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滑膜肉瘤发生发展过程中SS18-SSX1与miR-214之间的协同作用。

Cooperation between SS18-SSX1 and miR-214 in Synovial Sarcoma Development and Progression.

作者信息

Tanaka Miwa, Homme Mizuki, Yamazaki Yukari, Ae Keisuke, Matsumoto Seiichi, Subramanian Subbaya, Nakamura Takuro

机构信息

Division of Carcinogenesis, The Cancer Institute, Japanese Foundation for Cancer Research, Tokyo 135-8550, Japan.

Department of Orthopedic Oncology, The Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo 135-8550, Japan.

出版信息

Cancers (Basel). 2020 Jan 30;12(2):324. doi: 10.3390/cancers12020324.

Abstract

SS18-SSX fusion proteins play a central role in synovial sarcoma development, although, the genetic network and mechanisms of synovial sarcomagenesis remain unknown. We established a new ex vivo synovial sarcoma mouse model through retroviral-mediated gene transfer of into mouse embryonic mesenchymal cells followed by subcutaneous transplantation into nude mice. This approach successfully induced subcutaneous tumors in 100% recipients, showing invasive proliferation of short spindle tumor cells with occasional biphasic appearance. Cytokeratin expression was observed in epithelial components in tumors and expression of TLE1 and BCL2 was also shown. Gene expression profiling indicated SWI/SNF pathway modulation by introduction into mesenchymal cells and and upregulation in tumors. These findings indicate that the model exhibits phenotypes typical of human synovial sarcoma. Retroviral tagging of the tumor identified 15 common retroviral integration sites within the locus as the most frequent in 30 mouse synovial sarcomas. and upregulation within the locus was observed. and cointroduction accelerated sarcoma onset, indicating that is a cooperative oncomiR in synovial sarcomagenesis. functions in a cell non-autonomous manner, promoting cytokine gene expression (e.g., ). Our results emphasize the role of in tumor development and disease progression.

摘要

SS18-SSX融合蛋白在滑膜肉瘤的发生发展中起核心作用,尽管滑膜肉瘤发生的遗传网络和机制仍不清楚。我们通过逆转录病毒介导的基因转移,将其导入小鼠胚胎间充质细胞,然后皮下移植到裸鼠体内,建立了一种新的滑膜肉瘤体外小鼠模型。这种方法在100%的受体中成功诱导出皮下肿瘤,显示出短梭形肿瘤细胞的侵袭性增殖,偶尔出现双相外观。在肿瘤的上皮成分中观察到细胞角蛋白表达,同时也显示了TLE1和BCL2的表达。基因表达谱分析表明,将其导入间充质细胞可调节SWI/SNF途径,且在肿瘤中上调。这些发现表明该模型表现出典型人类滑膜肉瘤的表型。对肿瘤进行逆转录病毒标记,在30个小鼠滑膜肉瘤中,确定位于该位点的15个常见逆转录病毒整合位点是最常见的。观察到该位点内的上调。与共导入加速了肉瘤的发生,表明在滑膜肉瘤发生中是一种协同致癌miR。以细胞非自主方式发挥作用,促进细胞因子基因表达(如)。我们的结果强调了在肿瘤发展和疾病进展中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b65/7072427/fe8a8c0e1e18/cancers-12-00324-g001.jpg

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