Relationships of BRAF mutation and HMGB1 to papillary thyroid carcinoma

被引:13
作者
Guan, Xiaolei [1 ]
Wang, Ping [1 ]
Chi, Jingwei [2 ]
Zhao, Shihua [1 ]
Wang, Fei [1 ]
机构
[1] Qingdao Univ, Affiliated Hosp, Dept Endocrinol & Metab, Qingdao 266555, Peoples R China
[2] Qingdao Univ, Affiliated Hosp, Qingdao Key Lab Thyroid Dis, Qingdao 266555, Peoples R China
关键词
Papillary thyroid cancer; BRAF V600E; HMGB1; CANCER CELLS; THERAPEUTIC TARGET; V600E MUTATION; INFLAMMATION; METASTASIS; MECHANISMS; EXPRESSION; RESISTANCE; SURVIVAL; IMPACT;
D O I
10.1016/j.bbrc.2017.03.117
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A poor papillary thyroid cancer (PTC) prognosis is strongly associated with the BRAF V600E mutation. During tumor progression, levels of the high mobility group box 1 (HMGB1) protein are often dysregulated. Results herein demonstrate that HMGB1 protein levels differ between tumor and adjacent non tumor tissue and that HMGB1 mRNA levels were higher in wild-type BRAF PTC tissues than in BRAF V600E PTC tissues (2-Delta Ct 0.31 +/- 0.25 vs. 0.16 +/- 0.12; P < 0.05). HMGB1 protein levels also differed in the same manner (wild-type BRAF PTC tissues 0.11 +/- 0.04 vs. BRAF V600E PTC tissues 0.03 +/- 0.03; P < 0.001). Although not detected in peripheral blood, low levels of HMGBI were significantly related to PTC cell lymph node metastasis and extra -glandular infiltration (P = 0.045 and P = 0.002). Experimental results at the cellular level were consistent with tissues and further verified the relationship of BRAF V600E and HMGB1. These findings demonstrate that the BRAF V600E mutation down-regulates levels of HMGB1, likely through activation of the mitogen-activated protein kinase (MAPK) signaling pathways. (C) 2017 Published by Elsevier Inc.
引用
收藏
页码:898 / 903
页数:6
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