王旭红, 彭琛, 李乐, 秦彦超. BRAF V600E和TERT启动子突变与甲状腺乳头状癌临床病理特征的关系[J]. 中国肿瘤临床, 2020, 47(11): 557-562. DOI: 10.3969/j.issn.1000-8179.2020.11.358
引用本文: 王旭红, 彭琛, 李乐, 秦彦超. BRAF V600E和TERT启动子突变与甲状腺乳头状癌临床病理特征的关系[J]. 中国肿瘤临床, 2020, 47(11): 557-562. DOI: 10.3969/j.issn.1000-8179.2020.11.358
Wang Xuhong, Chen, Li Le, Qin Yanchao. Relationship between BRAF V600E, TERT promoter mutations and the clinicopathological features of papillary thyroid carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2020, 47(11): 557-562. DOI: 10.3969/j.issn.1000-8179.2020.11.358
Citation: Wang Xuhong, Chen, Li Le, Qin Yanchao. Relationship between BRAF V600E, TERT promoter mutations and the clinicopathological features of papillary thyroid carcinoma[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2020, 47(11): 557-562. DOI: 10.3969/j.issn.1000-8179.2020.11.358

BRAF V600E和TERT启动子突变与甲状腺乳头状癌临床病理特征的关系

Relationship between BRAF V600E, TERT promoter mutations and the clinicopathological features of papillary thyroid carcinoma

  • 摘要:
      目的  探讨端粒酶逆转录酶(telomerase reverse transcriptase,TERT)启动子突变和BRAF V600E突变与甲状腺乳头状癌(papillarythyroid carcinoma,PTC)临床病理因素的关系。
      方法  对2014年12月至2016年12月山西省肿瘤医院728例PTC患者肿瘤组织提取DNA,检测其BRAF V600E和TERT启动子突变情况,收集患者临床病理资料,进行统计学分析。
      结果  728例患者中BRAF V600E突变型308例(42.3%)。TERT C228T突变型78例(10.7%),TERT C250T突变型4例(0.5%)。TERT启动子突变与患者发病年龄(P=0.034)、腺外侵犯(P=0.026)、肿瘤直径(P=0.028)、中央区淋巴结转移(P=0.012)、远处转移(P=0.001)、TNM分期(P < 0.001)、病理亚型(P=0.003)以及肿瘤复发(P=0.002)显著相关。BRAF V600E突变与PTC患者的腺外侵犯(P=0.001)、肿瘤直径(P < 0.001)、桥本甲状腺炎(P < 0.001)、远处转移(P=0.010)、TNM分期(P=0.009)和肿瘤复发(P=0.001)显著相关。同时伴有BRAF V600E和TERT启动子突变与发病年龄(P=0.024)、腺外侵犯(P=0.022)、合并桥本甲状腺炎(P=0.005)、中央区淋巴结转移(P=0.018)及更高临床分期(P=0.002)显著相关。
      结论  V600E和TERT启动子突变与高侵袭性的临床病理因素相关,BRAF V600E和TERT存在协同作用,对于指导治疗和评估预后具有积极作用。

     

    Abstract:
      Objective  To explore the relationship between TERT promoter mutations and BRAF V600E as well as their coexistence with the clinicopathological features of papillary thyroid cancer (PTC).
      Methods  A total of 728 patients enrolled in Shanxi Cancer Hospital from December 2014 to December 2016 with PTC were retrospectively analyzed. We reviewed and analyzed the clinical results, pathology records, ultrasound results, and BRAF V600E and TERT status.
      Results  BRAF V600E mutations were found in 42.3% (308 of 728) of patients, and TERT C228T and C250T promoter mutations were found in 10.7% (78 of 728) and 0.5% (4 of 728) of patients, respectively. The TERT promoter mutation was significantly associated with old age (P=0.034), extrathyroidal invasion (P=0.026), large tumor size (P=0.028), cervical lymph node metastasis (P=0.012), distant metastasis (P=0.001), advanced disease stages (P < 0.001), histological type (P=0.003) and recurrence (P=0.002). The BRAF V600E mutation was significantly associated with extrathyroidal invasion (P=0.001), large tumor size (P < 0.001), Hashimoto thyroiditis (P < 0.001), distant metastasis (P=0.010), advanced disease stages (P=0.009) and recurrence (P=0.001). The coexistence of BRAF V600E and TERT promoter mutations was particularly associated with high-risk clinicopathological features, such as old age (P=0.024), extrathyroidal invasion (P=0.022), Hashimoto thyroiditis (P=0.005), the cervical lymph node (P=0.018), and advanced disease stages (P=0.002).
      Conclusion  Our study demonstrates that BRAF V600E and TERT promoter mutations play a significant role in the aggressiveness of PTC, particularly when the two mutations coexist. The results reveal the significant role of these mutations in the treatment and prognosis prediction of PTC.

     

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