Abstract

BackgroundHypoxia-inducible factor 1 (HIF-1) is a master transcriptional regulator of genes regulating oxygen homeostasis. The HIF-1 protein is composed of two HIF-1α and HIF-1β/aryl hydrocarbon receptor nuclear translocator (ARNT) subunits. The prognostic relevance of HIF-1α protein overexpression has been shown in breast cancer. The impact of HIF-1α alternative splice variant expression on breast cancer prognosis in terms of metastasis risk is not well known.MethodsUsing real-time quantitative reverse transcription PCR assays, we measured mRNA concentrations of total HIF-1α 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-1α splice variant levels were compared to clinicopathological parameters including tumour microvessel density and metastasis-free survival.ResultsHIF-1α isoforms containing a three base pairs TAG insertion between exon 1 and exon 2 (designated HIF-1αTAG) and HIF-1α736 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-1αTAG mRNA levels (P = 0.037). Significant statistical association was found between tumour grade and HIF-1αTAG (P = 0.048), and total HIF-1α (P = 0.048) mRNA levels. HIF-1αTAG 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-1αTAG mRNA levels correlated with shortened metastasis free survival (P = 0.01).ConclusionsOur results show for the first time that mRNA expression of a HIF-1αTAG 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

Highlights

  • Hypoxia-inducible factor 1 (HIF-1) is a master transcriptional regulator of genes regulating oxygen homeostasis

  • We investigated the prognostic value of HIF-1a transcript expression levels in breast cancer and found a significant relationship between either clinicopathological characteristics or patient metastasis-free survival

  • The second and most striking observation was that HIF-1aTAG mRNA levels were indicative of shorter metastasis-free survival, and that this correlated with lymph node status

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Summary

Introduction

Hypoxia-inducible factor 1 (HIF-1) is a master transcriptional regulator of genes regulating oxygen homeostasis. Hypoxia-inducible factor 1 (HIF-1) is a ubiquitously expressed master transcriptional regulator of many genes regulating mammalian oxygen homeostasis [1,2]. HIF-1 is a heterodimeric protein composed of two HIF-1a and HIF-1b/aryl hydrocarbon receptor nuclear translocator (ARNT) subunits [5]. HIF-1a protein is overexpressed because of intratumoural hypoxia and genetic alterations affecting key oncogenes and tumour suppressor genes [8,9]. This overexpression correlates with tumour angiogenesis, treatment failure and patient mortality [3]

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