EFFECT OF THE QUASSINOIDS GLAUCARUBOLONE AND SIMALIKALACTONE D ON GROWTH OF CELLS PERMANENTLY INFECTED WITH FELINE AND HUMAN IMMUNODEFICIENCY VIRUSES AND ON VIRAL INFECTIONS

Growth of Crandall feline kidney cells permanently infected with feline immunodeficiency virus was inhibited by the anti-cancer quassinoid glaucarubolone whereas growth of uninfected cells was not inhibited. Similar results were obtained for human MOLT-4 cells infected with HIV-1. The results sugges...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Life sciences (1973) 1997-12, Vol.62 (3), p.213-219
Hauptverfasser: Morré, D.James, Zeichhardt, Heinz, Maxeiner, Hans-Günther, Grünert, Hans-Peter, Sawitzky, Dirk, Grieco, Paul
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 219
container_issue 3
container_start_page 213
container_title Life sciences (1973)
container_volume 62
creator Morré, D.James
Zeichhardt, Heinz
Maxeiner, Hans-Günther
Grünert, Hans-Peter
Sawitzky, Dirk
Grieco, Paul
description Growth of Crandall feline kidney cells permanently infected with feline immunodeficiency virus was inhibited by the anti-cancer quassinoid glaucarubolone whereas growth of uninfected cells was not inhibited. Similar results were obtained for human MOLT-4 cells infected with HIV-1. The results suggest that cell lines permanently infected with either the feline or the human lentivirus exhibit growth response characteristics to the quassinoids in common with other cell lines malignantly transformed. In addition the quassinoids may delay viral infection suggesting some commonality between the mechanism responsible for inhibition of the growth of the transformed phenotype and viral infection.
doi_str_mv 10.1016/S0024-3205(97)01089-8
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79713086</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0024320597010898</els_id><sourcerecordid>79713086</sourcerecordid><originalsourceid>FETCH-LOGICAL-c391t-42fa6a45591f4f3cdc5f8c461b21632ef9ae382a1544d9ea4b933923c3a0c9a63</originalsourceid><addsrcrecordid>eNqFkd1u0zAYhiMEGmVwCZN8hOAgYMf5sY-QSZzWwnWgSZh2ZLmOIwW160jaSbso7pGkjXa6I8v-nu95Jb-ed4PgFwRR_LWEMAh9HMDoE00-QwQJ9ckrb4FIQn0YY_TaWzwjb713w_AHQhhFCb7yrmhICKR04f3jec7TChQ5qFYc_KpZWQpViKwES8nqlG3q74UsFAdMZaAUaybFDyZZWk1vGSgUWG6K22o1GVIuZQl-8s2aKa4qeQeEmuw8A7diRHIuxWxa1SMDxHpdqyLjuUgFV-kd-C02dcnLMzKqxyuTs0QUqnzvvWnNbnAf5vPaq3NepStfFkuRMulbTNHRD4PWxCaMIorasMW2sVFLbBijbYBiHLiWGodJYFAUhg11JtxSjGmALTbQUhPja-_jxfvQH_6e3HDU-26wbrcz9-5wGnRCE4QheRmc4kJMyAhGF9D2h2HoXasf-m5v-ieNoJ761Oc-9VSWpok-96mnvZs54LTdu-Z5ay5wnH-7zN34HY-d6_VgO3dvXdP1zh51c-heSPgP78ShnA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16324388</pqid></control><display><type>article</type><title>EFFECT OF THE QUASSINOIDS GLAUCARUBOLONE AND SIMALIKALACTONE D ON GROWTH OF CELLS PERMANENTLY INFECTED WITH FELINE AND HUMAN IMMUNODEFICIENCY VIRUSES AND ON VIRAL INFECTIONS</title><source>Elsevier ScienceDirect Journals Complete - AutoHoldings</source><source>MEDLINE</source><creator>Morré, D.James ; Zeichhardt, Heinz ; Maxeiner, Hans-Günther ; Grünert, Hans-Peter ; Sawitzky, Dirk ; Grieco, Paul</creator><creatorcontrib>Morré, D.James ; Zeichhardt, Heinz ; Maxeiner, Hans-Günther ; Grünert, Hans-Peter ; Sawitzky, Dirk ; Grieco, Paul</creatorcontrib><description>Growth of Crandall feline kidney cells permanently infected with feline immunodeficiency virus was inhibited by the anti-cancer quassinoid glaucarubolone whereas growth of uninfected cells was not inhibited. Similar results were obtained for human MOLT-4 cells infected with HIV-1. The results suggest that cell lines permanently infected with either the feline or the human lentivirus exhibit growth response characteristics to the quassinoids in common with other cell lines malignantly transformed. In addition the quassinoids may delay viral infection suggesting some commonality between the mechanism responsible for inhibition of the growth of the transformed phenotype and viral infection.