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Release the ballast: Glioblastoma rises above radiation therapy by exporting miR-603 in extracellular vesicles to become treatment-resistant

机译:释放镇流器:通过在细胞外囊泡中出口miR-603来抗辐射治疗胶质母细胞瘤以成为抗性的辐射治疗

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Glioblastoma (GBM) remains an incurable disease with a mediansurvival of ~15-18 months post-diagnosis, despite ongoing efforts toimprove treatment outcome [1]. Standard-of-care consists of maximumsafe surgical resection followed by systemic temozolomide (TMZ) andlocal radiation. After initial treatment with this regimen, GBM universally recurs and subsequent lines of therapy have limited efficacy. As aresult, there is a great need to understand the biology of acquired therapeutic resistance in this disease. One mechanism that has been proposed to confer GBM treatment unresponsiveness and recurrence isenrichment of cancer stem cells (CSCs), a population that is resistant tostandard-of-care therapies and has the capacity to give rise to therecurrent tumor. In this issue, Ramakrishnan et al. report that GBMacquires a treatment-resistant CSC phenotype following radiation therapy by actively exporting miR-603 in extracellular vesicles (EV) [2].
机译:尽管持续努力进行治疗结果,但胶质母细胞瘤(GBM)仍然是诊断后〜15-18个月的不治区疾病[1]。护理标准由最高级外科手术切除,然后是全身替代毒物(TMZ)和本地辐射。在用这种方案初始治疗后,GBM普遍丧失和随后的治疗疗效有限。作为遗产,很有需要了解这种疾病中获得的治疗性的生物学。已经提出的一种机制,用于赋予GBM治疗的癌症干细胞(CSC)的癌症干细胞(CSC),耐受护理疗法的群体,并且具有引起肿瘤的能力。在这个问题中,Ramakrishnan等人。通过主动出口细胞外囊泡(EV)[2],通过主动出口miR-603,报告GBMACQUIRE在放射治疗后治疗抗性CSC表型。

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