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Retinoblastoma gene abnormalities in early laryngeal cancer.

机译:早期喉癌中的视网膜母细胞瘤基因异常。

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The retinoblastoma gene (Rb) is postulated to be important in carcinoma of the larynx. Its cellular protein (pRb) is involved in regulation of the cell cycle and may be influential in the cells response to irradiation injury. From the University of Liverpool Head and Neck Database we identified 35 patients with a T2 N0 laryngeal squamous carcinoma whom received primary irradiation and had a minimum of 5 years follow up. Laser capture microdissection was performed on paired normal and tumour biopsy material to analyse for loss of heterozygosity (LOH) and microsatellite instability (MI) of the Rb gene and immunohistochemistry (IHC) was carried out to detect pRb expression. Of 35 tumours, 13 were normal, 12 had MI and 5 had LOH of the Rb gene. Abnormalities at the Rb locus did not correlate with loss of pRb expression. There was also no significant difference between the distribution of normal and abnormal gene sequences and whether or not the primary laryngeal tumour recurred after radiotherapy. Rb gene abnormalities occurred in one third of T2 N0 laryngeal carcinomas. These were not in isolation predictive of cure by radiotherapy.
机译:视网膜母细胞瘤基因(Rb)被认为在喉癌中很重要。它的细胞蛋白(pRb)参与细胞周期的调节,并且可能在细胞对辐射损伤的反应中具有影响力。从利物浦大学头颈大学数据库中,我们确定了35例接受T2 N0喉鳞状细胞癌的患者,他们接受了一次初次照射,并至少接受了5年的随访。在配对的正常和肿瘤活检材料上进行激光捕获显微切割,以分析Rb基因的杂合性(LOH)丢失和微卫星不稳定性(MI),并进行免疫组织化学(IHC)检测pRb表达。在35个肿瘤中,有13个是正常肿瘤,有12个患有MI,有5个具有Rb基因的LOH。 Rb基因座的异常与pRb表达的丧失无关。正常和异常基因序列的分布与放疗后是否复发原发性喉癌之间也没有显着差异。 Rb基因异常发生在三分之一的T2 N0喉癌中。这些并非孤立地预示了放射治疗的治愈。

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