Glyceraldehyde-3-phosphate dehydrogenase gene expression in human breast cancer

Abstract

Glyceraldehyde-3-phosphate dehydrogenase ( GAPDH) has been widely used as a control RNA in Northern blotting and in reverse transcriptase–polymerase chain reaction (RT–PCR) analyses. We investigated the expression of GAPDH in a large series of primary breast cancers and in MCF7 human mammary epithelial breast cancer cells treated with oestradiol. The expression of GAPDH was quantified by a real-time one-step RT–PCR assay, based upon the 5′ nuclease activity of Taq polymerase using an Abi Prism 7700 Sequence Detector System (Perkin Elmer, France). Using the Spearman test, GAPDH expression was found to correlate inversely with the age of the patients at diagnosis ( P=0.003; r=−0.147), oestradiol receptors (ER) ( P<0.0001; r=−0.327) and progesterone receptors (PgR) ( P<0.0001; r=−0.206). A positive correlation was observed between GAPDH expression and the histo-prognostic grading (HPG) ( P<0.0001; r=0.344). Moreover, the overall survival (OS) and the relapse-free survival (RFS) were significantly reduced in patients whose tumours showed an enhanced level of GAPDH expression (OS, P=0.046; RFS, P=0.021). Multivariate analyses demonstrated that GAPDH was not an independent prognostic factor. Finally, in MCF7 cells treated with oestradiol, a statistically significant dose-dependent increase in GAPDH expression was observed. These results show that GAPDH expression is associated with breast cancer cell proliferation and with the aggressiveness of tumours. The present study demonstrates that, in cancer, the use of GAPDH gene expression should not be used as a control RNA.