作者: Xiaolei Guan , Ping Wang , Jingwei Chi , Shihua Zhao , Fei Wang
DOI: 10.1016/J.BBRC.2017.03.117
关键词:
摘要: A poor papillary thyroid cancer (PTC) prognosis is strongly associated with the BRAF V600E mutation. During tumor progression, levels of high mobility group box 1 (HMGB1) protein are often dysregulated. Results herein demonstrate that HMGB1 differ between and adjacent non-tumor tissue mRNA were higher in wild-type PTC tissues than (2-△Ct 0.31 ± 0.25 vs. 0.16 ± 0.12; P < 0.05). also differed same manner (wild-type 0.11 ± 0.04 0.03 ± 0.03; P < 0.001). Although not detected peripheral blood, low significantly related to cell lymph node metastasis extra-glandular infiltration (P = 0.045 P = 0.002). Experimental results at cellular level consistent further verified relationship HMGB1. These findings mutation down-regulates HMGB1, likely through activation mitogen-activated kinase (MAPK) signaling pathways.