PMID- 3229319 OWN - NLM STAT- MEDLINE DCOM- 19890418 LR - 20071114 IS - 0378-6501 (Print) IS - 0378-6501 (Linking) VI - 14 IP - 9 DP - 1988 TI - A new antitumour agent, batracylin, selected by a preclinical solid tumour model. PG - 571-4 AB - The antitumour efficacy of batracylin was investigated in vivo against murine tumours. The drug displayed an original spectrum of activity. It was totally inactive against L1210 leukaemia and B16 melanoma, while it was marginally active against ascitic P388 leukaemia. However, the tumour growth of the subcutaneously (s.c.) implanted colon 38 adenocarcinoma (Co 38) was completely inhibited in 80-90% of the mice. Therapeutic efficacy was retained upon oral administration and the drug was able to induce tumour regression in the advanced Co 38 disease. These data justify the selection of batracylin for toxicological studies and possible clinical investigations. FAU - Atassi, G AU - Atassi G AD - Jules Bordet Institute, Free University of Brussels, Belgium. FAU - Dumont, P AU - Dumont P FAU - Kabbe, H J AU - Kabbe HJ FAU - Yoder, O AU - Yoder O LA - eng GR - N01-CM-57645/CM/NCI NIH HHS/United States PT - Journal Article PT - Research Support, Non-U.S. Gov't PT - Research Support, U.S. Gov't, P.H.S. PL - Switzerland TA - Drugs Exp Clin Res JT - Drugs under experimental and clinical research JID - 7802135 RN - 0 (Antineoplastic Agents) RN - 0 (Quinazolines) RN - 67199-66-0 (batracylin) SB - IM MH - Adenocarcinoma/*drug therapy MH - Animals MH - Antineoplastic Agents/*therapeutic use MH - Colonic Neoplasms/*drug therapy MH - *Drug Screening Assays, Antitumor MH - Leukemia L1210/drug therapy MH - Leukemia P388/drug therapy MH - Melanoma, Experimental/drug therapy MH - Mice MH - Quinazolines/*therapeutic use EDAT- 1988/01/01 00:00 MHDA- 1988/01/01 00:01 CRDT- 1988/01/01 00:00 PHST- 1988/01/01 00:00 [pubmed] PHST- 1988/01/01 00:01 [medline] PHST- 1988/01/01 00:00 [entrez] PST - ppublish SO - Drugs Exp Clin Res. 1988;14(9):571-4.