The aim of the study was to determine whether electrochemotherapy with cisp
latin could be implemented in treatment of cisplatin-resistant solid tumour
s. For this purpose, we used cisplatin-sensitive TBL.C12 cells and their ci
splatin-resistant subclone TBL.C12 Pt, which can be grown as in vitro cell
cultures and as solid subcutaneous tumours in C57B1/6 mice. Cytotoxicity of
cisplatin alone and combined with electroporation was determined by colony
forming assay. Treatment effects of electrochemotherapy in vivo were asses
sed by tumour growth delay and tumour curability. Platinum content in the c
ells and tumours was determined by atomic absorption spectroscopy. In vitro
, TBL.C12 Pt cells were equally sensitive to electrochemotherapy us their c
isplatin-sensitive: counterparts. In vivo, electrochemotherapy was effectiv
e on both tumour types, resulting in a prolonged tumour growth delay and tu
mour cures. However, electrochemotherapy was more effective on parental tha
n cisplatin-resistant tumours, in which platinum content was significantly
lower compared with parental tumours. In conclusion, electrochemotherapy is
an effective treatment of cisplatin-resistant solid tumours and may prove
useful in clinical chemotherapy for the treatment of tumours with intrinsic
or acquired resistance to cisplatin. (C) 2001 Elsevier Science Ltd. All ri
ghts reserved.