Li Jian-Jun, Zheng Ping Chen Jue-Ru, Wang Yao-Zong
Thyroid Surgery, Ningbo No.2 Hospital, No. 41, Xibei Street, Haishu District, Ningbo, 315010, Zhejiang, People's Republic of China.
World J Surg Oncol. 2017 Jun 6;15(1):114. doi: 10.1186/s12957-017-1170-z.
This study aims at exploring the correlations between DNA methylation and polymorphisms in the promoter region of the human telomerase reverse transcriptase (hTERT) gene and postoperative recurrence in patients with thyroid carcinoma (TC).
A total of 312 patients diagnosed with TC were chosen for the study and categorized into recurrence (n = 75) and non-recurrence (n = 237) groups. The hTERT rs2736100 and rs2736098 polymorphisms were detected by performing polymerase chain reaction-restriction fragment length polymorphism. DNA methylation in the promoter region of hTERT gene was evaluated by pyrosequencing. A telephonic and/or outpatient follow-up was conducted for all patients. The correlations of DNA methylation and polymorphisms in the promoter region of hTERT with postoperative recurrence of TC patients underwent analysis.
The patient in the recurrence group showed evidently different pathological types and tumor stages in comparison to the non-recurrence group. The GG genotype of hTERT rs2736100 might increase the recurrence risk of TC patients. No correlations between hTERT rs2736098 polymorphisms and recurrence risk were observed. Compared to the TT + TG genotype frequency, the rs2736100 GG genotype frequency increased in patients without multicentricity, patients with extrathyroidal invasion, patients with lymph node metastasis, patients with undifferentiated carcinoma, and patients in the III + IV stage. The recurrence group showed significantly higher DNA methylation level compared to the non-recurrence group. The DNA methylation level was closely associated to tumor stage and lymph node metastasis of TC patients in the recurrence group.
The DNA methylation and rs2736100 polymorphisms in the promoter region of hTERT gene might be in correlation to postoperative recurrence of TC patients.
本研究旨在探讨人端粒酶逆转录酶(hTERT)基因启动子区域的DNA甲基化与多态性之间的相关性,以及甲状腺癌(TC)患者术后复发情况。
共选取312例诊断为TC的患者进行研究,分为复发组(n = 75)和非复发组(n = 237)。通过聚合酶链反应-限制性片段长度多态性检测hTERT rs2736100和rs2736098多态性。采用焦磷酸测序法评估hTERT基因启动子区域的DNA甲基化。对所有患者进行电话和/或门诊随访。分析hTERT启动子区域DNA甲基化和多态性与TC患者术后复发的相关性。
与非复发组相比,复发组患者的病理类型和肿瘤分期明显不同。hTERT rs2736100的GG基因型可能增加TC患者的复发风险。未观察到hTERT rs2736098多态性与复发风险之间的相关性。与TT + TG基因型频率相比,rs2736100 GG基因型频率在无多中心性、有甲状腺外侵犯、有淋巴结转移、有未分化癌的患者以及III + IV期患者中增加。复发组的DNA甲基化水平明显高于非复发组。复发组中DNA甲基化水平与TC患者的肿瘤分期和淋巴结转移密切相关。
hTERT基因启动子区域的DNA甲基化和rs2736100多态性可能与TC患者术后复发相关。