Inter-experiment variation and dependence on culture conditions in assaying the chemosensitivity of human small cell lung cancer cell lines

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Standard

Inter-experiment variation and dependence on culture conditions in assaying the chemosensitivity of human small cell lung cancer cell lines. / Roed, H; Christensen, I B; Vindeløv, L L; Spang-Thomsen, M; Hansen, H H.

I: European journal of cancer & clinical oncology, Bind 23, Nr. 2, 1987, s. 177-86.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Roed, H, Christensen, IB, Vindeløv, LL, Spang-Thomsen, M & Hansen, HH 1987, 'Inter-experiment variation and dependence on culture conditions in assaying the chemosensitivity of human small cell lung cancer cell lines', European journal of cancer & clinical oncology, bind 23, nr. 2, s. 177-86.

APA

Roed, H., Christensen, I. B., Vindeløv, L. L., Spang-Thomsen, M., & Hansen, H. H. (1987). Inter-experiment variation and dependence on culture conditions in assaying the chemosensitivity of human small cell lung cancer cell lines. European journal of cancer & clinical oncology, 23(2), 177-86.

Vancouver

Roed H, Christensen IB, Vindeløv LL, Spang-Thomsen M, Hansen HH. Inter-experiment variation and dependence on culture conditions in assaying the chemosensitivity of human small cell lung cancer cell lines. European journal of cancer & clinical oncology. 1987;23(2):177-86.

Author

Roed, H ; Christensen, I B ; Vindeløv, L L ; Spang-Thomsen, M ; Hansen, H H. / Inter-experiment variation and dependence on culture conditions in assaying the chemosensitivity of human small cell lung cancer cell lines. I: European journal of cancer & clinical oncology. 1987 ; Bind 23, Nr. 2. s. 177-86.

Bibtex

@article{899e2c80654f11de8bc9000ea68e967b,
title = "Inter-experiment variation and dependence on culture conditions in assaying the chemosensitivity of human small cell lung cancer cell lines",
abstract = "Sensitivity of five human small cell lung cancer cell lines to doxorubicin was assessed by a double layer agar technique using two different bottom-layers. Neither of the bottom-layers provided proportionality between numbers of cells plated and numbers of colonies, but they were correlated by a logarithmic function. Even after correction for lack of proportionality the two assay systems provided significantly different dose-response curves. The stability of the chemosensitivity was tested after 25-30 weeks continuous in vitro culture or prolonged storage in liquid nitrogen. One cell line underwent significant changes after continuous in vitro culture whereas the cell lines tested after prolonged storage in liquid nitrogen showed only minor changes. It is concluded that instead of considering the concentration necessary to achieve a certain degree of cell kill (e.g. ID50) in one experiment on one cell line, dose-response curves obtained on several cell lines in different assay systems should be used in the evaluation of new drugs.",
author = "H Roed and Christensen, {I B} and Vindel{\o}v, {L L} and M Spang-Thomsen and Hansen, {H H}",
note = "Keywords: Carcinoma, Small Cell; Cell Line; Cell Survival; Colony-Forming Units Assay; Dose-Response Relationship, Drug; Doxorubicin; Drug Screening Assays, Antitumor; Humans; Lung Neoplasms; Mathematics; Tissue Preservation; Tumor Cells, Cultured",
year = "1987",
language = "English",
volume = "23",
pages = "177--86",
journal = "European Journal of Cancer and Clinical Oncology",
issn = "0277-5379",
publisher = "Pergamon Press",
number = "2",

}

RIS

TY - JOUR

T1 - Inter-experiment variation and dependence on culture conditions in assaying the chemosensitivity of human small cell lung cancer cell lines

AU - Roed, H

AU - Christensen, I B

AU - Vindeløv, L L

AU - Spang-Thomsen, M

AU - Hansen, H H

N1 - Keywords: Carcinoma, Small Cell; Cell Line; Cell Survival; Colony-Forming Units Assay; Dose-Response Relationship, Drug; Doxorubicin; Drug Screening Assays, Antitumor; Humans; Lung Neoplasms; Mathematics; Tissue Preservation; Tumor Cells, Cultured

PY - 1987

Y1 - 1987

N2 - Sensitivity of five human small cell lung cancer cell lines to doxorubicin was assessed by a double layer agar technique using two different bottom-layers. Neither of the bottom-layers provided proportionality between numbers of cells plated and numbers of colonies, but they were correlated by a logarithmic function. Even after correction for lack of proportionality the two assay systems provided significantly different dose-response curves. The stability of the chemosensitivity was tested after 25-30 weeks continuous in vitro culture or prolonged storage in liquid nitrogen. One cell line underwent significant changes after continuous in vitro culture whereas the cell lines tested after prolonged storage in liquid nitrogen showed only minor changes. It is concluded that instead of considering the concentration necessary to achieve a certain degree of cell kill (e.g. ID50) in one experiment on one cell line, dose-response curves obtained on several cell lines in different assay systems should be used in the evaluation of new drugs.

AB - Sensitivity of five human small cell lung cancer cell lines to doxorubicin was assessed by a double layer agar technique using two different bottom-layers. Neither of the bottom-layers provided proportionality between numbers of cells plated and numbers of colonies, but they were correlated by a logarithmic function. Even after correction for lack of proportionality the two assay systems provided significantly different dose-response curves. The stability of the chemosensitivity was tested after 25-30 weeks continuous in vitro culture or prolonged storage in liquid nitrogen. One cell line underwent significant changes after continuous in vitro culture whereas the cell lines tested after prolonged storage in liquid nitrogen showed only minor changes. It is concluded that instead of considering the concentration necessary to achieve a certain degree of cell kill (e.g. ID50) in one experiment on one cell line, dose-response curves obtained on several cell lines in different assay systems should be used in the evaluation of new drugs.

M3 - Journal article

C2 - 2832177

VL - 23

SP - 177

EP - 186

JO - European Journal of Cancer and Clinical Oncology

JF - European Journal of Cancer and Clinical Oncology

SN - 0277-5379

IS - 2

ER -

ID: 12871053