Biological and Clinical Implication of Neuron-Specific Enolase and Creatine Kinase BB in Small Cell Lung Cancer
The specificity of neuron-specific enolase (NSE) and creatine kinase BB (CK-BB) for small cell lung cancer (SCLC) was determined by biological and immunohistochemical procedures in lung cancer tissues and cultured cell lines. Average values of extractable NSE and CK-BB of SCLC tissues were significa...
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Veröffentlicht in: | Japanese journal of clinical oncology 1986-09, Vol.16 (3), p.213-221 |
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creator | ARIYOSHI, YUTAKA KATO, KANEFUSA UEDA, RYUZO TAKAHASHI, TAKASHI SATO, TSUNEKO AKATSUKA, HIROMICHI KUWABARA, MASAKI KITO, KUNIYOSHI SUCHI, TAIZAN NISHIMURA, MINORU SUGIURA, TAKAHIKO URATA, ATSUO OTA, KAZUO |
description | The specificity of neuron-specific enolase (NSE) and creatine kinase BB (CK-BB) for small cell lung cancer (SCLC) was determined by biological and immunohistochemical procedures in lung cancer tissues and cultured cell lines. Average values of extractable NSE and CK-BB of SCLC tissues were significantly higher than those of non-SCLC and normal lung tissues. A large amount of NSE and CK-BB was demonstrated in SCLC cell lines. Immunohistochemical examination showed positive staining for NSE and CK-BB in most cases of SCLC and in a few cases of non-SCLC. From these data NSE and CK-BB should be considered to be highly specific for SCLC. In a clinical study serum values exceeding 10 ng/ml for NSE and 1.5 ng/ml for CK-BB were set as positive for the enzymes. Positive rates in SCLC were 71.4% for NSE and 65.3% for CK-BB, which were significantly higher than those in non-SCLC. All positive cases were in an advanced stage. Consecutive daily NSE determinations during induction chemotherapy showed transient elevation immediately after the initiation of drug administration (tumor lysis syndrome), followed by a decline to the normal range in responders. This phe nomenon seems to indicate tumor sensitivity to cytotoxic drugs. NSE positive non-SCLC was as sensitive to cytotoxic drugs as SCLC. These findings indicate that lung cancer with elevated serum NSE and CK-BB levels at diagnosis should be strongly suspected of being SCLC in the advanced stage. |
doi_str_mv | 10.1093/oxfordjournals.jjco.a039145 |
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Average values of extractable NSE and CK-BB of SCLC tissues were significantly higher than those of non-SCLC and normal lung tissues. A large amount of NSE and CK-BB was demonstrated in SCLC cell lines. Immunohistochemical examination showed positive staining for NSE and CK-BB in most cases of SCLC and in a few cases of non-SCLC. From these data NSE and CK-BB should be considered to be highly specific for SCLC. In a clinical study serum values exceeding 10 ng/ml for NSE and 1.5 ng/ml for CK-BB were set as positive for the enzymes. Positive rates in SCLC were 71.4% for NSE and 65.3% for CK-BB, which were significantly higher than those in non-SCLC. All positive cases were in an advanced stage. Consecutive daily NSE determinations during induction chemotherapy showed transient elevation immediately after the initiation of drug administration (tumor lysis syndrome), followed by a decline to the normal range in responders. This phe nomenon seems to indicate tumor sensitivity to cytotoxic drugs. NSE positive non-SCLC was as sensitive to cytotoxic drugs as SCLC. 