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在一种新的血管肉瘤小鼠模型中,联合抑制mTOR和MEK是一种有效的治疗方法。

Combined mTOR and MEK inhibition is an effective therapy in a novel mouse model for angiosarcoma.

作者信息

Chadwick Michelle L, Lane Adam, Thomas Dana, Smith Amanda R, White Angela R, Davidson Dominique, Feng Yuxin, Boscolo Elisa, Zheng Yi, Adams Denise M, Gupta Anita, Veillette André, Chow Lionel M L

机构信息

Department of Cancer and Cell Biology, University of Cincinnati, Cincinnati, OH, USA.

Cancer and Blood Diseases Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.

出版信息

Oncotarget. 2018 May 15;9(37):24750-24765. doi: 10.18632/oncotarget.25345.

DOI:10.18632/oncotarget.25345
PMID:29872503
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5973867/
Abstract

Angiosarcoma is an aggressive malignancy of vascular origin that occurs or in the context of previous cancer therapy. Despite multi-modal aggressive treatment including surgical resection, chemotherapy, and radiation, five-year overall survival remains poor at 35%. Due to its rarity, little is known about its molecular pathology and clinical trials have been extremely difficult to conduct. Development of animal models for rare diseases like angiosarcoma is critical to improve our understanding of tumorigenesis and to test novel treatment regimens. A genetically engineered mouse model for angiosarcoma was generated by conditional deletion of , , and in endothelial cells. Tumors arising from these mice recapitulate the histology and molecular pathology of the human disease including hyperactivation of the PI3K/mTOR and MAPK signaling pathways. Treatment of tumor-bearing mice with mTOR or MEK inhibitors effectively inactivated signaling and resulted in reduced proliferation and elevated apoptosis leading to tumor regression. The effect of treatment on tumor growth was transient and proliferation was restored after a period of dormancy. However, combined inhibition of mTOR and MEK resulted in profound tumor regression which was sustained for the duration of treatment. These results suggest that angiosarcoma may be effectively treated by this drug combination. .

摘要

血管肉瘤是一种起源于血管的侵袭性恶性肿瘤,可发生于既往有癌症治疗史的背景下。尽管采取了包括手术切除、化疗和放疗在内的多模式积极治疗,但五年总生存率仍很低,仅为35%。由于其罕见性,对其分子病理学知之甚少,开展临床试验也极其困难。开发像血管肉瘤这样的罕见疾病的动物模型对于增进我们对肿瘤发生的理解以及测试新的治疗方案至关重要。通过在内皮细胞中条件性缺失、和,构建了一种血管肉瘤的基因工程小鼠模型。这些小鼠产生的肿瘤重现了人类疾病的组织学和分子病理学,包括PI3K/mTOR和MAPK信号通路的过度激活。用mTOR或MEK抑制剂治疗荷瘤小鼠可有效使信号失活,导致增殖减少和凋亡增加,从而使肿瘤消退。治疗对肿瘤生长的影响是短暂的,休眠一段时间后增殖恢复。然而,联合抑制mTOR和MEK导致肿瘤深度消退,并在治疗期间持续存在。这些结果表明,这种药物联合可能有效治疗血管肉瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b38a/5973867/745bf1fb0032/oncotarget-09-24750-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b38a/5973867/28b9e4d8af2a/oncotarget-09-24750-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b38a/5973867/2e2b1494b00c/oncotarget-09-24750-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b38a/5973867/55e0dd6074c5/oncotarget-09-24750-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b38a/5973867/9aba14a60a80/oncotarget-09-24750-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b38a/5973867/745bf1fb0032/oncotarget-09-24750-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b38a/5973867/28b9e4d8af2a/oncotarget-09-24750-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b38a/5973867/2e2b1494b00c/oncotarget-09-24750-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b38a/5973867/55e0dd6074c5/oncotarget-09-24750-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b38a/5973867/9aba14a60a80/oncotarget-09-24750-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b38a/5973867/745bf1fb0032/oncotarget-09-24750-g005.jpg

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