Hypoxia inducible factor 1α gene (HIF-1α) splice variants: potential prognostic biomarkers in breast cancer

被引:43
作者
Dales, Jean-Philippe [1 ,2 ]
Beaufils, Nathalie
Silvy, Monique [3 ]
Picard, Christophe [3 ]
Pauly, Vanessa [4 ]
Pradel, Vincent [4 ]
Formisano-Treziny, Christine [1 ]
Bonnier, Pascal [5 ]
Giusiano, Sophie [2 ]
Charpin, Colette [2 ]
Gabert, Jean [1 ]
机构
[1] Plateforme Transcriptome, CRO2, Marseille, France
[2] Hop Nord Marseille, Dept Pathol, Marseille, France
[3] Etablissement Francais Sang Alpes Mediterranee, Marseille, France
[4] Hop St Marguerite, Dept Med Informat, Marseille, France
[5] Univ Aix Marseille 2, Hop Concept, AP HP, Dept Gynaecol Oncol, Marseille, France
来源
BMC MEDICINE | 2010年 / 8卷
关键词
RECEPTOR IMMUNOCYTOCHEMICAL ASSAY; DOMINANT-NEGATIVE ISOFORM; NUCLEAR-TRANSLOCATOR; O-2; TENSION; DNA-BINDING; FACTOR-LOT; FACTOR-1-ALPHA; EXPRESSION; TRANSACTIVATION; OVEREXPRESSION;
D O I
10.1186/1741-7015-8-44
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Hypoxia-inducible factor 1 (HIF-1) is a master transcriptional regulator of genes regulating oxygen homeostasis. The HIF-1 protein is composed of two HIF-1 alpha and HIF-1 beta/aryl hydrocarbon receptor nuclear translocator (ARNT) subunits. The prognostic relevance of HIF-1 alpha protein overexpression has been shown in breast cancer. The impact of HIF-1 alpha alternative splice variant expression on breast cancer prognosis in terms of metastasis risk is not well known. Methods: Using real-time quantitative reverse transcription PCR assays, we measured mRNA concentrations of total HIF-1 alpha and 4 variants in breast tissue specimens in a series of 29 normal tissues or benign lesions (normal/benign) and 53 primary carcinomas. In breast cancers HIF-1 alpha splice variant levels were compared to clinicopathological parameters including tumour microvessel density and metastasis-free survival. Results: HIF-1 alpha isoforms containing a three base pairs TAG insertion between exon 1 and exon 2 (designated HIF-1 alpha(TAG)) and HIF-1 alpha(736) mRNAs were found expressed at higher levels in oestrogen receptor (OR)-negative carcinomas compared to normal/benign tissues (P = 0.009 and P = 0.004 respectively). In breast carcinoma specimens, lymph node status was significantly associated with HIF-1 alpha(TAG) mRNA levels (P = 0.037). Significant statistical association was found between tumour grade and HIF-1 alpha(TAG) (P = 0.048), and total HIF-1 alpha (P = 0.048) mRNA levels. HIF-1 alpha(TAG) mRNA levels were also inversely correlated with both oestrogen and progesterone receptor status (P = 0.005 and P = 0.033 respectively). Univariate analysis showed that high HIF-1 alpha(TAG) mRNA levels correlated with shortened metastasis free survival (P = 0.01). Conclusions: Our results show for the first time that mRNA expression of a HIF-1 alpha(TAG) splice variant reflects a stage of breast cancer progression and is associated with a worse prognosis. See commentary: http://www.biomedcentral.com/1741-7015/8/45
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页数:11
相关论文
共 40 条
[1]  
Bièche I, 1999, CANCER RES, V59, P2759
[2]   HISTOLOGICAL GRADING AND PROGNOSIS IN BREAST CANCER - A STUDY OF 1409 CASES OF WHICH 359 HAVE BEEN FOLLOWED FOR 15 YEARS [J].
BLOOM, HJG ;
RICHARDSON, WW .
BRITISH JOURNAL OF CANCER, 1957, 11 (03) :359-&
[3]   aHIF but not HIF-1α transcript is a poor prognostic marker in human breast cancer [J].
Cayre, A ;
Rossignol, F ;
Clottes, E ;
Penault-Llorca, F .
BREAST CANCER RESEARCH, 2003, 5 (06) :R223-R230
[4]  
CHARPIN C, 1988, AM J PATHOL, V132, P199
[5]  
CHARPIN C, 1988, CANCER RES, V48, P1578
[6]  
Chun YS, 2003, CANCER RES, V63, P8700
[7]   A dominant-negative isoform lacking exons 11 and 12 of the human hypoxia-inducible factor-1α gene [J].
Chun, YS ;
Choi, E ;
Kim, TY ;
Kim, MS ;
Park, JW .
BIOCHEMICAL JOURNAL, 2002, 362 (01) :71-79
[8]  
Chun YS, 2001, J CELL SCI, V114, P4051
[9]   Overexpression of hypoxia-inducible factor HIF-1α predicts early relapse in breast cancer:: Retrospective study in a series of 745 patients [J].
Dales, JP ;
Garcia, S ;
Meunier-Carpentier, S ;
Andrac-Meyer, L ;
Haddad, O ;
Lavaut, MN ;
Allasia, C ;
Bonnier, P ;
Charpin, C .
INTERNATIONAL JOURNAL OF CANCER, 2005, 116 (05) :734-739
[10]  
Dales JP, 2004, INT J ONCOL, V24, P1197