既不识别融合阴性胚胎横纹肌肉瘤细胞系中的蛋白质,也不单独识别 PAX3 或 FOXO1。接下来,我们评估了 mAb PFM.2 通过免疫组化检测融合蛋白的能力。用相应 cDNA 转染的 HEK293 细胞中均检测到 PAX3-FOXO1 和 PAX7-FOXO1。随后,我们对 26 个原发性肿瘤切片和横纹肌肉瘤组织阵列进行了染色,并以 100%的阳性预测值、98%的阴性预测值、100%的特异性和 91%的敏感性检测到这两种融合蛋白。在 PAX3-FOXO1 病例中,肿瘤均匀染色,而在仅表达 PAX7-FOXO1 的肿瘤中,染色模式呈异质性,仅散布阳性细胞。在基质细胞、胚胎性横纹肌肉瘤和融合阴性横纹肌肉瘤中均未观察到染色。这些结果表明,针对嵌合癌蛋白 PAX3-FOXO1 和 PAX7-FOXO1 的特异性 mAb 可通过免疫组化检测用于横纹肌肉瘤的简单快速亚分类,用于常规诊断。