诱导成肌细胞分化可提高软组织肉瘤细胞系中耐药细胞的化疗敏感性

Q2 Medicine Sarcoma Pub Date : 2020-03-26 eCollection Date: 2020-01-01 DOI:10.1155/2020/8647981
Lucy E Dawson, Luca D'Agostino, Abraham A Hakim, Richard D Lackman, Spencer A Brown, Richard B Sensenig, Zeus A Antonello, Igor I Kuzin
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引用次数: 0

摘要

横纹肌肉瘤(RMS)和横纹肌样瘤(RT)是罕见的软组织恶性肿瘤,在婴儿、儿童和青少年中发病率最高。晚期、复发性和/或转移性横纹肌肉瘤和横纹肌样瘤对治疗的反应较差。瘤内异质性被认为是耐药性背后的主要机制之一。在这项研究中,我们调查了胚胎型RMS(ERMS)细胞系和RT细胞系中的肌原决定因子1(MYOD1)和Noggin(NOG)标记物,以及表达MYOD1和NOG的亚群对化疗的不同反应。重要的是,我们发现这些标记共同确定了一个细胞亚群(MYOD1+ NOG+细胞),该亚群对长春新碱和多柔比星这两种治疗ERMS和RT的常用化疗药物具有原发性耐药性。耐化疗的 MYOD1+ NOG+ 细胞表达未分化细胞的标记,如肌原蛋白和 ID1。长春新碱与TPA/GSK126--一种被证明能诱导RMS细胞系分化的药物组合--相结合,能部分克服MYOD1/NOG细胞的化疗耐药性。
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Induction of Myogenic Differentiation Improves Chemosensitivity of Chemoresistant Cells in Soft-Tissue Sarcoma Cell Lines.

Rhabdomyosarcoma (RMS) and rhabdoid tumors (RT) are rare soft-tissue malignancies with the highest incidence in infants, children, and adolescents. Advanced, recurrent, and/or metastatic RMS and RT exhibit poor response to treatment. One of the main mechanisms behind resistance to treatment is believed to be intratumoral heterogeneity. In this study, we investigated the myogenic determination factor 1 (MYOD1) and Noggin (NOG) markers in an embryonal RMS (ERMS) cell line and an RT cell line and the differential response of the MYOD1 and NOG expressing subpopulations to chemotherapy. Importantly, we found that these markers together identify a subpopulation of cells (MYOD1+ NOG+ cells) with primary resistance to Vincristine and Doxorubicin, two commonly used chemotherapies for ERMS and RT. The chemoresistant MYOD1+ NOG+ cells express markers of undifferentiated cells such as myogenin and ID1. Combination of Vincristine with TPA/GSK126, a drug combination shown to induce differentiation of RMS cell lines, is able to partially overcome MYOD1/NOG cells chemoresistance.

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来源期刊
Sarcoma
Sarcoma Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
5.00
自引率
0.00%
发文量
15
审稿时长
14 weeks
期刊介绍: Sarcoma is dedicated to publishing papers covering all aspects of connective tissue oncology research. It brings together work from scientists and clinicians carrying out a broad range of research in this field, including the basic sciences, molecular biology and pathology and the clinical sciences of epidemiology, surgery, radiotherapy and chemotherapy. High-quality papers concerning the entire range of bone and soft tissue sarcomas in both adults and children, including Kaposi"s sarcoma, are published as well as preclinical and animal studies. This journal provides a central forum for the description of advances in diagnosis, assessment and treatment of this rarely seen, but often mismanaged, group of patients.
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