Analysis of HAX-1 gene expression in esophageal squamous cell carcinoma.
Analysis of HAX-1 gene expression in esophageal squamous cell carcinoma.
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DOI:
10.1186/1746-1596-8-47
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发表时间:
2013-03-25
影响因子:
2.6
通讯作者:
Zhao G
中科院分区:
文献类型:
--
作者:
Li M;Tang Y;Zang W;Xuan X;Wang N;Ma Y;Wang Y;Dong Z;Zhao G
To explore the expression of HAX-1 mRNA and protein in esophageal squamous cell carcinoma (ESCC) and its relation with the prognosis of patients with ESCC. The expression of HAX-1 mRNA and protein were detected with quantitative real-time RT-PCR and immunohistochemical method in 112 ESCC samples and 112 corresponding non-neoplastic samples. Survival curves were made with follow-up data. The relations of the prognosis with clinical and pathological characteristics were analyzed. The expression level of HAX-1 mRNA and the strong positive rate of HAX-1 protein were significantly higher in ESCC samples (0.527 ± 0.060 and 45.54%) than that in non-neoplastic samples (0.121 ± 0.017 and 0.00%), and in ESCC samples with lymph node metastasis (0.554 ± 0.054 and 71.11%) than that in ESCC samples without lymph node metastasis (0.509 ± 0.058 and 28.36%) (all P < 0.01). HAX-1 mRNA expression level was a risk factor of lymph node metastasis in patients with ESCC (P = 0.000). There were significant differences in survival curves between lymph node metastatic group and non-metastatic group (P = 0.000), and among groups of HAX-1 protein expression +, ++and +++(,P = 0.000); but no statistical significance between male patients and female patients (P = 0.119), and between ≥60 years old patients and <60 years old patients (P = 0.705). The level of HAX-1 mRNA (P = 0.000) and protein (P = 0.005) were risk factors of survival, but lymph node metastasis (P = 0.477) was not. There is HAX-1 over-expression in ESCC tissue and HAX-1 mRNA level is a risk factor of lymph node metastasis. The level of HAX-1 mRNA and protein were risk factors of survival in patients with ESCC. HAX-1 may be a novel therapeutic target for ESCC treatment. The virtual slide(s) for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/5130393079296037
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影响因子:
3.8
作者:
Trebinska A;Rembiszewska A;Ciosek K;Ptaszynski K;Rowinski S;Kupryjanczyk J;Siedlecki JA;Grzybowska EA
通讯作者:
Grzybowska EA
影响因子:
4.8
作者:
Rhodes, DR;Yu, JJ;Chinnaiyan, AM
通讯作者:
Chinnaiyan, AM
影响因子:
3.1
作者:
Sun, Sa-jia;Feng, Long;Dong, Zi-ming
通讯作者:
Dong, Zi-ming
影响因子:
11.1
作者:
Carlsson, G.;van't Hooft, I.;Henter, J-I
通讯作者:
Henter, J-I
影响因子:
5.4
作者:
Banerjee, Arup;Saito, Kousuke;Ray, Ranjit
通讯作者:
Ray, Ranjit