BACKGROUND: The multidrug resistance marker P-glycoprotein (P-gp) was studied immunohistochemically in 78 primary malignant lung tumours. 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 chemotherapy. Certain normal tissues express P-gp and tumours derived from these tissues are often insensitive to cytotoxic agents, showing raised P-gp levels innately or following chemotherapy or radiotherapy. METHODS: Samples from 78 patients undergoing surgery for primary malignant lung tumours were snap frozen and stained immunohistochemically using the monoclonal antibody C219 which reacts with a P-gp epitope. None of the study group had received chemotherapy or radiotherapy before surgery was performed. RESULTS: Twenty seven of the 78 lung tumours (34.6%) showed immunohistochemically detectable levels of P-gp which varied with tumour type; 17 of 54 squamous cell carcinomas (31.5%), seven of 15 adenocarcinomas (46.7%), and neither of two small cell carcinomas 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 tumours before exposure to radiotherapy or drugs associated with multidrug resistance. It may have a role in tumour resistance to cytotoxic drugs, but further clinical studies will be required to evaluate any correlation between P-gp levels and response to treatment.
BACKGROUND: The multidrug resistance marker P-glycoprotein (P-gp) was studied immunohistochemically in 78 primary malignant lung tumours. 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 chemotherapy. Certain normal tissues express P-gp and tumours derived from these tissues are often insensitive to cytotoxic agents, showing raised P-gp levels innately or following chemotherapy or radiotherapy. METHODS: Samples from 78 patients undergoing surgery for primary malignant lung tumours were snap frozen and stained immunohistochemically using the monoclonal antibody C219 which reacts with a P-gp epitope. None of the study group had received chemotherapy or radiotherapy before surgery was performed. RESULTS: Twenty seven of the 78 lung tumours (34.6%) showed immunohistochemically detectable levels of P-gp which varied with tumour type; 17 of 54 squamous cell carcinomas (31.5%), seven of 15 adenocarcinomas (46.7%), and neither of two small cell carcinomas 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 tumours before exposure to radiotherapy or drugs associated with multidrug resistance. It may have a role in tumour resistance to cytotoxic drugs, but further clinical studies will be required to evaluate any correlation between P-gp levels and response to treatment.
Authors: S A Pileri; E Sabattini; B Falini; P L Tazzari; F Gherlinzoni; M G Michieli; D Damiani; L Zucchini; M Gobbi; T Tsuruo Journal: Histopathology Date: 1991-08 Impact factor: 5.087
Authors: Y Segawa; T Ohnoshi; S Hiraki; H Ueoka; K Kiura; H Kamei; M Tabata; T Shibayama; K Miyatake; K Genba Journal: Acta Med Okayama Date: 1993-06 Impact factor: 0.892
Authors: R Milroy; J A Plumb; P Batstone; A Maclay; G C Wishart; F G Hay; W Candlish; R Adamson; M Z Khan; S Banham Journal: Anticancer Res Date: 1992 Jan-Feb Impact factor: 2.480
Authors: D Schlaifer; G Laurent; S Chittal; T Tsuruo; S Soues; C Muller; J Y Charcosset; C Alard; P Brousset; C Mazerrolles Journal: Br J Cancer Date: 1990-08 Impact factor: 7.640
Authors: Margaretha van der Deen; Elisabeth G E de Vries; Wim Timens; Rik J Scheper; Hetty Timmer-Bosscha; Dirkje S Postma Journal: Respir Res Date: 2005-06-20