Antitumor activity of quinocarmycin against carcinoma of the lung in human tumor clonogenic assay.

Abstract

Quinocarmycin monocitrate is a novel antitumor antibiotic isolated from Streptomyces melanovinaceus. We have utilized a human tumor clonogenic assay to test the antitumor activity of this drug against carcinoma of the lung and to compare its activity with those of mitomycin C or cisplatin, which are components of the clinically effective regimens in therapy for this disease. The overall in vitro response rate (defined as less than 50% survival of tumor colony forming units) for quinocarmycin at 0.1 and 1.0 microgram/ml continuous exposure was 42% and 72%, respectively, which was superior to that of other drugs. Quinocarmycin and other antitumor drugs do not have identical spectra of antitumor activities in vitro, suggesting that this compound with good in vitro activity should be further developed for clinical trials.

• Authors: C D Chiang, F Kanzawa, Y Matsushima, H Nakano, K Nakagawa, H Takahashi, M Terada, S Morinaga, R Tsuchiya, Y Sasaki
• Journal: Journal of pharmacobio-dynamics (J Pharmacobiodyn) Vol. 10 Issue 9 Pg. 431-5 (Sep 1987) ISSN: 0386-846X [Print] Japan
• PMID: 3437383 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antibiotics, Antineoplastic
• Isoquinolines
• quinocarcin

Topics

• Adenocarcinoma (pathology)
• Antibiotics, Antineoplastic (pharmacology)
• Colony-Forming Units Assay
• Drug Resistance
• Drug Screening Assays, Antitumor
• Humans
• Isoquinolines (pharmacology)
• Lung Neoplasms (pathology)
• Tumor Stem Cell Assay