Expression of HIF-1[alpha] and HIF-2[alpha] correlates to biological and clinical significance in papillary thyroid carcinoma

Background The aim of this study was to detect the expression of hypoxia-inducible factor (HIF)-1[alpha] and HIF-2[alpha] in papillary thyroid carcinoma (PTC) compared with normal thyroid tissues. Methods The mRNA levels and protein levels of HIF-1[alpha] and HIF-2[alpha] were detected by real-time...

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Published inWorld journal of surgical oncology Vol. 14; no. 30
Main Authors Liu, Yan-Mei, Ying, Shen-Peng, Huang, Ying-Rui, Pan, Yin, Chen, Wei-Jun, Ni, Ling-Qin, Xu, Jin-Ye, Shen, Qin-Yan, Liang, Yong
Format Journal Article
LanguageEnglish
Published BioMed Central Ltd 04.02.2016
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Summary:Background The aim of this study was to detect the expression of hypoxia-inducible factor (HIF)-1[alpha] and HIF-2[alpha] in papillary thyroid carcinoma (PTC) compared with normal thyroid tissues. Methods The mRNA levels and protein levels of HIF-1[alpha] and HIF-2[alpha] were detected by real-time PCR and Western blot separately in 30 pairs of PTCs and normal thyroid cases. The protein levels were also detected by immunohistochemistry (IHC) using 92 samples of PTC group and 46 normal samples as control group for analyzing the biological and clinical significance of the expression of HIF-1[alpha]/HIF-2[alpha]. Results Real-time PCR results showed the mRNA level of HIF -1[alpha] and HIF-2[alpha] were significantly higher in PTC than normal group (P < 0.001). Also, significantly higher positive rates (73 %/65 %) of HIF-1[alpha] and HIF-2[alpha] were observed in PTC compared with the control group (27 %/35 %) by IHC (P 0.05), both of their expressions were correlated to lymph node metastasis (P < 0.05), capsular invasion (P < 0.05), and TNM stage (P < 0.05). Conclusions Overexpression of HIF-1[alpha] and HIF-2[alpha] are associated with the carcinogenesis of PTC, served as potential biomarkers of PTC. Keywords: HIF-1[alpha], HIF-2[alpha], RT-PCR, IHC, Western blot
ISSN:1477-7819
1477-7819
DOI:10.1186/s12957-016-0785-9