P. Engblom et al., PACLITAXEL AND CISPLATIN SENSITIVITY OF OVARIAN-CARCINOMA CELL-LINES TESTED WITH THE 96-WELL PLATE CLONOGENIC-ASSAY, Anticancer research, 16(4A), 1996, pp. 1743-1747
Platinum based chemotherapy is the cornerstone of treatment in advance
d ovarian carcinoma. Paclitaxel, an unique antimicrotubule agent has s
hown significant clinical activity in cisplatin-resistant tumours, ind
icating a lack of cross-resistance. to compare the in vitro sensitivit
y of ovarian carcinoma to cisplatin and paclitaxel, we tested 7 ovaria
n carcinoma cell lines with the 96-well plate clonogenic assay. Chemos
ensitivity was expressed as the IC50 values for paclitacel were 0.4-3.
4 nM, showing an 8.5-fold difference between various cell lines. The I
C50 values for cisplatin were 0.1-0.45 ug ml(-1) showing only a 4.5-fo
ld difference. This variance is clearly smaller than the 25-fold diffe
rence observed with the same method in endometrial carcinoma cell line
s (Rantanen et al, Br J Cancer 69: 482-86, 1994). In accordance with c
linical findings, no cross-resistance or correlation between sensitivi
ty to paclitaxel and cisplatin could be demonstrated.