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外膜线粒体转位酶复合体亚基 20(TOMM20)促进软骨肉瘤的侵袭性和治疗耐药性。

Translocase of the outer mitochondrial membrane complex subunit 20 (TOMM20) facilitates cancer aggressiveness and therapeutic resistance in chondrosarcoma.

机构信息

Department of Medical Oncology, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, USA.

Department of Pharmacology, Division of Biostatistics, Sidney Kimmel Cancer Center, Thomas Jefferson University, Philadelphia, USA.

出版信息

Biochim Biophys Acta Mol Basis Dis. 2020 Dec 1;1866(12):165962. doi: 10.1016/j.bbadis.2020.165962. Epub 2020 Sep 10.

Abstract

Chondrosarcoma is the second most common primary bone malignancy, representing one fourth of all primary bone sarcomas. It is typically resistant to radiation and chemotherapy treatments. However, the molecular mechanisms that contribute to cancer aggressiveness in chondrosarcomas remain poorly characterized. Here, we studied the role of mitochondrial transporters in chondrosarcoma aggressiveness including chemotherapy resistance. Histological grade along with stage are the most important prognostic biomarkers in chondrosarcoma. We found that high-grade human chondrosarcoma tumors have higher expression of the mitochondrial protein, translocase of the outer mitochondrial membrane complex subunit 20 (TOMM20), compared to low-grade tumors. TOMM20 overexpression in human chondrosarcoma cells induces chondrosarcoma tumor growth in vivo. TOMM20 drives proliferation, resistance to apoptosis and chemotherapy resistance. Also, TOMM20 induces markers of epithelial to mesenchymal transition (EMT) and metabolic reprogramming in these mesenchymal tumors. In conclusion, TOMM20 drives chondrosarcoma aggressiveness and resistance to chemotherapy.

摘要

软骨肉瘤是第二常见的原发性骨恶性肿瘤,占所有原发性骨肉瘤的四分之一。它通常对放射治疗和化学疗法治疗有抗性。然而,导致软骨肉瘤侵袭性的分子机制仍未得到充分描述。在这里,我们研究了线粒体转运蛋白在软骨肉瘤侵袭性包括化疗耐药性中的作用。组织学分级以及分期是软骨肉瘤最重要的预后生物标志物。我们发现,与低级别肿瘤相比,高级别人软骨肉瘤肿瘤中线粒体蛋白外膜线粒体转运蛋白复合物亚基 20(TOMM20)的表达更高。人软骨肉瘤细胞中 TOMM20 的过表达会诱导体内软骨肉瘤肿瘤生长。TOMM20 驱动增殖、抗凋亡和化疗耐药性。此外,TOMM20 诱导这些间充质肿瘤中上皮间质转化(EMT)和代谢重编程的标志物。总之,TOMM20 驱动软骨肉瘤侵袭性和化疗耐药性。

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