We hypothesize that interleukin-1 alpha, beta, and receptor antagonist (IL-
1 alpha, IL-1 beta, and IL-1ra, respectively) are present and tumor cell as
sociated in human breast cancer (HBC). We believe the levels of these cytok
ines in breast tumor homogenates relate to other known prognosticators of p
atient survival (i.e., estrogen receptor [ER] status). Our results demonstr
ated that, immunohistochemically, tumor cells express IL-1 alpha, IL-1 beta
, and IL-1ra in most specimens tested. In breast tissue homogenates, IL-1 a
lpha levels correlated inversely with ER levels (p < 0.06), whereas IL-1ra
levels correlated directly with both ER levels (p < 0.009) and IL-1 beta le
vels (p < 0.06). When analyzing cytokine levels for the ER (-) versus ER () patient groups, we found that in many instances these groups showed a dif
ferent cytokine profile. These studies suggest that the IL-1 family of cyto
kines may be important in regulating protumorigenic activities within the H
BC tumor microenvironment.