TY - JOUR
T1 - Unique features of the mode of action of ET-743
AU - D'Incalci, Maurizio
AU - Erba, Eugenio
AU - Damia, Giovanna
AU - Galliera, Emanuela
AU - Carrassa, Laura
AU - Marchini, Sergio
AU - Mantovani, Roberto
AU - Tognon, Gianluca
AU - Fruscio, Robert
AU - Jimeno, José
AU - Faircloth, Glynn T.
PY - 2002
Y1 - 2002
N2 - This paper describes the current knowledge of the primary mode of action of a natural product, ecteinascidin 743 (ET-743), derived from the marine tunicate Ecteinascidia turbinata. ET-743 was initially selected for preclinical development because of its potent antitumor activity observed against several human solid tumor types. In vitro, the drug is cytotoxic in the nanomolar range, and in the case of some very sensitive cell lines, in the picomolar range. The large potency differences observed among several solid tumor types indicate that this compound possesses some tumor selectivity, but the molecular basis of these differential effects remains to be elucidated. The present studies were undertaken to evaluate the mechanism of action of ET-743 in this context. The available information on ET-743 binding to DNA and its effects on transcriptional regulation point to a unique behavior of this drug, as it independently affects specific gene transcription in a promoter-dependent way. In addition, ET-743 shows a peculiar pattern of selectivity in cells with different defects in their DNA-repair pathways. These results highlight a unique property of ET-743, possibly explaining why it possesses antitumor activity against tumors that are refractory to standard anticancer drugs, all of which certainly act by mechanisms that are different from that of ET-743.
AB - This paper describes the current knowledge of the primary mode of action of a natural product, ecteinascidin 743 (ET-743), derived from the marine tunicate Ecteinascidia turbinata. ET-743 was initially selected for preclinical development because of its potent antitumor activity observed against several human solid tumor types. In vitro, the drug is cytotoxic in the nanomolar range, and in the case of some very sensitive cell lines, in the picomolar range. The large potency differences observed among several solid tumor types indicate that this compound possesses some tumor selectivity, but the molecular basis of these differential effects remains to be elucidated. The present studies were undertaken to evaluate the mechanism of action of ET-743 in this context. The available information on ET-743 binding to DNA and its effects on transcriptional regulation point to a unique behavior of this drug, as it independently affects specific gene transcription in a promoter-dependent way. In addition, ET-743 shows a peculiar pattern of selectivity in cells with different defects in their DNA-repair pathways. These results highlight a unique property of ET-743, possibly explaining why it possesses antitumor activity against tumors that are refractory to standard anticancer drugs, all of which certainly act by mechanisms that are different from that of ET-743.
KW - Anticancer drug
KW - ET-743
KW - Marine compound
KW - Natural product
UR - http://www.scopus.com/inward/record.url?scp=18444404938&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=18444404938&partnerID=8YFLogxK
U2 - 10.1634/theoncologist.7-3-210
DO - 10.1634/theoncologist.7-3-210
M3 - Article
C2 - 12065793
AN - SCOPUS:18444404938
SN - 1083-7159
VL - 7
SP - 210
EP - 216
JO - Oncologist
JF - Oncologist
IS - 3
ER -