Skip to main content
Log in

Digital cell image analysis of verapamil-induced effects in chemosensitive and chemoresistant neoplastic cell lines

  • Original Papers
  • Experimental Oncology
  • Published:
Journal of Cancer Research and Clinical Oncology Aims and scope Submit manuscript

Abstract

We used chemosensitive and chemoresistant variants of the neoplastic mouse MXT mammary and human J82 and T24 bladder cell lines to characterize verapamil-induced cell proliferation and morphonuclear modifications in drug-treated and untreated cells. Chemoresistance to vinorelbine (Navelbine, aVinca alkaloid derivative), to DIAM3 (an investigational alkylating compound) and to Adriamycin (an intercalating agent) in the presence or absence of verapamil was monitored by means of the colorimetric 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. The results showed that verapamil restored a significant level of chemosensitivity in doses such as 1 μM or 10 μM in the three chemoresistant variants. The digital cell image analysis of Feulgen-stained T24-resistant cell nuclei revealed that verapamil restored the drug-treated cell kinetics and morphonuclear features observed in the sensitive counterpart especially with respect to the effects of adriamycin. Interestingly, verapamil induced a highly significant chromatin decondensation in resistant but not in sensitive variants. Such verapamil-induced decondensation may favour the accessibility of drugs to their DNA targets. Therefore, in addition to the well-known action of the drug on the influx of a cytotoxic compound from the cellular to the intracellular compartment, verapamil might also favour the accessibility of the nucleus, to the drug.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

Pgp:

P glycoprotein

MTT:

3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide

R:

resistant

S:

sensitive

A ini :

integrated absorbance

References

  • Akiyama SI, Cornwell MM, Kuwano M, Pastan I, Gottesman MM (1988) Most drugs that reverse multidrug resistance also inhibit photoaffinity labeling of P-glycoprotein by a vinblastine analog. Mol Pharmacol 33:144–147

    Google Scholar 

  • Bartels PH (1983) Numerical evaluation of cytologic data. Bivariate distributions and Bayesian decision boundary. Anal Quant Cytol Histol 2:77–83

    Google Scholar 

  • Beck WT (1990) Mechanisms of multidrug resistance in human tumor cells. The role of P-glycoprotein, DNA topoisomerase II and other factors. Cancer Treat Rev 17 [Suppl A]:11–20

    Google Scholar 

  • Bellamy WT, Dalton WS, Kailey JM, Gleason MC, McCloskey TM, Dorr RT, Alberts DS (1988) Verapamil reversal of doxorubicin resistance in multidrug-resistant human myeloma cells and association with drug accumulation and DNA damage. Cancer Res 48:6303–6308

    Google Scholar 

  • Bhalla K, Hindenburg A, Taub RN, Grant S (1985) Isolation and characterization of an anthracycline-resistant human leukemic cell line. Cancer Res 45:3657–3662

    Google Scholar 

  • Bhuyan BK, Smith KS, Kelly RC, Adams EG, Abraham I, Sampson KE (1993) Multidrug resistance is a component of V79 cell resistance to the alkylating agent adozelesin. Cancer Res 53:1354–1359

    Google Scholar 

  • Brugal G, Garbay C, Giroud F, Adhel D (1979) A double scanning microphotometer for image analysis: hardware, software and biomedical applications. J Histochem Cytochem 27:144–152

    Google Scholar 

  • Bubenik J, Baresova J, Jakoubkova J, Sainerova H, Donner J (1973) Etablished cell line of urinary bladder carcinoma (T24) containing tumour-sspecific antigen. Int J Cancer 11:765–773

    Google Scholar 

  • Carmichael C, De Graff WG, Gazdar AF, Minna D, Mitchell B (1987) Evaluation of a tetrazolium-based semiautomated colorimetric assay: assessment of chemosensitivity testing. Cancer Res 47:936–942

    Google Scholar 

  • Chauffert B, Martin F, Caignard A, Jeannin JF, Lecler A (1984) Cytofluorescence localization of Adriamycin in resistant colon cancer cells. Cancer Chemother Pharmacol 13:14–18

    Google Scholar 

  • Colomb E, Dussert C, Martin PM (1991) Nuclear texture parameters as discriminant factors in cell cycle effect and drug sensitivity studies. Cytometry 12:119–126

    Google Scholar 

  • Dufer J, Akeli MG, Jeannesson P, Desplaces A, Jardillier JC (1989) Quantitative morphological analysis of Adriamycin resistant human K562 leukemic cells. Cytometry 10:37–43

    Google Scholar 

  • Etiévant C, Kruczynski A, Pauwels O, Kiss R (1991) The combination of the tetrazolium derivative reduction (MTT) and digital cell image analysis to monitor in vitro the cytotoxicity of anti-neoplastic drugs. Anticancer Res 11:305–312.

