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首页> 外文期刊>British Journal of Cancer >The tumour hypoxia marker pimonidazole reflects a transcriptional programme associated with aggressive prostate cancer
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The tumour hypoxia marker pimonidazole reflects a transcriptional programme associated with aggressive prostate cancer

机译:肿瘤缺氧标记物pimonidazole反映与侵略性前列腺癌相关的转录程序

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Background: The hypoxia marker pimonidazole is a candidate biomarker of cancer aggressiveness. We investigated the transcriptional programme associated with pimonidazole staining in prostate cancer. Methods: Index tumour biopsies were taken by image guidance from an investigation cohort of 52 patients, where 43 patients received pimonidazole before prostatectomy. Biopsy location within the index tumour was verified for 46 (88%) patients, who were included for gene expression profiling and immunohistochemistry. Two independent cohorts of 59 and 281 patients were used for validation. Results: Expression of genes in proliferation, DNA repair and hypoxia response was a major part of the transcriptional programme associated with pimonidazole staining. A signature of 32 essential genes was constructed and showed positive correlation to Ki67 staining, confirming the increased proliferation in hypoxic tumours as suggested from the gene data. Positive correlations were also found to tumour stage and lymph node status, but not to blood prostate-specific antigen level, consistent with the findings for pimonidazole staining. The association with aggressiveness was confirmed in validation cohorts, where the signature correlated with Gleason score and had independent prognostic impact, respectively. Conclusions: Pimonidazole staining reflects an aggressive hypoxic phenotype of prostate cancer characterised by upregulation of proliferation, DNA repair and hypoxia response genes.
机译:背景:低氧标记物pimonidazole是癌症侵袭性的候选生物标记物。我们调查了与吡莫硝唑染色相关的前列腺癌的转录程序。方法:通过对52例患者的研究队列进行图像引导,对活检指标进行活检,其中43例患者在前列腺切除术前接受了吡莫尼唑治疗。证实了46名(88%)患者的活检在索引肿瘤中的位置,这些患者被纳入基因表达谱分析和免疫组化分析。分别使用59和281名患者的两个独立队列进行验证。结果:增殖,DNA修复和缺氧反应中的基因表达是与吡莫硝唑染色有关的转录程序的主要部分。构建了32个必需基因的签名,并显示与Ki67染色呈正相关,从而证实了低氧肿瘤中增殖的增加(如基因数据所示)。还发现与肿瘤分期和淋巴结状态呈正相关,但与血液前列腺特异性抗原水平无正相关,这与吡莫硝唑染色的结果一致。在验证队列中证实了与攻击性的关联,其中签名与格里森评分相关并且分别具有独立的预后影响。结论:吡莫尼唑染色反映了前列腺癌的一种侵袭性低氧表型,其特征在于增殖,DNA修复和缺氧反应基因的上调。

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