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Average values of extractable NSE and CK-BB of SCLC tissues were significantly higher than those of non-SCLC and normal lung tissues. A large amount of NSE and CK-BB was demonstrated in SCLC cell lines. Immunohistochemical examination showed positive staining for NSE and CK-BB in most cases of SCLC and in a few cases of non-SCLC. From these data NSE and CK-BB should be considered to be highly specific for SCLC. In a clinical study serum values exceeding 10 ng/ml for NSE and 1.5 ng/ml for CK-BB were set as positive for the enzymes. Positive rates in SCLC were 71.4% for NSE and 65.3% for CK-BB, which were significantly higher than those in non-SCLC. All positive cases were in an advanced stage. Consecutive daily NSE determinations during induction chemotherapy showed transient elevation immediately after the initiation of drug administration (tumor lysis syndrome), followed by a decline to the normal range in responders. This phe nomenon seems to indicate tumor sensitivity to cytotoxic drugs. NSE positive non-SCLC was as sensitive to cytotoxic drugs as SCLC. These findings indicate that lung cancer with elevated serum NSE and CK-BB levels at diagnosis should be strongly suspected of being SCLC in the advanced stage.</description><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Carcinoma, Non-Small-Cell Lung - enzymology</subject><subject>Carcinoma, Small Cell - drug therapy</subject><subject>Carcinoma, Small Cell - enzymology</subject><subject>Cell Line</subject><subject>Creatine Kinase - metabolism</subject><subject>Histocytochemistry</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Isoenzymes</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - enzymology</subject><subject>Phosphopyruvate Hydratase - metabolism</subject><issn>0368-2811</issn><issn>1465-3621</issn><issn>1465-3621</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkFtr4zAQhUXZ0k0vP2FBsLBvTnWxJZs-bby9h_YhLZS-CFkeF6W2lJViaP99lSYUikDS6JyjGT6EflMypaTip_6t86Fd-jE43cfpcmn8VBNe0bzYQxOaiyLjgtEfaEK4KDNWUvoTHca4JIQUZS4P0AEnjBFOJ8jPrO_9izW6x9q1uO6t-yyuh1WfLmvrHfYdvoMxeJctVmBsZw0-d77XEbaZAMnnAN9at3mbzbB1eDHovsc1pG0-uhdca2cgHKP9Lg0NJ7vzCD1enD_UV9n8_vK6_jvPDKvKdQbADDSs1bppBSUF0WlVwKGiLROykVzzZGzzvCqlkYWEstUNF50WFSOi5Efoz_bfVfD_R4hrNdho0jDagR-jkpJylpdFMp5tjSb4GAN0ahXsoMO7okRtcKvvuNUGt9rhTulfuzZjM0D7ld3xTXq21W1cw9uXrMOrEpLLQl09Pav8rqaL2383quAfejuSAw</recordid><startdate>19860901</startdate><enddate>19860901</enddate><creator>ARIYOSHI, YUTAKA</creator><creator>KATO, KANEFUSA</creator><creator>UEDA, RYUZO</creator><creator>TAKAHASHI, TAKASHI</creator><creator>SATO, TSUNEKO</creator><creator>AKATSUKA, HIROMICHI</creator><creator>KUWABARA, MASAKI</creator><creator>KITO, KUNIYOSHI</creator><creator>SUCHI, TAIZAN</creator><creator>NISHIMURA, MINORU</creator><creator>SUGIURA, TAKAHIKO</creator><creator>URATA, ATSUO</creator><creator>OTA, KAZUO</creator><general>Oxford University Press</general><scope>BSCLL</scope><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>7X8</scope></search><sort><creationdate>19860901</creationdate><title>Biological and Clinical Implication of Neuron-Specific Enolase and Creatine Kinase BB in Small Cell Lung Cancer</title><author>ARIYOSHI, YUTAKA ; KATO, KANEFUSA ; UEDA, RYUZO ; TAKAHASHI, TAKASHI ; SATO, TSUNEKO ; AKATSUKA, HIROMICHI ; KUWABARA, MASAKI ; KITO, KUNIYOSHI ; SUCHI, TAIZAN ; NISHIMURA, MINORU ; SUGIURA, TAKAHIKO ; URATA, ATSUO ; OTA, KAZUO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c298t-ee2ceb2daabd61050a0a09e3e91d267b73a3298d44987c757e8dab36fa6920683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Carcinoma, Non-Small-Cell Lung - enzymology</topic><topic>Carcinoma, Small Cell - drug therapy</topic><topic>Carcinoma, Small Cell - enzymology</topic><topic>Cell Line</topic><topic>Creatine Kinase - metabolism</topic><topic>Histocytochemistry</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Isoenzymes</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - enzymology</topic><topic>Phosphopyruvate