Human tumor xenografts in nude mice are widely utilized model system for th
e transplantation of human surgical specimens and human established cell li
nes. Gene expression studies are often carried out in these model systems.
With an increasing use of PCR based analyses, the extreme sensitivity of th
is technique poses a serious challenge with regards to the extent of contam
inating host mouse cells in the human tumor xenografts. These xenografts ar
e never fr ee of host cell contamination. We detected mouse estrogen recept
or expression in several human tumor xenografts using RT-PCR demonstrating
that precaution is necessary when utilizing PCR based analyses in human tum
or xenografts. A cytologically based methodology which distinguishes human
versus mouse cells will be more suitable for ER expression studies using hu
man xenograft models Both (1) in situ hybridization using human probe and (
2) immunocytochemistry using a monoclonal antibody directed against human c
ytokeratin have been used successfully to distinguish human cells versus ho
st mouse cells in human xenografts in nude mice. Immunostaining of ER can t
hen be utilized to determine the expression pattern of ER in the transplant
ed human cells.