Interferon-α and interferon-γ combined with chemotherapy: in vitro sensitivity studies in non-small cell lung cancer cell lines

Non-small cell lung cancers (NSCLC) are often resistant to chemotherapy. Cisplatin has shown the most activity against all the histological subtypes and is now used in most combined treatment programmes. Interferon (IFN)-α has been shown to potentiate cisplatin and other drugs experimentally and in...

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Veröffentlicht in:Anti-cancer drugs 1993-06, Vol.4 (3), p.365-368
Hauptverfasser: Hand, Anne, Pelin, Katarina, Halme, Maija, Ekman, Anna, Mattson, Madeleine, Vallas, Marjatta, Mattson, Karin, Linnainmaa, Kaija, Husgafvel-Pursiainen, Kirsti
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container_end_page 368
container_issue 3
container_start_page 365
container_title Anti-cancer drugs
container_volume 4
creator Hand, Anne
Pelin, Katarina
Halme, Maija
Ekman, Anna
Mattson, Madeleine
Vallas, Marjatta
Mattson, Karin
Linnainmaa, Kaija
Husgafvel-Pursiainen, Kirsti
description Non-small cell lung cancers (NSCLC) are often resistant to chemotherapy. Cisplatin has shown the most activity against all the histological subtypes and is now used in most combined treatment programmes. Interferon (IFN)-α has been shown to potentiate cisplatin and other drugs experimentally and in clinical trials involving NSCLC. We are looking at the responses of different NSCLC cell lines to cisplatin (P), etoposide (VP-16) and IFN [recombinant human IFN-α2c (IFN-α) and IFN-γb (IFN-γ)], individually and in combination. We then compare the results with those from a clinical trial of etoposide and cisplatin with interferon in advanced NSCLC. We report here the results from the first of our cell lines, established from a large cell anaplastic carcinoma. We have confirmed earlier findings that NSCLC cell lines are not sensitive to either IFN-α or IFN-γ alone. However a combination of IFN-α and IFN-γ does reduce cell proliferation in our cell lines. This IFN combination potentiates the response of the cells to etoposide far more than to cisplatin. There is a trend towards greater activity when a combination of cisplatin and etoposide is used, compared with the activity of either drug alone. This effect is further increased by the interferon combination.
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Cisplatin has shown the most activity against all the histological subtypes and is now used in most combined treatment programmes. Interferon (IFN)-α has been shown to potentiate cisplatin and other drugs experimentally and in clinical trials involving NSCLC. We are looking at the responses of different NSCLC cell lines to cisplatin (P), etoposide (VP-16) and IFN [recombinant human IFN-α2c (IFN-α) and IFN-γb (IFN-γ)], individually and in combination. We then compare the results with those from a clinical trial of etoposide and cisplatin with interferon in advanced NSCLC. We report here the results from the first of our cell lines, established from a large cell anaplastic carcinoma. We have confirmed earlier findings that NSCLC cell lines are not sensitive to either IFN-α or IFN-γ alone. However a combination of IFN-α and IFN-γ does reduce cell proliferation in our cell lines. This IFN combination potentiates the response of the cells to etoposide far more than to cisplatin. 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source MEDLINE; Journals@Ovid Complete
subjects Adenocarcinoma - drug therapy
Antineoplastic Combined Chemotherapy Protocols - pharmacology
Carcinoma, Non-Small-Cell Lung - drug therapy
Cisplatin - administration & dosage
Cisplatin - pharmacology
Drug Screening Assays, Antitumor
Drug Synergism
Etoposide - administration & dosage
Etoposide - pharmacology
Humans
Interferon Type I - administration & dosage
Interferon-gamma - administration & dosage
Lung Neoplasms - drug therapy
Recombinant Proteins
Tumor Cells, Cultured - drug effects
title Interferon-α and interferon-γ combined with chemotherapy: in vitro sensitivity studies in non-small cell lung cancer cell lines
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