Expression of p53 isoforms in renal cell carcinoma

Background Several isoforms of p53 have been reported, which may have varying functions and expressions. This study aimed to analyze the expression patterns of p53 isoforms in renal cell carcinoma （RCC） at the mRNA and protein levels and their associations with clinical and pathologic factors to explore the mechanism of p53 isoforms＇ activity in RCC. Methods The specimens of tumours （T） and clinically normal tissues （N） adjacent to them were collected from 41 patients with RCC. mRNA expression levels of p53 isoforms were detected using RT-PCR followed by nested PCR. Protein expression levels were detected using immunohistochemisty and Western blotting with the anti-p53 antibodies DO-1 and DO-12. The data were analyzed with clinicopathological features by X^2 test or Fisher＇s exact test. Results p53 mRNA was expressed in all tumours and matched clinically normal tissue adjacent to the tumour. All six isoforms could be detected in tumour and normal tissues, with the exception of the △133p53β isoform, which was not detected in the normal tissue. Of the six isoforms, p53β mRNA was significantly overexpressed in tumour samples （P 〈0.001）, and correlated with tumour stage. Nested PCR results consistently indicated the presence of p53γ （19T/22N）, △133p53 （33T/26N）, △133p53β （2T/0N）, and △133p53γ （13T/9N）. Immunohistochemical analysis showed that p53 was expressed only in tumour tissues and correlated with tumour stage and grade. The results of Western blotting analysis were consistent with these findings. Conclusions Although all six isoforms are present in RCC, their function in tumour development or progression might be different. Our findings suggest that p53β might play an important role in the formation of RCC and it might be used as a new predictor and therapeutic target for RCC.