| Literature DB >> 25755721 |
Jing Gao1, Zhengzhi Zou2, Jing Gao1, Haifang Zhang3, Zhicai Lin4, Yaya Zhang4, Xianyang Luo1, Changhua Liu4, Jingdun Xie5, Chengfu Cai1.
Abstract
HMGB3, an X-linked member of the high-mobility group (HMG) superfamily of HMG proteins, has been shown to affect numerous tumorigenic progression. However, the expression and the prognostic role of HMGB3 in esophageal squamous cell carcinoma (ESCC) remained unknown. In this study, we examined the HMGB3 expression in ESCC tissues and adjacent nontumorous tissues by qRT-PCR and immuohistochemistry. Statistical analyses were applied to test for prognostic and diagnostic associations. The mRNA levels of HMGB3 were found to be significantly higher in tumorous tissues than in the adjacent normal tissues. We found that the HMGB3 expression was higher in tumorous tissues than in the adjacent non-tumorous tissues by immunohistochemical analysis of paired tissue specimens (P < 0.001). Moreover, there was a significant correlation between HMGB3 expression and gender (P = 0.037), clinical stage (P = 0.038), T classification (P = 0.013) and N classification (P = 0.017). Patients with higher HMGB3 expression had shorter overall survival than those with lower HMGB3 expression. Multivariate Cox analysis indicated that HMGB3 expression is an independent prognostic factor for overall survival (HR = 0.591, 95% CI = 0.379-0.793, P = 0.039). In summary, these findings demonstrate that HMBG3 may be a potential molecular marker for predicting the prognosis of ESCC patients.Entities:
Keywords: HMGB3; biomarker; esophageal cancer; immunohistochemistry; prognosis; real-time PCR
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Year: 2015 PMID: 25755721 PMCID: PMC4348853
Source DB: PubMed Journal: Int J Clin Exp Pathol ISSN: 1936-2625