» Articles » PMID: 1551172

Relations Between the Penetration, Binding and Average Concentration of Cytostatic Drugs in Human Tumour Spheroids

Overview
Specialty Oncology
Date 1992 Jan 1
PMID 1551172
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

A penetration assay based on freeze-drying and vapour fixation was applied to show the spatial distribution of non-bound and bound cytostatic drugs in cellular spheroids. Several studies have proposed that peripheral binding of drugs correlates with limited penetration. We showed that granular accumulation, mainly at the peripheral part of spheroids, might occur in parallel with good penetration. For example, this was the case in human glioma spheroids after incubation with Adriamycin for 15-30 min. Following treatment with actinomycin D, colon carcinoma spheroids exhibited rather good penetration but also showed granular accumulation mainly in their peripheral regions. Ara-C accumulated largely and homogeneously in the peripheral regions of colon carcinoma spheroids and this severely delayed penetration. It took about 1 h for ara-C in the central regions of the spheroids to reach the same concentration as in the culture medium. In contrast, ara-C easily penetrated glioma spheroids without accumulating noticeably at the periphery. Retention tests involving washing and further incubation in drug-free culture medium revealed that the areas demonstrating extensive accumulation most often retained the drug, indicating binding, whereas the concentration of drug in other areas decreased. The oil-centrifugation method, which was used for rapid separation of the spheroids from the drug-containing medium, showed that the average concentration of daunomycin in the spheroids exceeded that in the culture medium as early as after 15 min, by which time only limited penetration had occurred. We found that good penetration of ara-C correlated with a low average concentration in glioma spheroids, whereas limited penetration correlated with a high average concentration in colon carcinoma spheroids. The latter finding was attributable to the high accumulation of drug at the spheroid periphery. Thus, there was an inverse relationship between penetration and binding and between penetration and average drug concentration. It seemed that binding delayed or prevented penetration, whereas little, if any binding resulted in better penetration. Granular binding such as that observed Adriamycin and actinomycin D gave intermediately good penetration.

Citing Articles

Monolayer culture alters EGFR inhibitor response through abrogation of microRNA-mediated feedback regulation.

Florio A, Johnson S, Salvatori R, Vasmatzis G Sci Rep. 2024; 14(1):7303.

PMID: 38538642 PMC: 10973516. DOI: 10.1038/s41598-024-56920-7.


Effect of Gene Knockout on Drug Resistance in Paclitaxel and Topotecan Resistant Human Ovarian Cancer Cell Lines in 2D and 3D Model.

Nowacka M, Ginter-Matuszewska B, Swierczewska M, Sterzynska K, Nowicki M, Januchowski R Int J Mol Sci. 2022; 23(6).

PMID: 35328460 PMC: 8950618. DOI: 10.3390/ijms23063036.


The Profile of MicroRNA Expression and Potential Role in the Regulation of Drug-Resistant Genes in Cisplatin- and Paclitaxel-Resistant Ovarian Cancer Cell Lines.

Kazmierczak D, Jopek K, Sterzynska K, Nowicki M, Rucinski M, Januchowski R Int J Mol Sci. 2022; 23(1).

PMID: 35008952 PMC: 8745655. DOI: 10.3390/ijms23010526.


Lactic Acidosis Interferes With Toxicity of Perifosine to Colorectal Cancer Spheroids: Multimodal Imaging Analysis.

Pavlatovska B, Machalkova M, Brisudova P, Pruska A, Stepka K, Michalek J Front Oncol. 2020; 10:581365.

PMID: 33344237 PMC: 7746961. DOI: 10.3389/fonc.2020.581365.


A computational diffusion model to study antibody transport within reconstructed tumor microenvironments.

Cartaxo A, Almeida J, Gualda E, Marsal M, Loza-Alvarez P, Brito C BMC Bioinformatics. 2020; 21(1):529.

PMID: 33203360 PMC: 7672975. DOI: 10.1186/s12859-020-03854-2.


References
1.
Verstijnen C, Arends J, Moerkerk P, Geraedts J, Sekikawa K, Uitendaal M . The establishment and characterization of two new cell lines derived from a single human colonic adenocarcinoma. Virchows Arch B Cell Pathol Incl Mol Pathol. 1987; 53(4):191-7. DOI: 10.1007/BF02890243. View

2.
Westermark B, Ponten J, HUGOSSON R . Determinants for the establishment of permanent tissue culture lines from human gliomas. Acta Pathol Microbiol Scand A. 1973; 81(6):791-805. DOI: 10.1111/j.1699-0463.1973.tb03573.x. View

3.
Glimelius B, Norling B, Nederman T, Carlsson J . Extracellular matrices in multicellular spheroids of human glioma origin: increased incorporation of proteoglycans and fibronectin as compared to monolayer cultures. APMIS. 1988; 96(5):433-44. DOI: 10.1111/j.1699-0463.1988.tb05327.x. View

4.
Freyer J . Role of necrosis in regulating the growth saturation of multicellular spheroids. Cancer Res. 1988; 48(9):2432-9. View

5.
Durand R . Flow cytometry studies of intracellular adriamycin in multicell spheroids in vitro. Cancer Res. 1981; 41(9 Pt 1):3495-8. View