Protein kinase Cδ expression in breast cancer as measured by real-time PCR, western blotting and ELISA
The protein kinase C (PKC) family of genes encode serine/threonine kinases that regulate proliferation, apoptosis, cell survival and migration. Multiple isoforms of PKC have been described, one of which is PKCδ. Currently, it is unclear whether PKCδ is involved in promoting or inhibiting cancer formation/progression. The aim of this study was therefore to investigate the expression of PKCδ in human breast cancer and relate its levels to multiple parameters of tumour progression. Protein kinase Cδ expression at the mRNA level was measured using real-time PCR (n=208) and at protein level by both immunoblotting (n=94) and ELISA (n=98). Following immunoblotting, two proteins were identified, migrating with molecular masses of 78 and 160 kDa. The 78 kDa protein is likely to be the mature form of PKCδ but the identity of the 160 kDa form is unknown. Levels of both these proteins correlated weakly but significantly with PKCδ concentrations determined by ELISA (for the 78 kDa form, r=0.444, P<0.005, n=91 and for the 160 kDa form, r=0.237, P=0.023, n=91) and with PKCδ mRNA levels (for the 78 kDa form, r=0.351, P=0.001, n=94 and for the 160 kDa form, r=0.216, P=0.037, n=94). Protein kinase Cδ mRNA expression was significantly higher in oestrogen receptor (ER)-positive compared with ER-negative tumours (P=0.007, Mann-Whitney U-test). Increasing concentrations of PKCδ mRNA were associated with reduced overall patient survival (P=0.004). Our results are consistent with a role for PKCδ in breast cancer progression.
|Keywords||Breast cancer, Protein kinase Cδ|
|Persistent URL||dx.doi.org/10.1038/sj.bjc.6604728, hdl.handle.net/1765/29150|
|Note||Free full text at PubMed|
McKiernan, E, O'Brien, K, Grebenchtchikov, N, Geurts-Moespot, A, Sieuwerts, A.M, Martens, J.W.M, … Duffy, M.J. (2008). Protein kinase Cδ expression in breast cancer as measured by real-time PCR, western blotting and ELISA. British Journal of Cancer, 99(10), 1644–1650. doi:10.1038/sj.bjc.6604728