</description><identifier>ISSN: 0024-3205</identifier><identifier>EISSN: 1879-0631</identifier><identifier>DOI: 10.1016/S0024-3205(97)01089-8</identifier><identifier>PMID: 9488099</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>AIDS/HIV ; Animals ; Antineoplastic Agents, Phytogenic - pharmacology ; antiviral ; Cats ; Cell Division - drug effects ; Cell Transformation, Viral - drug effects ; feline immunodeficiency virus ; Glaucarubin - analogs &amp; derivatives ; Glaucarubin - pharmacology ; glaucarubolone ; HIV-1 ; HIV-1 - drug effects ; Humans ; Immunodeficiency Virus, Feline - drug effects ; NADH oxidase ; quassinoids ; Quassins ; simalikalactone D</subject><ispartof>Life sciences (1973), 1997-12, Vol.62 (3), p.213-219</ispartof><rights>1997 Elsevier Science Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c391t-42fa6a45591f4f3cdc5f8c461b21632ef9ae382a1544d9ea4b933923c3a0c9a63</citedby><cites>FETCH-LOGICAL-c391t-42fa6a45591f4f3cdc5f8c461b21632ef9ae382a1544d9ea4b933923c3a0c9a63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0024-3205(97)01089-8$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27911,27912,45982</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9488099$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Morré, D.James</creatorcontrib><creatorcontrib>Zeichhardt, Heinz</creatorcontrib><creatorcontrib>Maxeiner, Hans-Günther</creatorcontrib><creatorcontrib>Grünert, Hans-Peter</creatorcontrib><creatorcontrib>Sawitzky, Dirk</creatorcontrib><creatorcontrib>Grieco, Paul</creatorcontrib><title>EFFECT OF THE QUASSINOIDS GLAUCARUBOLONE AND SIMALIKALACTONE D ON GROWTH OF CELLS PERMANENTLY INFECTED WITH FELINE AND HUMAN IMMUNODEFICIENCY VIRUSES AND ON VIRAL INFECTIONS</title><title>Life sciences (1973)</title><addtitle>Life Sci</addtitle><description>Growth of Crandall feline kidney cells permanently infected with feline immunodeficiency virus was inhibited by the anti-cancer quassinoid glaucarubolone whereas growth of uninfected cells was not inhibited. Similar results were obtained for human MOLT-4 cells infected with HIV-1. The results suggest that cell lines permanently infected with either the feline or the human lentivirus exhibit growth response characteristics to the quassinoids in common with other cell lines malignantly transformed. In addition the quassinoids may delay viral infection suggesting some commonality between the mechanism responsible for inhibition of the growth of the transformed phenotype and viral infection.</description><subject>AIDS/HIV</subject><subject>Animals</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>antiviral</subject><subject>Cats</subject><subject>Cell Division - drug effects</subject><subject>Cell Transformation, Viral - drug effects</subject><subject>feline immunodeficiency virus</subject><subject>Glaucarubin - analogs &amp; derivatives</subject><subject>Glaucarubin - pharmacology</subject><subject>glaucarubolone</subject><subject>HIV-1</subject><subject>HIV-1 - drug effects</subject><subject>Humans</subject><subject>Immunodeficiency Virus, Feline - drug effects</subject><subject>NADH oxidase</subject><subject>quassinoids</subject><subject>Quassins</subject><subject>simalikalactone D</subject><issn>0024-3205</issn><issn>1879-0631</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkd1u0zAYhiMEGmVwCZN8hOAgYMf5sY-QSZzWwnWgSZh2ZLmOIwW160jaSbso7pGkjXa6I8v-nu95Jb-ed4PgFwRR_LWEMAh9HMDoE00-QwQJ9ckrb4FIQn0YY_TaWzwjb713w_AHQhhFCb7yrmhICKR04f3jec7TChQ5qFYc_KpZWQpViKwES8nqlG3q74UsFAdMZaAUaybFDyZZWk1vGSgUWG6K22o1GVIuZQl-8s2aKa4qeQeEmuw8A7diRHIuxWxa1SMDxHpdqyLjuUgFV-kd-C02dcnLMzKqxyuTs0QUqnzvvWnNbnAf5vPaq3NepStfFkuRMulbTNHRD4PWxCaMIorasMW2sVFLbBijbYBiHLiWGodJYFAUhg11JtxSjGmALTbQUhPja-_jxfvQH_6e3HDU-26wbrcz9-5wGnRCE4QheRmc4kJMyAhGF9D2h2HoXasf-m5v-ieNoJ761Oc-9VSWpok-96mnvZs54LTdu-Z5ay5wnH-7zN34HY-d6_VgO3dvXdP1zh51c-heSPgP78ShnA</recordid><startdate>19971212</startdate><enddate>19971212</enddate><creator>Morré, D.James</creator><creator>Zeichhardt, Heinz</creator><creator>Maxeiner, Hans-Günther</creator><creator>Grünert, Hans-Peter</creator><creator>Sawitzky, Dirk</creator><creator>Grieco, Paul</creator><general>Elsevier Inc</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><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19971212</creationdate><title>EFFECT OF THE QUASSINOIDS GLAUCARUBOLONE AND SIMALIKALACTONE D ON GROWTH OF CELLS PERMANENTLY INFECTED WITH FELINE AND HUMAN IMMUNODEFICIENCY VIRUSES AND ON VIRAL INFECTIONS</title><author>Morré, D.James ; Zeichhardt, Heinz ; Maxeiner, Hans-Günther ; Grünert, Hans-Peter ; Sawitzky, Dirk ; Grieco, Paul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c391t-42fa6a45591f4f3cdc5f8c461b21632ef9ae382a1544d9ea4b933923c3a0c9a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>AIDS/HIV</topic><topic>Animals</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>antiviral</topic><topic>Cats</topic><topic>Cell Division - drug effects</topic><topic>Cell Transformation, Viral - drug effects</topic><topic>feline immunodeficiency virus</topic><topic>Glaucarubin - analogs &amp; derivatives</topic><topic>Glaucarubin - pharmacology</topic><topic>glaucarubolone</topic><topic>HIV-1</topic><topic>HIV-1 - drug effects</topic><topic>Humans</topic><topic>Immunodeficiency Virus, Feline - drug effects</topic><topic>NADH oxidase</topic><topic>quassinoids</topic><topic>Quassins</topic><topic>simalikalactone D</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Morré, D.James</creatorcontrib><creatorcontrib>Zeichhardt, Heinz</creatorcontrib><creatorcontrib>Maxeiner, Hans-Günther</creatorcontrib><creatorcontrib>Grünert, Hans-Peter</creatorcontrib><creatorcontrib>Sawitzky, Dirk</creatorcontrib><creatorcontrib>Grieco, Paul</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Morré, D.James</au><au>Zeichhardt, Heinz</au><au>Maxeiner, Hans-Günther</au><au>Grünert, Hans-Peter</au><au>Sawitzky, Dirk</au><au>Grieco, Paul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EFFECT OF THE QUASSINOIDS GLAUCARUBOLONE AND SIMALIKALACTONE D ON GROWTH OF CELLS PERMANENTLY INFECTED WITH FELINE AND HUMAN IMMUNODEFICIENCY VIRUSES AND ON VIRAL INFECTIONS</atitle><jtitle>Life sciences (1973)</jtitle><addtitle>Life Sci</addtitle><date>1997-12-12</date><risdate>1997</risdate><volume>62</volume><issue>3</issue><spage>213</spage><epage>219</epage><pages>213-219</pages><issn>0024-3205</issn><eissn>1879-0631</eissn><abstract>Growth of Crandall feline kidney cells permanently infected with feline immunodeficiency virus was inhibited by the anti-cancer quassinoid glaucarubolone whereas growth of uninfected cells was not inhibited. Similar results were obtained for human MOLT-4 cells infected with HIV-1. The results suggest that cell lines permanently infected with either the feline or the human lentivirus exhibit growth response characteristics to the quassinoids in common with other cell lines malignantly transformed. In addition the quassinoids may delay viral infection suggesting some commonality between the mechanism responsible for inhibition of the growth of the transformed phenotype and viral infection.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>9488099</pmid><doi>10.1016/S0024-3205(97)01089-8</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0024-3205
ispartof Life sciences (1973), 1997-12, Vol.62 (3), p.213-219
issn 0024-3205
1879-0631
language eng
recordid cdi_proquest_miscellaneous_79713086
source Elsevier ScienceDirect Journals Complete - AutoHoldings; MEDLINE
subjects AIDS/HIV
Animals
Antineoplastic Agents, Phytogenic - pharmacology
antiviral
Cats
Cell Division - drug effects
Cell Transformation, Viral - drug effects
feline immunodeficiency virus
Glaucarubin - analogs & derivatives
Glaucarubin - pharmacology
glaucarubolone
HIV-1
HIV-1 - drug effects
Humans
Immunodeficiency Virus, Feline - drug effects
NADH oxidase
quassinoids
Quassins
simalikalactone D
title EFFECT OF THE QUASSINOIDS GLAUCARUBOLONE AND SIMALIKALACTONE D ON GROWTH OF CELLS PERMANENTLY INFECTED WITH FELINE AND HUMAN IMMUNODEFICIENCY VIRUSES AND ON VIRAL INFECTIONS
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-15T12%3A42%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=EFFECT%20OF%20THE%20QUASSINOIDS%20GLAUCARUBOLONE%20AND%20SIMALIKALACTONE%20D%20ON%20GROWTH%20OF%20CELLS%20PERMANENTLY%20INFECTED%20WITH%20FELINE%20AND%20HUMAN%20IMMUNODEFICIENCY%20VIRUSES%20AND%20ON%20VIRAL%20INFECTIONS&rft.jtitle=Life%20sciences%20(1973)&rft.au=Morr%C3%A9,%20D.James&rft.date=1997-12-12&rft.volume=62&rft.issue=3&rft.spage=213&rft.epage=219&rft.pages=213-219&rft.issn=0024-3205&rft.eissn=1879-0631&rft_id=info:doi/10.1016/S0024-3205(97)01089-8&rft_dat=%3Cproquest_cross%3E79713086%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16324388&rft_id=info:pmid/9488099&rft_els_id=S0024320597010898&rfr_iscdi=true