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甲状腺乳头状癌中BRAF T1796A突变的频率与诊断时患者的年龄有关,而与辐射暴露无关。

Frequency of BRAF T1796A mutation in papillary thyroid carcinoma relates to age of patient at diagnosis and not to radiation exposure.

作者信息

Powell Ned, Jeremiah Steve, Morishita Mariko, Dudley Ed, Bethel Jackie, Bogdanova Tetyana, Tronko Mykola, Thomas Gerry

机构信息

Human Cancer Studies Group, The Clinical School, Swansea University, Singleton Park, Swansea, Wales, UK.

出版信息

J Pathol. 2005 Apr;205(5):558-64. doi: 10.1002/path.1736.

Abstract

In this study, the frequency of BRAF mutation was investigated in a series of 67 cases of papillary thyroid cancer (PTC) in patients from Ukraine. Thirty-two patients were aged 30 years or older at the time of diagnosis and 35 were under 16. Tumour was microdissected from paraffin wax-embedded sections, DNA extracted, and the presence of the BRAF T1796A mutation demonstrated by two different methods: PCR followed by restriction enzyme digestion or primer extension assay and detection using MALDI-TOF mass spectrometry. Eighteen (58%) of the adult cases, but only one of the 35 cases aged less than 16 harboured a BRAF T1796A mutation. There was complete agreement between the two methods used, suggesting that the MALDI-TOF assay is a robust alternative to conventional mutation analysis. RET rearrangement was also examined in the young cohort. The overall frequency of RET rearrangement was 45.7%. Eight of the younger group of patients were born after 1 December 1986 and were therefore not exposed to radioiodine in fallout from Chernobyl. None of the PTCs from these eight patients were positive for BRAF mutation. The frequency of RET rearrangement was 44% in the 27 cases exposed to radiation and 50% in the eight not exposed. These results suggest that the different molecular biological profiles observed are associated with the age of the patient at diagnosis with PTC, rather than being associated with radiation exposure.

摘要

在本研究中,对来自乌克兰的一系列67例甲状腺乳头状癌(PTC)患者的BRAF突变频率进行了调查。32例患者在诊断时年龄为30岁或以上,35例年龄在16岁以下。从石蜡包埋切片中显微切割肿瘤,提取DNA,并通过两种不同方法检测BRAF T1796A突变的存在:PCR后进行限制性酶切或引物延伸分析,并使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF)进行检测。18例(58%)成年病例携带BRAF T1796A突变,但35例16岁以下病例中只有1例携带该突变。所使用的两种方法结果完全一致,表明MALDI-TOF分析是传统突变分析的可靠替代方法。还对年轻队列中的RET重排进行了检测。RET重排的总体频率为45.7%。较年轻组中有8例患者于1986年12月1日后出生,因此未暴露于切尔诺贝利事故沉降物中的放射性碘。这8例患者的PTC中均无BRAF突变阳性。在27例暴露于辐射的病例中,RET重排频率为44%,在8例未暴露的病例中为50%。这些结果表明,观察到的不同分子生物学特征与PTC诊断时患者的年龄相关,而非与辐射暴露相关。

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