Nakamura Takuro, Tanaka Miwa
Dept. of Experimental Pathology, Institute of Medical Science, Tokyo Medical University.
Gan To Kagaku Ryoho. 2024 Jun;51(6):585-590.
Alveolar soft part sarcoma(ASPS)is a rare malignant tumor whose origin is unidentified, arising from deep soft tissue and affecting adolescents and young adults. ASPS is characterized by its abundant vascular network forming alveolar structures, and demonstrates frequent hematogenous metastasis. An ASPSCR1-TFE3 fusion gene derived from t(X;17)chromosome translocation is detected as a disease gene in all cases, and the ASPSCR1-TFE3 protein causes abnormal transcriptional regulation. We generated a mouse model for ASPS by introducing ASPSCR1-TFE3 into mouse embryonic mesenchymal cells. In the model, tumor angiogenesis and alveolar structures of human ASPS were reproduced, revealing pericyte-rich blood vessels and metastatic processes with pericytic encapsulation of tumor cell nests. ASPSCR1-TFE3 is frequently associated with active enhancers and super-enhancers, and angiogenesis-related enhancers were significantly diminished by the loss of ASPSCR1- TFE3. Angiogenesis-associated enhancers and important target genes, Rab27a, Sytl2, Pdgfb and Vwf were identified by epigenetic CRISPR screening. Rab27a and Sytl2 facilitates trafficking of cytoplasmic vesicles containing angiogenic factors such as Pdgfb and Vwf, resulting in pericyte-rich vascular structures in ASPS. These studies highlight the importance of the Rab27/Sytl axis as a novel drug target in cancer.
肺泡软组织肉瘤(ASPS)是一种起源不明的罕见恶性肿瘤,起源于深部软组织,主要影响青少年和年轻成年人。ASPS的特征是其丰富的血管网络形成肺泡结构,并常发生血行转移。在所有病例中均检测到源自t(X;17)染色体易位的ASPSCR1-TFE3融合基因作为致病基因,且ASPSCR1-TFE3蛋白会导致异常的转录调控。我们通过将ASPSCR1-TFE3导入小鼠胚胎间充质细胞中建立了ASPS小鼠模型。在该模型中,重现了人类ASPS的肿瘤血管生成和肺泡结构,揭示了富含周细胞的血管以及肿瘤细胞巢被周细胞包裹的转移过程。ASPSCR1-TFE3常与活性增强子和超级增强子相关,并且ASPSCR1-TFE3的缺失会显著减少血管生成相关增强子。通过表观遗传CRISPR筛选鉴定了血管生成相关增强子和重要靶基因Rab27a、Sytl2、Pdgfb和Vwf。Rab27a和Sytl2促进含有血管生成因子如Pdgfb和Vwf的细胞质囊泡的运输,从而在ASPS中形成富含周细胞的血管结构。这些研究突出了Rab27/Sytl轴作为癌症新药物靶点的重要性。