Hydratase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ARIYOSHI, YUTAKA</creatorcontrib><creatorcontrib>KATO, KANEFUSA</creatorcontrib><creatorcontrib>UEDA, RYUZO</creatorcontrib><creatorcontrib>TAKAHASHI, TAKASHI</creatorcontrib><creatorcontrib>SATO, TSUNEKO</creatorcontrib><creatorcontrib>AKATSUKA, HIROMICHI</creatorcontrib><creatorcontrib>KUWABARA, MASAKI</creatorcontrib><creatorcontrib>KITO, KUNIYOSHI</creatorcontrib><creatorcontrib>SUCHI, TAIZAN</creatorcontrib><creatorcontrib>NISHIMURA, MINORU</creatorcontrib><creatorcontrib>SUGIURA, TAKAHIKO</creatorcontrib><creatorcontrib>URATA, ATSUO</creatorcontrib><creatorcontrib>OTA, KAZUO</creatorcontrib><collection>Istex</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>Japanese journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ARIYOSHI, YUTAKA</au><au>KATO, KANEFUSA</au><au>UEDA, RYUZO</au><au>TAKAHASHI, TAKASHI</au><au>SATO, TSUNEKO</au><au>AKATSUKA, HIROMICHI</au><au>KUWABARA, MASAKI</au><au>KITO, KUNIYOSHI</au><au>SUCHI, TAIZAN</au><au>NISHIMURA, MINORU</au><au>SUGIURA, TAKAHIKO</au><au>URATA, ATSUO</au><au>OTA, KAZUO</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biological and Clinical Implication of Neuron-Specific Enolase and Creatine Kinase BB in Small Cell Lung Cancer</atitle><jtitle>Japanese journal of clinical oncology</jtitle><addtitle>Jpn J Clin Oncol</addtitle><date>1986-09-01</date><risdate>1986</risdate><volume>16</volume><issue>3</issue><spage>213</spage><epage>221</epage><pages>213-221</pages><issn>0368-2811</issn><issn>1465-3621</issn><eissn>1465-3621</eissn><abstract>The specificity of neuron-specific enolase (NSE) and creatine kinase BB (CK-BB) for small cell lung cancer (SCLC) was determined by biological and immunohistochemical procedures in lung cancer tissues and cultured cell lines. Average values of extractable NSE and CK-BB of SCLC tissues were significantly higher than those of non-SCLC and normal lung tissues. A large amount of NSE and CK-BB was demonstrated in SCLC cell lines. Immunohistochemical examination showed positive staining for NSE and CK-BB in most cases of SCLC and in a few cases of non-SCLC. From these data NSE and CK-BB should be considered to be highly specific for SCLC. In a clinical study serum values exceeding 10 ng/ml for NSE and 1.5 ng/ml for CK-BB were set as positive for the enzymes. Positive rates in SCLC were 71.4% for NSE and 65.3% for CK-BB, which were significantly higher than those in non-SCLC. All positive cases were in an advanced stage. Consecutive daily NSE determinations during induction chemotherapy showed transient elevation immediately after the initiation of drug administration (tumor lysis syndrome), followed by a decline to the normal range in responders. This phe nomenon seems to indicate tumor sensitivity to cytotoxic drugs. NSE positive non-SCLC was as sensitive to cytotoxic drugs as SCLC. These findings indicate that lung cancer with elevated serum NSE and CK-BB levels at diagnosis should be strongly suspected of being SCLC in the advanced stage.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>3022031</pmid><doi>10.1093/oxfordjournals.jjco.a039145</doi><tpages>9</tpages></addata></record> |
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subjects | Antineoplastic Combined Chemotherapy Protocols - therapeutic use Carcinoma, Non-Small-Cell Lung - enzymology Carcinoma, Small Cell - drug therapy Carcinoma, Small Cell - enzymology Cell Line Creatine Kinase - metabolism Histocytochemistry Humans Immunoenzyme Techniques Isoenzymes Lung Neoplasms - drug therapy Lung Neoplasms - enzymology Phosphopyruvate Hydratase - metabolism |
title | Biological and Clinical Implication of Neuron-Specific Enolase and Creatine Kinase BB in Small Cell Lung Cancer |
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