TY - JOUR
T1 - Synergistic inhibition of growth and induction of apoptosis by 8- chloro-cAMP and paclitaxel or cisplatin in human cancer cells
AU - Tortora, Giampaolo
AU - Di Isernia, Giuditta
AU - Sandomenico, Claudia
AU - Bianco, Roberto
AU - Pomatico, Grazia
AU - Pepe, Stefano
AU - Bianco, A. Raffaele
AU - Ciardiello, Fortunato
PY - 1997/11/15
Y1 - 1997/11/15
N2 - 8-Chloro-cAMP (8-Cl-cAMP) is novel agent that is able to inhibit the growth of a wide variety of cancer cell types in vitro and in vivo and, at doses devoid of toxicity, to achieve plasma concentrations in cancer patients in a range effective for cancer cell growth inhibition. In this study, we have demonstrated that 8-Cl-cAMP, at a dose causing mild or no growth inhibition, synergistically increased the growth-inhibitory effect of paclitaxel or cisplatin in a wide series of cell lines including human breast, lung, ovary, colon, and head carcinomas and melanoma. A similar effect was also observed with another taxane, docetaxel, and with the platinum-derivative carboplatin, 8-Cl-cAMP also markedly enhanced apoptotic cell death induced by each cytotoxic drug. A cooperative antitumor effect was also observed in vivo, because treatment with paclitaxel followed by 8-Cl- cAMP markedly inhibited the growth of GEO human colon cancer xenografts as compared to paclitaxel alone without signs of toxicity. These data demonstrate that 8-Cl-cAMP synergistically increases the antiproliferative activity of taxanes and platinum-derived compounds and provide a rationale to use 8-Cl-cAMP in combination with taxanes and platinum derived compounds.
AB - 8-Chloro-cAMP (8-Cl-cAMP) is novel agent that is able to inhibit the growth of a wide variety of cancer cell types in vitro and in vivo and, at doses devoid of toxicity, to achieve plasma concentrations in cancer patients in a range effective for cancer cell growth inhibition. In this study, we have demonstrated that 8-Cl-cAMP, at a dose causing mild or no growth inhibition, synergistically increased the growth-inhibitory effect of paclitaxel or cisplatin in a wide series of cell lines including human breast, lung, ovary, colon, and head carcinomas and melanoma. A similar effect was also observed with another taxane, docetaxel, and with the platinum-derivative carboplatin, 8-Cl-cAMP also markedly enhanced apoptotic cell death induced by each cytotoxic drug. A cooperative antitumor effect was also observed in vivo, because treatment with paclitaxel followed by 8-Cl- cAMP markedly inhibited the growth of GEO human colon cancer xenografts as compared to paclitaxel alone without signs of toxicity. These data demonstrate that 8-Cl-cAMP synergistically increases the antiproliferative activity of taxanes and platinum-derived compounds and provide a rationale to use 8-Cl-cAMP in combination with taxanes and platinum derived compounds.
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M3 - Article
C2 - 9371510
AN - SCOPUS:0030722087
SN - 0008-5472
VL - 57
SP - 5107
EP - 5111
JO - Journal of Cancer Research
JF - Journal of Cancer Research
IS - 22
ER -