首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Proteomics of the radioresistant phenotype in head-and-neck cancer: Gp96 as a novel prediction marker and sensitizing target for radiotherapy.
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Proteomics of the radioresistant phenotype in head-and-neck cancer: Gp96 as a novel prediction marker and sensitizing target for radiotherapy.

机译:头颈癌中放射抗性表型的蛋白质组学:Gp96作为放射治疗的新型预测标记和致敏靶标。

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摘要

PURPOSE: Radiotherapy is an integral part of the treatment modality for head-neck cancer (HNC), but in some cases the disease is radioresistant. We designed this study to identify molecules that may be involved in this resistance. METHODS AND MATERIALS: Two radioresistant sublines were established by fractionated irradiation of the HNC cell lines, to determine differentially proteins between parental and radioresistant cells. Proteomic analysis and reverse-transcription polymerase chain reaction were used to identify and confirm the differential proteins. The siRNA knockdown experiments were applied to examine cellular functions of a radioresistant gene, with investigation of the alterations in colonogenic survival, cell cycle status, and reactive oxygen species levels. Xenografted mouse tumors were studied to validate the results. RESULTS: IN all, 64 proteins were identified as being potentially associated with radioresistance, which are involved in several cellular pathways, including regulation of stimulus response, cell apoptosis, and glycolysis. Six genes were confirmed to be differentially expressed in both radioresistant sublines, with Gp96, Grp78, HSP60, Rab40B, and GDF-15 upregulated, and annexin V downregulated. Gp96 was further investigated for its functions in response to radiation. Gp96-siRNA transfectants displayed a radiation-induced growth delay, reduction in colonogenic survival, increased cellular reactive oxygen species levels, and increased proportion of the cells in the G2/M phase. Xenograft mice administered Gp96-siRNA showed significantly enhanced growth suppression in comparison with radiation treatment alone (p = 0.009). CONCLUSIONS: We identified 64 proteins and verified 6 genes that are potentially involved in the radioresistant phenotype. We further demonstrated that Gp96 knockdown enhances radiosensitivity both in cells and in vivo, which may lead to a better prognosis of HNC treatment.
机译:目的:放射疗法是头颈癌(HNC)治疗方法不可或缺的一部分,但在某些情况下,该疾病具有放射抵抗力。我们设计了这项研究,以鉴定可能与这种抗性有关的分子。方法和材料:通过分步照射HNC细胞系建立了两个抗辐射亚系,以测定亲代和抗辐射细胞之间的差异蛋白。蛋白质组学分析和逆转录聚合酶链反应用于鉴定和确认差异蛋白。 siRNA敲低实验用于检查抗辐射基因的细胞功能,并调查结肠存活,细胞周期状态和活性氧水平的变化。研究异种移植的小鼠肿瘤以验证结果。结果:总共鉴定出64种可能与放射抗性相关的蛋白,这些蛋白与多种细胞途径有关,包括调节刺激反应,细胞凋亡和糖酵解。证实六个基因在两个抗辐射亚系中差异表达,其中Gp96,Grp78,HSP60,Rab40B和GDF-15上调,膜联蛋白V下调。进一步研究了Gp96对辐射的反应功能。 Gp96-siRNA转染子显示出辐射诱导的生长延迟,结肠成活率降低,细胞活性氧水平升高以及G2 / M期细胞比例增加。与单独的放射治疗相比,给予Gp96-siRNA的异种移植小鼠显示出显着增强的生长抑制(p = 0.009)。结论:我们鉴定了64种蛋白质并验证了​​6种可能与放射抗性表型有关的基因。我们进一步证明,Gp96基因敲低可增强细胞和体内的放射敏感性,这可能导致HNC治疗的更好预后。

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