    Google Scholar 

  • Ford JM, Hait WN (1990) Pharmacology of drugs that alter multidrug resistance in cancer. Pharmacol Rev 42:155–199

    Google Scholar 

  • Foxwell BMJ, Mackie A, Ling V, Ryffel B (1989) Identification of the multidrug resistance related P-glycoprotein as a cyclosporine binding protein. Mol Pharmacol 36:543–546

    Google Scholar 

  • Galloway MM (1975) Texture analysis using gray run lengths. Comput Graph Image Proc 4:172–179

    Google Scholar 

  • Giavazzi R, Scholar E, Hart IR (1982) Isolation and preliminary characterization of an Adriamycin-resistant murine fibrosarcoma cell line. Cancer Res 43:2216–2222

    Google Scholar 

  • Haralick RM, Shanmugam T, Dinstein I (1973) Textural features for image classification. IEE Trans Syst Man Cybern SMC 3:610–620

    Google Scholar 

  • Hunter T, Karin M (1972) The regulation of transcription by phosphorylation. Cell 70:375–387

    Google Scholar 

  • Juliano RL, Ling V (1976) A surface glycoprotein modulating drug permeability in chinese hamster ovary cell mutants. Biochem Biophys Acta 455:152–162

    Google Scholar 

  • Kalken CK van, Pinedo HM, Giaccone G (1991) Multidrug resistance from the clinical point of view. Eur J Cancer 27:1481–1486

    Google Scholar 

  • Kaye SB (1990) Reversal of multidrug resistance. Cancer Treat Rev 17:37–43

    Google Scholar 

  • Keizer HG, Schuurhuis GJ, Broxterman HJ, Lankelma J, Schoonen WGEJ, Rijn J van, Pinedo HM, Joenje H (1989) Correlation of multidrug resistance with decreased drug accumulation, altered subcellular drug distribution, and increased P-glycoprotein expression in cultured SW-1573 human lung tumor cells. Cancer Res 49:2988–2993

    Google Scholar 

  • Kiss R, Devleeschouwer N, Paridaens R, Danguy A, Atassi G (1986) Phenotypic change of the transplantable MXT mammary adenocarcinoma into mixed bone producing sarcoma-like tumors. Anticancer Res 6:753–760

    Google Scholar 

  • Kiss R, Launoit Y de, Danguy A, Paridaens R, Pasteels JL (1989) Influence of pituitary grafts or prolactin administrations on the hormone sensitivity of ovarian hormone-independent mouse mammary MXT tumors. Cancer Res 49:2945–2951

    Google Scholar 

  • Klohs W, Steinkampf RW (1988) Possible link between the intrinsic drug resistance of colon tumors and a detoxification mechanism of intestinal cells. Cancer Res 48:3025–3030

    Google Scholar 

  • Kramer RA, Zaher J, Kim G (1988) Role of the glutathione redox cycle in acquired and de novo multidrug resistance. Science 241:694–697

    Google Scholar 

  • Labarre JF (1985) Natural polyamines linked cyclophosphazenes. Attempts as the production of more selective antitumorals. Topic Curr Chem 129:173–260

    Google Scholar 

  • Launoit Y de, Kiss R (1989) In vivo influence of androgens on the cell kinetics and chromatin pattern of the MXT mouse mammary tumor treated or not by aminogluthetimide. J Cancer Res Clin Oncol 115:129–138

    Google Scholar 

  • Launoit Y de, Kiss R, Danguy A (1990) Influence of smear preparation and fixatives on the DNA ploidy and the morphonuclear features of the MXT mammary tumor and normal tissues in the mouse. Cytometry 11:691–699

    Google Scholar 

  • Marquardt D, Center MS (1992) Drug transport mechanisms in HL60cells isolated for resistance to Adriamycin: evidence for nuclear drug accumulation and redistribution in resistant cells. Cancer Res 52:3157–3163

