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BRAF和TERT启动子突变与甲状腺乳头状癌侵袭性的关系:653例患者的研究

BRAF and TERT promoter mutations in the aggressiveness of papillary thyroid carcinoma: a study of 653 patients.

作者信息

Jin Langping, Chen Endong, Dong Siyang, Cai Yefeng, Zhang Xiangjian, Zhou Yili, Zeng Ruichao, Yang Fan, Pan Chuanmeng, Liu Yehuan, Wu Weili, Xing Mingzhao, Zhang Xiaohua, Wang Ouchen

机构信息

Department of Surgical Oncology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang Province 325000, China.

Department of Surgical Oncology, The Third Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang Province 325000, China.

出版信息

Oncotarget. 2016 Apr 5;7(14):18346-55. doi: 10.18632/oncotarget.7811.

Abstract

The role of telomerase reverse transcriptase (TERT) gene promoter mutations in the aggressiveness of papillary thyroid cancer (PTC) remains to be further investigated. Here we examined the relationship of TERT promoter mutations and BRAF V600E with the clinicopathological features of PTC in 653 patients. Sanger sequencing of genomic DNA from primary PTC tumors was performed for mutation detection and genotype-clinicopathological correlation of the tumor was analyzed. BRAF V600E and TERT promoter mutations were found in 63.7% (416 of 653) and 4.1% (27 of 653) of patients, respectively; the latter became 9.8% when only tumors ≥ 1.5 cm were analyzed. TERT promoter mutations occurred more frequently in BRAF mutation-positive cases compared to wild-type cases, being 5.3% in the former versus 2.1% in the latter (P = 0.050). BRAF and TERT promoter mutations were each significantly associated with high-risk clinicopathological features of PTC, such as old patient age, large tumor size, extrathyroidal invasion, capsular invasion, and advanced disease stages. Coexistence of BRAF V600E and TERT promoter mutations was particularly associated with high-risk clinicopathological features, as exemplified by extrathyroidal invasion seen in 54.5% (12/22) of patients harboring both mutations versus 9.9% (23/232) of patients harboring neither mutation (P < 0.001). Thus, this study, the largest on TERT mutation so far, demonstrates a significant role of BRAF V600E and TERT promoter mutations in the aggressiveness of PTC, which is particularly robust and cooperative when the two mutations coexist. These results, together with previous studies, establish a significant role of these mutations in the aggressiveness of PTC.

摘要

端粒酶逆转录酶(TERT)基因启动子突变在甲状腺乳头状癌(PTC)侵袭性中的作用仍有待进一步研究。在此,我们研究了653例患者中TERT启动子突变和BRAF V600E与PTC临床病理特征的关系。对原发性PTC肿瘤的基因组DNA进行桑格测序以检测突变,并分析肿瘤的基因型与临床病理的相关性。BRAF V600E和TERT启动子突变分别在63.7%(653例中的416例)和4.1%(653例中的27例)的患者中被发现;仅分析≥1.5 cm的肿瘤时,后者比例变为9.8%。与野生型病例相比,TERT启动子突变在BRAF突变阳性病例中更频繁发生,前者为5.3%,后者为2.1%(P = 0.050)。BRAF和TERT启动子突变均与PTC的高风险临床病理特征显著相关,如患者年龄较大、肿瘤体积大、甲状腺外侵犯、包膜侵犯和疾病晚期。BRAF V600E和TERT启动子突变共存尤其与高风险临床病理特征相关,例如在同时携带两种突变的患者中有54.5%(12/22)出现甲状腺外侵犯,而在两种突变均未携带的患者中为9.9%(23/232)(P < 0.001)。因此,这项迄今为止关于TERT突变的最大规模研究表明,BRAF V600E和TERT启动子突变在PTC侵袭性中起重要作用,当两种突变共存时这种作用尤为显著且协同。这些结果与先前的研究一起,证实了这些突变在PTC侵袭性中的重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf6a/4951292/f8148d718061/oncotarget-07-18346-g001.jpg

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