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肌苷 5'-单磷酸脱氢酶 II 型的过表达介导人骨肉瘤细胞对化疗的耐药性。

Overexpression of inosine 5'-monophosphate dehydrogenase type II mediates chemoresistance to human osteosarcoma cells.

机构信息

Department of Experimental Orthopedics, Orthopedic University Hospital Heidelberg, Heidelberg, Germany.

出版信息

PLoS One. 2010 Aug 16;5(8):e12179. doi: 10.1371/journal.pone.0012179.

Abstract

BACKGROUND

Chemoresistance is the principal reason for poor survival and disease recurrence in osteosarcoma patients. Inosine 5'-monophosphate dehydrogenase type II (IMPDH2) encodes the rate-limiting enzyme in the de novo guanine nucleotide biosynthesis and has been linked to cell growth, differentiation, and malignant transformation. In a previous study we identified IMPDH2 as an independent prognostic factor and observed frequent IMPDH2 overexpression in osteosarcoma patients with poor response to chemotherapy. The aim of this study was to provide evidence for direct involvement of IMPDH2 in the development of chemoresistance.

METHODOLOGY/PRINCIPAL FINDINGS: Stable cell lines overexpressing IMPDH2 and IMPDH2 knock-down cells were generated using the osteosarcoma cell line Saos-2 as parental cell line. Chemosensitivity, proliferation, and the expression of apoptosis-related proteins were analyzed by flow cytometry, WST-1-assay, and western blot analysis. Overexpression of IMPDH2 in Saos-2 cells induced strong chemoresistance against cisplatin and methotrexate. The observed chemoresistance was mediated at least in part by increased expression of the anti-apoptotic proteins Bcl-2, Mcl-1, and XIAP, reduced activation of caspase-9, and, consequently, reduced cleavage of the caspase substrate PARP. Pharmacological inhibition of IMPDH induced a moderate reduction of cell viability and a strong decrease of cell proliferation, but no increase in chemosensitivity. However, chemoresistant IMPDH2-overexpressing cells could be resensitized by RNA interference-mediated downregulation of IMPDH2.

CONCLUSIONS

IMPDH2 is directly involved in the development of chemoresistance in osteosarcoma cells, suggesting that targeting of IMPDH2 by RNAi or more effective pharmacological inhibitors in combination with chemotherapy might be a promising means of overcoming chemoresistance in osteosarcomas with high IMPDH2 expression.

摘要

背景

化学耐药性是骨肉瘤患者生存和疾病复发不良的主要原因。肌苷 5'-单磷酸脱氢酶 2(IMPDH2)编码从头嘌呤核苷酸合成中的限速酶,与细胞生长、分化和恶性转化有关。在之前的研究中,我们发现 IMPDH2 是一个独立的预后因素,并观察到对化疗反应不佳的骨肉瘤患者中 IMPDH2 过度表达频繁。本研究旨在为 IMPDH2 直接参与化学耐药性的发展提供证据。

方法/主要发现:使用骨肉瘤细胞系 Saos-2 作为亲本细胞系,生成了过表达 IMPDH2 和 IMPDH2 敲低细胞的稳定细胞系。通过流式细胞术、WST-1 测定和 Western blot 分析分析了化学敏感性、增殖和凋亡相关蛋白的表达。Saos-2 细胞中 IMPDH2 的过表达诱导了对顺铂和甲氨蝶呤的强烈化学耐药性。观察到的化学耐药性至少部分是通过增加抗凋亡蛋白 Bcl-2、Mcl-1 和 XIAP 的表达、降低 caspase-9 的激活以及随后降低半胱天冬酶底物 PARP 的裂解来介导的。IMPDH 的药理学抑制诱导细胞活力适度降低和细胞增殖强烈降低,但化学敏感性没有增加。然而,通过 RNA 干扰介导的 IMPDH2 下调可以使化学耐药性的 IMPDH2 过表达细胞重新敏感。

结论

IMPDH2 直接参与骨肉瘤细胞化学耐药性的发展,提示通过 RNAi 或更有效的药理学抑制剂靶向 IMPDH2 与化疗联合可能是克服高 IMPDH2 表达骨肉瘤化学耐药性的一种有前途的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6a3/2922339/a567ae11629d/pone.0012179.g001.jpg

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