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A Methodological Approach to the Prediction of Anticancer Drug Effect in Humans

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TLDR
It was suggested that it may be possible to predict cancericidal drug activity for individual neoplasms by assays the tumor cells in vitro for drug sensitivity by assaying the tumor Cells in vitroFor drug sensitivity.
Abstract
Tumor cells from animals and humans were treated with drugs under tissue culture conditions. Tumor cells from the sensitive L1210 model were studied first. A dose-response curve was derived between drug exposure and subsequent cytotoxicity in L1210. The concentration of drug and duration of exposure were factors critical to the subsequent development of in vitro cytotoxicity. The in vitro dosage which effected 50% leukemic cell death in L1210 cells correlated with reported in vivo drug levels. Other tumor models and human neoplastic cells were studied at this dosage level. A good correlation was noted in these studies between the in vivo responsiveness and the in vitro chemotherapy results in both animals and humans. It was suggested by these results that it may be possible to predict cancericidal drug activity for individual neoplasms by assaying the tumor cells in vitro for drug sensitivity.

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Citations
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Gold(III) dithiocarbamate derivatives for the treatment of cancer: solution chemistry, DNA binding, and hemolytic properties.

TL;DR: These gold(III) complexes show high reactivity toward some biologically important isolated macromolecules, resulting in a dramatic inhibition of both DNA and RNA synthesis and inducing DNA lesions with a faster kinetics than cisplatin, suggesting that intracellular DNA might not represent their primary or exclusive biological target.
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A Novel Dye Exclusion Method for Testing in Vitro Chemosensitivity of Human Tumors

TL;DR: The assay results demonstrated a strong correlation between the in vitro chemosensitivity of different types of tumors and the known clinical response patterns of these tumors.
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Comparison of Dye Exclusion Assays with a Clonogenic Assay in the Determination of Drug-induced Cytotoxicity

TL;DR: A novel "ratio" method was found to be a more sensitive index of drug-induced cell kill than the traditional percent viability method and all three assays demonstrated a clear dose-effect relationship for most of the drugs tested.
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Platinum(II) and palladium(II) complexes with dithiocarbamates and amines: synthesis, characterization and cell assay

TL;DR: The [M(ESDT)Cl]n species have been reacted with various amines in dichloromethane or chloroform to obtain mixed ligand complexes and the dithiocarbamato intermediates have been tested for in vitro cytostatic activity against human leukemic HL-60 and HeLa cells.
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In vitro antitumor activity of the water soluble copper(I) complexes bearing the tris(hydroxymethyl)phosphine ligand.

TL;DR: Cytological stains and flow cytometric analyses indicated that the phosphine copper(I) complex is able to inhibit the growth of tumor cells via G2/M cell cycle arrest and paraptosis accompanied with the loss of mitochondrial transmembrane potential.
References
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Book

Tumors of the hematopoietic system

TL;DR: Reading tumors of the hematopoietic system is also a way as one of the collective books that gives many advantages.
Journal ArticleDOI

Quantitation of Differential Sensitivity of Human-Tumor Stem Cells to Anticancer Drugs

TL;DR: An in vitro tumor-colony assay developed to measure sensitity of human-tumor stem cells to anticancer drugs shows sufficient promise to warrant larger-scale testing to determine its efficacy for selection of new agents and individualized cancer chemotherapy regimens.
Journal ArticleDOI

Counting actively metabolizing tissue cultured cells.

TL;DR: In balanced salt solution 20 mg per cent of Erythrosin B differentially stained Strain L tissue culture cells, cells that were not stained respired and produced lactic acid did not metabolize.
Journal Article

Comparison of in vitro methods to determine drug-induced cell lethality.

TL;DR: Human lymphoma cell line was exposed in vitro to increasing concentrations of adriamycin, bleomycin, and 1,3-bis(2-chloroethyl)-1-nitrosourea for 1 hr, and CF appears as the most reliable, dose-dependent index of cell lethality.
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