Department of Pathology, University of British Columbia, Vancouver, BC V5Z 1M9, Canada.
British Columbia Cancer Agency, Vancouver, BC V5Z 1L3, Canada.
Neoplasia. 2019 Aug;21(8):740-751. doi: 10.1016/j.neo.2019.05.004. Epub 2019 Jun 17.
Myxoid liposarcoma is a malignant lipogenic tumor that develops in deep soft tissues. While local control rates are good, current chemotherapy options remain ineffective against metastatic disease. Myxoid liposarcoma is characterized by the FUS-DDIT3 fusion oncoprotein that is proposed to function as an aberrant transcription factor, but its exact mechanism of action has remained unclear. To identify the key functional interacting partners of FUS-DDIT3, this study utilized immunoprecipitation-mass spectrometry (IP-MS) to identify the FUS-DDIT3 interactome in whole cell lysates of myxoid liposarcoma cells, and results showed an enrichment of RNA processing proteins. Further quantitative MS analyses of FUS-DDIT3 complexes isolated from nuclear lysates showed that members of several chromatin regulatory complexes were present in the FUS-DDIT3 interactome, including NuRD, SWI/SNF, PRC1, PRC2, and MLL1 COMPASS-like complexes. Co-immunoprecipitation validated the associations of FUS-DDIT3 with BRG1/SMARCA4, BAF155/SMARCC1, BAF57/SMARCE1, and KDM1A. Data from this study provides candidates for functional validation as potential therapeutic targets, particularly for emerging epigenetic drugs.
黏液样脂肪肉瘤是一种发生在深部软组织中的恶性脂肪源性肿瘤。虽然局部控制率良好,但目前的化疗选择对转移性疾病仍然无效。黏液样脂肪肉瘤的特征是存在 FUS-DDIT3 融合癌蛋白,该蛋白被认为是一种异常转录因子,但确切的作用机制仍不清楚。为了鉴定 FUS-DDIT3 的关键功能相互作用伙伴,本研究利用免疫沉淀-质谱(IP-MS)在黏液样脂肪肉瘤细胞的全细胞裂解物中鉴定 FUS-DDIT3 的相互作用组,结果显示 RNA 处理蛋白富集。进一步对核裂解物中分离的 FUS-DDIT3 复合物进行定量 MS 分析表明,几个染色质调节复合物的成员存在于 FUS-DDIT3 相互作用组中,包括 NuRD、SWI/SNF、PRC1、PRC2 和 MLL1 COMPASS 样复合物。共免疫沉淀验证了 FUS-DDIT3 与 BRG1/SMARCA4、BAF155/SMARCC1、BAF57/SMARCE1 和 KDM1A 的关联。本研究的数据为功能验证提供了候选对象,作为潜在的治疗靶点,特别是对于新兴的表观遗传药物。