    Google Scholar 

  • Mosman T (1983) Rapid colorimetric assay for cellular growth and survival application and cytotoxicity assay. J Immunol Methods 65:55–63

    Google Scholar 

  • O'Toole C, Price ZH, Ohnuki Y, Unsgaard B (1978) Ultrastructure, kariology and immunology of a cell line originated from a cell line originated from a human transitional-cell carcinoma. Br J Cancer 38:64–76

    Google Scholar 

  • Pastan I, Gottesman MM (1991) Multidrug resistance. Annu Rev Med 42:277–286

    Google Scholar 

  • Pauwels I, Kiss R (1991) Digital morphonuclear analyses of sensitive versus resistant neoplastic cells to vinca-alkaloid, alkylating, and intercalating drugs. Cytometry 12:388–397

    Google Scholar 

  • Pauwels O, Kiss R (1993) Monitoring of chemotherapy-induced morphonuclear modifications by means of digital cell image analysis. J Cancer Res Clin Oncol 119:533–540

    Google Scholar 

  • Pommier Y, Swartz RE, Zwelling LA, Kettigan D, Mattern MR, Charcosset JY, Jacquemin-Sablon A, Kohn KW (1986) Reduced formation of protein-associated DNA strand breaks in chinese hamster cells resistant to topoisomerase II inhibitors. Cancer Res 46:611–616

    Google Scholar 

  • Rao PN (1980) The molecular basis of drug induced G2 arrest in mammalian cells. Mol Cell Biochem 29:47–57

    Google Scholar 

  • Scheper RJ, Broxterman HJ, Scheffer GL, Kaaijk P, Dalton WS, Heijningen THM van, Kalken CK van, Slovak MJ, De Vries EGE, Valk P van der, Meijer CJLM, Pinedo HM (1993) Overexpression of a Mr 110,000 vesicular protein in non-P-glycoprotein-mediated multidrug resistance. Cancer Res 53:1475–1479

    Google Scholar 

  • Schuurhuis GS, Broxterman HJ, Cervantes A, Heijningen THM van, Lange JHM de, Baak JPA, Pinedo HM, Lankelma J (1989) Quantitative determination of factors contributing to doxorubicin resistance in multidrug-resistance cells. J Natl Cancer Inst 81:1887–1892

    Google Scholar 

  • Siegfried JM, Tritton TR, Sartorelli AC (1983) Comparison of anthracycline concentrations in S180 cell lines of varying sensitivity. Eur J Cancer Clin Oncol 19:1133–1141

    Google Scholar 

  • Tew KD, Clapper ML (1987) Glutathione S-transferase and anticancer drug resistance. In: Wooley PV, Tew KD (eds) Mechanisms of drug resistance in neoplasmic cells. Academic Press, Orlando, pp 141–157

    Google Scholar 

  • Tsuruo T, Iida H, Tsukagoshi S, Sakurai Y (1981) Overcoming vincristine resistance in P388 leukemia in vivo and in vitro through enhanced cytotoxicity of vincristine and vinblastine by verapamil. Cancer Res 41:1967–1972

    Google Scholar 

  • Waring J (1981) DNA modification and cancer. Annu Rev Biochem 50:159–192

    Google Scholar 

  • Willingham MC, Cornwell MM, Cardarelli CO, Gottesman MM, Pastan I (1986) Single cell analysis of daunomycin uptake and efflux in multidrug resistant and sensitive KB cells: effects of verapamil and other drugs. Cancer Res 46:5941–5946

    Google Scholar 

  • Yalowich JC, Ross WE (1984) Potentiation of etoposide induced DNA damage by calcium antagonists in L1210 cells in vitro. Cancer Res 44:3360–3365

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Holder of a grant from the Fonds National de la Recherche Scientifique (FNRS, Belgium)

Research Associate with the FNRS, Belgium

Rights and permissions

Reprints and permissions

About this article

Cite this article

Etiévant, C., Pauwels, O. & Kiss, R. Digital cell image analysis of verapamil-induced effects in chemosensitive and chemoresistant neoplastic cell lines. J Cancer Res Clin Oncol 120, 76–84 (1993). https://doi.org/10.1007/BF01200728

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01200728

Key words

Navigation