Tw. Beer et al., DETECTION OF THE MULTIDRUG-RESISTANCE MARKER P-GLYCOPROTEIN BY IMMUNOHISTOCHEMISTRY IN MALIGNANT LUNG-TUMORS, Thorax, 51(5), 1996, pp. 526-529
Background - The multidrug resistance marker P-glycoprotein (P-gp) was
studied immunohistochemically in 78 primary malignant lung rumours. P
-gp is a 170 kD transmembrane ATP dependent drug efflux pump which has
been shown to be important in the resistance of some tumours to chemo
therapy. Certain normal tissues express P-gp and tumours derived from
these tissues are often insensitive to cytotoxic agents, showing raise
d P-gp levels innately or following chemotherapy or radiotherapy. Meth
ods - Samples from 78 patients undergoing surgery for primary malignan
t lung tumours were snap frozen and stained immunohistochemically usin
g the monoclonal antibody C219 which reacts with a P-gp epitope. None
of the study group had received chemotherapy or radiotherapy before su
rgery was performed. Results - Twenty seven of the 78 lung tumours (34
.6%) showed immunohistochemically detectable levels of P-gp which vari
ed with tumour type; 17 of 54 squamous cell carcinomas (31.5%), seven
of 15 adenocarcinomas (46.7%), and neither of two small cell carcinoma
s showing positive staining. In six of seven cases normal respiratory
epithelium present showed the presence of P-gp. Conclusions - P-gp is
immunohistochemically detectable in frozen tissue from a proportion of
malignant lung rumours before exposure to radiotherapy or drugs assoc
iated with multidrug resistance. It may have a role in tumour resistan
ce to cytotoxic drugs, but further clinical studies will be required t
o evaluate any correlation between P-gp levels and response to treatme
nt.