Clinical and in vitro response to 13-cis-retinoic acid in interferon-alpha resistant renal cell carcinoma
Retinoids are known to control many important biological processes, including differentiation, morphogenesis, growth and tissue homeostasis. More recently, clinical and pre-clinical results provide evidence for an antiproliferative effect of 13-cis-retinoic acid (13cRA) in interferon-alpha (IFN-alph...
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Veröffentlicht in: | Cancer biotherapy & radiopharmaceuticals 1997-01, Vol.12 (3), p.143-147 |
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creator | BUER, J PROBST, M DUENSING, S KÖDITZ, H FRANZKE, A DALLMANN, I GANSER, A ATZPODIEN, J |
description | Retinoids are known to control many important biological processes, including differentiation, morphogenesis, growth and tissue homeostasis. More recently, clinical and pre-clinical results provide evidence for an antiproliferative effect of 13-cis-retinoic acid (13cRA) in interferon-alpha (IFN-alpha) treated renal cell carcinoma patients. The manner in which 13cRA augments antitumor effects and modulates biologic and clinical responses of renal cell carcinoma to IFN-alpha remains elusive. In the present study, we report induction of apoptosis and objective tumor regression in response to 13cRA in advanced renal cell carcinoma patients refractory to IFN-alpha. Among 21 patients treated there were one complete and four partial remissions (objective response rate, 24%; median response duration 8+ months). Preliminary evidence suggests that 13cRA acid may reverse IFN-alpha resistance in renal cell carcinoma. |
doi_str_mv | 10.1089/cbr.1997.12.143 |
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More recently, clinical and pre-clinical results provide evidence for an antiproliferative effect of 13-cis-retinoic acid (13cRA) in interferon-alpha (IFN-alpha) treated renal cell carcinoma patients. The manner in which 13cRA augments antitumor effects and modulates biologic and clinical responses of renal cell carcinoma to IFN-alpha remains elusive. In the present study, we report induction of apoptosis and objective tumor regression in response to 13cRA in advanced renal cell carcinoma patients refractory to IFN-alpha. Among 21 patients treated there were one complete and four partial remissions (objective response rate, 24%; median response duration 8+ months). Preliminary evidence suggests that 13cRA acid may reverse IFN-alpha resistance in renal cell carcinoma.</description><identifier>ISSN: 1084-9785</identifier><identifier>EISSN: 1557-8852</identifier><identifier>DOI: 10.1089/cbr.1997.12.143</identifier><identifier>PMID: 10851460</identifier><identifier>CODEN: CBRAFJ</identifier><language>eng</language><publisher>Larchmont, NY: Liebert</publisher><subject>Aged ; Antineoplastic agents ; Apoptosis - drug effects ; Biological and medical sciences ; Carcinoma, Renal Cell - drug therapy ; Carcinoma, Renal Cell - pathology ; Female ; General aspects ; Humans ; Interferon-alpha - therapeutic use ; Isotretinoin - therapeutic use ; Kidney Neoplasms - drug therapy ; Kidney Neoplasms - pathology ; Male ; Medical sciences ; Middle Aged ; Pharmacology. 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More recently, clinical and pre-clinical results provide evidence for an antiproliferative effect of 13-cis-retinoic acid (13cRA) in interferon-alpha (IFN-alpha) treated renal cell carcinoma patients. The manner in which 13cRA augments antitumor effects and modulates biologic and clinical responses of renal cell carcinoma to IFN-alpha remains elusive. In the present study, we report induction of apoptosis and objective tumor regression in response to 13cRA in advanced renal cell carcinoma patients refractory to IFN-alpha. Among 21 patients treated there were one complete and four partial remissions (objective response rate, 24%; median response duration 8+ months). Preliminary evidence suggests that 13cRA acid may reverse IFN-alpha resistance in renal cell carcinoma.</description><subject>Aged</subject><subject>Antineoplastic agents</subject><subject>Apoptosis - drug effects</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Renal Cell - drug therapy</subject><subject>Carcinoma, Renal Cell - pathology</subject><subject>Female</subject><subject>General aspects</subject><subject>Humans</subject><subject>Interferon-alpha - therapeutic use</subject><subject>Isotretinoin - therapeutic use</subject><subject>Kidney Neoplasms - drug therapy</subject><subject>Kidney Neoplasms - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. 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Drug treatments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BUER, J</creatorcontrib><creatorcontrib>PROBST, M</creatorcontrib><creatorcontrib>DUENSING, S</creatorcontrib><creatorcontrib>KÖDITZ, H</creatorcontrib><creatorcontrib>FRANZKE, A</creatorcontrib><creatorcontrib>DALLMANN, I</creatorcontrib><creatorcontrib>GANSER, A</creatorcontrib><creatorcontrib>ATZPODIEN, J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cancer biotherapy & radiopharmaceuticals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BUER, J</au><au>PROBST, M</au><au>DUENSING, S</au><au>KÖDITZ, H</au><au>FRANZKE, A</au><au>DALLMANN, I</au><au>GANSER, A</au><au>ATZPODIEN, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical and in vitro response to 13-cis-retinoic acid in interferon-alpha resistant renal cell carcinoma</atitle><jtitle>Cancer biotherapy & radiopharmaceuticals</jtitle><addtitle>Cancer Biother Radiopharm</addtitle><date>1997-01-01</date><risdate>1997</risdate><volume>12</volume><issue>3</issue><spage>143</spage><epage>147</epage><pages>143-147</pages><issn>1084-9785</issn><eissn>1557-8852</eissn><coden>CBRAFJ</coden><abstract>Retinoids are known to control many important biological processes, including differentiation, morphogenesis, growth and tissue homeostasis. More recently, clinical and pre-clinical results provide evidence for an antiproliferative effect of 13-cis-retinoic acid (13cRA) in interferon-alpha (IFN-alpha) treated renal cell carcinoma patients. The manner in which 13cRA augments antitumor effects and modulates biologic and clinical responses of renal cell carcinoma to IFN-alpha remains elusive. In the present study, we report induction of apoptosis and objective tumor regression in response to 13cRA in advanced renal cell carcinoma patients refractory to IFN-alpha. Among 21 patients treated there were one complete and four partial remissions (objective response rate, 24%; median response duration 8+ months). Preliminary evidence suggests that 13cRA acid may reverse IFN-alpha resistance in renal cell carcinoma.</abstract><cop>Larchmont, NY</cop><pub>Liebert</pub><pmid>10851460</pmid><doi>10.1089/cbr.1997.12.143</doi><tpages>5</tpages></addata></record> |
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subjects | Aged Antineoplastic agents Apoptosis - drug effects Biological and medical sciences Carcinoma, Renal Cell - drug therapy Carcinoma, Renal Cell - pathology Female General aspects Humans Interferon-alpha - therapeutic use Isotretinoin - therapeutic use Kidney Neoplasms - drug therapy Kidney Neoplasms - pathology Male Medical sciences Middle Aged Pharmacology. Drug treatments |
title | Clinical and in vitro response to 13-cis-retinoic acid in interferon-alpha resistant renal cell carcinoma |
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