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CD44 有助于调节骨肉瘤中 MDR1 蛋白和多柔比星化疗耐药性。

CD44 Contributes to the Regulation of MDR1 Protein and Doxorubicin Chemoresistance in Osteosarcoma.

机构信息

Department of Medicine I, University Medical Center of the Johannes Gutenberg University, 55131 Mainz, Germany.

Leibniz Institute on Aging-Fritz Lipmann Institute (FLI), 07745 Jena, Germany.

出版信息

Int J Mol Sci. 2022 Aug 3;23(15):8616. doi: 10.3390/ijms23158616.

Abstract

Osteosarcoma is the most common type of pediatric bone tumor. Despite great advances in chemotherapy during the past decades, the survival rates of osteosarcoma patients remain unsatisfactory. Drug resistance is one of the main reasons, leading to treatment failure and poor prognosis. Previous reports correlated expression of cluster of differentiation 44 (CD44) with drug resistance and poor survival of osteosarcoma patients, however the underlying mechanisms are poorly defined. Here, we investigated the role of CD44 in the regulation of drug chemoresistance, using osteosarcoma cells isolated from mice carrying a mutation of the tumor suppressor neurofibromatosis type 2 () gene. CD44 expression was knocked-down in the cells using CRISPR/Cas9 approach. Subsequently, CD44 isoforms and mutants were re-introduced to investigate CD44-dependent processes. Sensitivity to doxorubicin was analyzed in the osteosarcoma cells with modified CD44 expression by immunoblot, colony formation- and WST-1 assay. To dissect the molecular alterations induced by deletion of , RNA sequencing was performed on -positive and -negative primary osteosarcoma tissues isolated from -mutant mice. Subsequently, expression of candidate genes was evaluated by quantitative reverse transcription PCR (qRT-PCR). Our results indicate that CD44 increases the resistance of osteosarcoma cells to doxorubicin by up-regulating the levels of multidrug resistance (MDR) 1 protein expression, and suggest the role of proteolytically released CD44 intracellular domain, and hyaluronan interactions in this process. Moreover, high throughput sequencing analysis identified differential regulation of several apoptosis-related genes in -positive and -negative primary osteosarcomas, including p53 apoptosis effector related to PMP-22 (). Deletion of in osteosarcoma cells led to doxorubicin-dependent p53 activation and a profound increase in mRNA expression. Overall, our results suggest that CD44 might be an important regulator of drug resistance and suggest that targeting CD44 can sensitize osteosarcoma to standard chemotherapy.

摘要

骨肉瘤是最常见的儿童骨肿瘤类型。尽管在过去几十年中化疗取得了巨大进展,但骨肉瘤患者的生存率仍不尽人意。耐药性是导致治疗失败和预后不良的主要原因之一。先前的报告表明,CD44 的表达与骨肉瘤患者的耐药性和生存率降低相关,但潜在机制尚不清楚。在这里,我们使用携带肿瘤抑制基因神经纤维瘤病 2 突变的小鼠分离的骨肉瘤细胞,研究了 CD44 在调节药物化疗耐药中的作用。使用 CRISPR/Cas9 方法敲低细胞中的 CD44 表达。随后,通过引入 CD44 同工型和突变体来研究 CD44 依赖性过程。通过免疫印迹、集落形成和 WST-1 测定分析了具有修饰的 CD44 表达的骨肉瘤细胞对阿霉素的敏感性。为了剖析 缺失引起的分子变化,对从 -突变小鼠中分离的 -阳性和 -阴性原发性骨肉瘤组织进行了 RNA 测序。随后,通过定量逆转录 PCR(qRT-PCR)评估候选基因的表达。我们的结果表明,CD44 通过上调多药耐药 (MDR) 1 蛋白表达水平增加骨肉瘤细胞对阿霉素的耐药性,并提示在该过程中,蛋白水解释放的 CD44 细胞内结构域和透明质酸相互作用的作用。此外,高通量测序分析鉴定了 -阳性和 -阴性原发性骨肉瘤中几种与凋亡相关的基因的差异调节,包括与 PMP-22 相关的 p53 凋亡效应物()。骨肉瘤细胞中 缺失导致阿霉素依赖性 p53 激活和 mRNA 表达的显著增加。总体而言,我们的结果表明 CD44 可能是药物耐药性的重要调节剂,并表明靶向 CD44 可以使骨肉瘤对标准化疗敏感。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c22/9368984/a9e4618622e3/ijms-23-08616-g001.jpg

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