|
Resolution: standard / high Figure 7.
Immunohistochemical staining for HRGβ1 in primary breast cancer specimens. (a) Examples of high and low HRGβ1 expression. Scale bars = 20 μm. (b) Box-plots illustrating cytoplasmic HRGβ1 immunohistochemistry assessed by H-score
analysis in membrane (mem) epidermal growth factor receptor (EGFR)-negative, erbB2-negative
and erbB3-negative primary breast cancer versus membrane EGFR-positive, erbB2-positive
and erbB3-positive primary breast cancer. A significant positive correlation between
cytoplasmic HRGβ1 expression and membrane erbB receptor positivity was only seen with
EGFR (Mann–Whitney U test, P = 0.04). (c) Box-plots illustrating cytoplasmic HRGβ1 immunohistochemistry assessed by H-score
analysis in membrane (mem) phosphorylated erbB2-negative versus membrane phosphorylated
erbB2-positive primary breast cancer and in nuclear (nuc) phosphorylated ERK1/2-negative
versus nuclear phosphorylated ERK1/2-positive primary breast cancer (Mann–Whitney
U test, P = 0.006 and P = 0.017, respectively), and scatter plot illustrating the significant positive correlation
between expression levels of nuclear phosphorylated AKT and cytoplasmic HRGβ1 in the
same samples (Spearman rank test, P = 0.044).
Hutcheson et al. Breast Cancer Research 2007 9:R50 doi:10.1186/bcr1754 |