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Splice variant HE4-V3 expression is associated with favorable prognosis in pulmonary adenocarcinoma.

Authors :
Tokuishi K
Yamashita S
Ohbo K
Kawahara K
Source :
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine [Tumour Biol] 2012 Feb; Vol. 33 (1), pp. 103-9. Date of Electronic Publication: 2011 Oct 21.
Publication Year :
2012

Abstract

The human epididymis 4 (HE4) gene product, also known as whey-acidic-protein four-disulfide core domain protein 2, was identified as the transcript expressed in the epididymis and respiratory tract. HE4 is also expressed in lung adenocarcinoma. We investigated mRNA expressions of full-length HE4 and splice variants in lung adenocarcinoma, and the clinical impact of these genes was evaluated. One hundred and fifty-two patients with pulmonary adenocarcinoma underwent surgery in our institute from 2000 to 2008. We employed immunohistochemical analysis to determine the expression of HE4 and molecular analysis to evaluate full-length HE4 or splice variant gene expression in pulmonary adenocarcinoma. All of the 152 cases were full-length HE4 mRNA-positive; 88 of the 152 (57.9%) were HE4-V1-positive, and 140 of the 152 (92.1%) were HE4-V3-positive. Regarding the relationship between the clinicopathological characteristics of patients and these gene expressions, the histological subtype, tumor size, and vascular invasion were significantly associated with HE4-V3 expression. HE4-V3 expression was also closely correlated with the prognosis. The 5-year disease-free survival in the HE4-V3 high expression group showed a significantly favorable prognosis compared with the low expression group (p = 0.02). The 5-year overall survival rate in the HE4-V3 high expression group was significantly higher than in the HE4-V3 low expression group (p = 0.028). These data showed that high-level HE4-V3 expression is associated with a favorable prognosis in lung adenocarcinoma. Further investigation of HE4 splice variants may offer a new insight into this possibility.

Details

Language :
English
ISSN :
1423-0380
Volume :
33
Issue :
1
Database :
MEDLINE
Journal :
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine
Publication Type :
Academic Journal
Accession number :
22015929
Full Text :
https://doi.org/10.1007/s13277-011-0252-8