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 |
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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. |
doi_str_mv | 10.1097/00001813-199306000-00013 |
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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. 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.</description><identifier>ISSN: 0959-4973</identifier><identifier>EISSN: 1473-5741</identifier><identifier>DOI: 10.1097/00001813-199306000-00013</identifier><identifier>PMID: 8395259</identifier><language>eng</language><publisher>England: Lippincott-Raven Publishers</publisher><subject>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</subject><ispartof>Anti-cancer drugs, 1993-06, Vol.4 (3), p.365-368</ispartof><rights>Lippincott-Raven Publishers.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8395259$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hand, Anne</creatorcontrib><creatorcontrib>Pelin, Katarina</creatorcontrib><creatorcontrib>Halme, Maija</creatorcontrib><creatorcontrib>Ekman, Anna</creatorcontrib><creatorcontrib>Mattson, Madeleine</creatorcontrib><creatorcontrib>Vallas, Marjatta</creatorcontrib><creatorcontrib>Mattson, Karin</creatorcontrib><creatorcontrib>Linnainmaa, Kaija</creatorcontrib><creatorcontrib>Husgafvel-Pursiainen, Kirsti</creatorcontrib><title>Interferon-α and interferon-γ combined with chemotherapy: in vitro sensitivity studies in non-small cell lung cancer cell lines</title><title>Anti-cancer drugs</title><addtitle>Anticancer Drugs</addtitle><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.</description><subject>Adenocarcinoma - drug therapy</subject><subject>Antineoplastic Combined Chemotherapy Protocols - pharmacology</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Cisplatin - administration & dosage</subject><subject>Cisplatin - pharmacology</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Drug Synergism</subject><subject>Etoposide - administration & dosage</subject><subject>Etoposide - pharmacology</subject><subject>Humans</subject><subject>Interferon Type I - administration & dosage</subject><subject>Interferon-gamma - administration & dosage</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Recombinant Proteins</subject><subject>Tumor Cells, Cultured - drug effects</subject><issn>0959-4973</issn><issn>1473-5741</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1OwzAUhC0EKqVwBCRfIGDHcWKzQxU_lSqxgbXl2C8kkDiVnVJ1yZEQ9-BMuLRUbPDC1pt5M4vPCGFKLiiRxSWJhwrKEiolI3mcko3CDtCYZgVLeJHRQzQmksskkwU7RichvMSVqLMRGgkmecrlGL3P3AC-At-75OsDa2dx80f5xKbvysaBxatmqLGpoeuHGrxerK_iJn5rBt_jAC40QxOHNQ7D0jYQNqaLFaHTbYsNxKtdumdstDPgd0IsDqfoqNJtgLPdO0FPtzeP0_tk_nA3m17PE5NSzhIQVpRSEM0BCKUcpMjzlJa6MkWZ50UlrM6szJlMKwE2qtxqUpV5SU0qQbAJEtte4_sQPFRq4ZtO-7WiRG2gql-oag9V_UCN0fNtdLEsO7D74I5i9LOtv-rbyC68tssVeFWDboda_fdX7BsJFoZ-</recordid><startdate>199306</startdate><enddate>199306</enddate><creator>Hand, Anne</creator><creator>Pelin, Katarina</creator><creator>Halme, Maija</creator><creator>Ekman, Anna</creator><creator>Mattson, Madeleine</creator><creator>Vallas, Marjatta</creator><creator>Mattson, Karin</creator><creator>Linnainmaa, Kaija</creator><creator>Husgafvel-Pursiainen, Kirsti</creator><general>Lippincott-Raven Publishers</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>199306</creationdate><title>Interferon-α and interferon-γ combined with chemotherapy: in vitro sensitivity studies in non-small cell lung cancer cell lines</title><author>Hand, Anne ; Pelin, Katarina ; Halme, Maija ; Ekman, Anna ; Mattson, Madeleine ; Vallas, Marjatta ; Mattson, Karin ; Linnainmaa, Kaija ; Husgafvel-Pursiainen, Kirsti</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2153-e8d8b980a5ee0115e986621bafc7b667f8da4d96392f8edfc75da0fb6b1c29e83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Adenocarcinoma - drug therapy</topic><topic>Antineoplastic Combined Chemotherapy Protocols - pharmacology</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Cisplatin - administration & dosage</topic><topic>Cisplatin - pharmacology</topic><topic>Drug Screening Assays, Antitumor</topic><topic>Drug Synergism</topic><topic>Etoposide - administration & dosage</topic><topic>Etoposide - pharmacology</topic><topic>Humans</topic><topic>Interferon Type I - administration & dosage</topic><topic>Interferon-gamma - administration & dosage</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Recombinant Proteins</topic><topic>Tumor Cells, Cultured - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hand, Anne</creatorcontrib><creatorcontrib>Pelin, Katarina</creatorcontrib><creatorcontrib>Halme, Maija</creatorcontrib><creatorcontrib>Ekman, Anna</creatorcontrib><creatorcontrib>Mattson, Madeleine</creatorcontrib><creatorcontrib>Vallas, Marjatta</creatorcontrib><creatorcontrib>Mattson, Karin</creatorcontrib><creatorcontrib>Linnainmaa, Kaija</creatorcontrib><creatorcontrib>Husgafvel-Pursiainen, Kirsti</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Anti-cancer drugs</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hand, Anne</au><au>Pelin, Katarina</au><au>Halme, Maija</au><au>Ekman, Anna</au><au>Mattson, Madeleine</au><au>Vallas, Marjatta</au><au>Mattson, Karin</au><au>Linnainmaa, Kaija</au><au>Husgafvel-Pursiainen, Kirsti</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interferon-α and interferon-γ combined with chemotherapy: in vitro sensitivity studies in non-small cell lung cancer cell lines</atitle><jtitle>Anti-cancer drugs</jtitle><addtitle>Anticancer Drugs</addtitle><date>1993-06</date><risdate>1993</risdate><volume>4</volume><issue>3</issue><spage>365</spage><epage>368</epage><pages>365-368</pages><issn>0959-4973</issn><eissn>1473-5741</eissn><abstract>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.</abstract><cop>England</cop><pub>Lippincott-Raven Publishers</pub><pmid>8395259</pmid><doi>10.1097/00001813-199306000-00013</doi><tpages>4</tpages></addata></record> |
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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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