Signaling Pathways in Adrenocortical Cancer
: Adrenocortical carcinoma is a rare tumor that carries a very poor prognosis. Despite efforts to develop new therapeutic regimens to treat this disease, surgery remains the mainstay of treatment. Laboratory studies of adrenocortical cancers have revealed a wide variety of signaling pathways that ca...
Gespeichert in:
Veröffentlicht in: | Annals of the New York Academy of Sciences 2002-06, Vol.968 (1), p.222-239 |
---|---|
1. Verfasser: | |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 239 |
---|---|
container_issue | 1 |
container_start_page | 222 |
container_title | Annals of the New York Academy of Sciences |
container_volume | 968 |
creator | KIRSCHNER, LAWRENCE S. |
description | : Adrenocortical carcinoma is a rare tumor that carries a very poor prognosis. Despite efforts to develop new therapeutic regimens to treat this disease, surgery remains the mainstay of treatment. Laboratory studies of adrenocortical cancers have revealed a wide variety of signaling pathways that can be altered in these neoplasms. Although ACTH signaling through adenylyl cyclase and protein kinase A is important for normal adrenal cellular physiology, there is evidence to suggest that this pathway may inhibit the growth of adrenocortical tumors, and that inactivation of the ACTH receptor may promote tumor formation. Although multiple signal transduction pathways are essential for normal adrenal growth and hormone secretion, efforts to identify events required for neoplastic transformation have met with limited success. Alterations that have frequently been observed in adrenocortical carcinoma include up‐regulation of the IGF‐II system, as well as mutations in TP53 and RAS. Current studies aim to elucidate the mechanisms of tumor growth by studying proproliferative signaling pathways, such as those involving Akt/PKB and the mitogen‐activated protein kinases (MAPKs). Although studies of single pathways have been helpful in guiding investigations, new tools to study the integration and multiplicity of signaling pathways hold the hope of improved understanding of the signaling pathway alterations in adrenocortical cancer. |
doi_str_mv | 10.1111/j.1749-6632.2002.tb04338.x |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71909108</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71909108</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4752-21b9ffdd5dc5a595bb68ea7abc92e20d042137d469d688639427a91ad59ad5053</originalsourceid><addsrcrecordid>eNqVkE1Lw0AQhhdRbK3-BQkevEjifiTZrBcpxbZCqYUqflyWze6mbk2TupvS9t-b0KBnB4Y5zDvPwAPAFYIBqut2GSAaMj-OCQ4whDioUhgSkgS7I9D9XR2DLoSU-gnDpAPOnFtCiHAS0lPQQRghhinrgpu5WRQiN8XCm4nqcyv2zjOF11dWF6UsbWWkyL2BKKS25-AkE7nTF-3sgZfhw_Ng7E-eRo-D_sSXIY2wj1HKskypSMlIRCxK0zjRgopUMqwxVDDEiFAVxkzFSRITFmIqGBIqYnXDiPTA9YG7tuX3RruKr4yTOs9FocuN4xQxyBBM6uDdISht6ZzVGV9bsxJ2zxHkjSq-5I0P3vjgjSrequK7-viy_bJJV1r9nbZu6sD9IbA1ud7_A82n7_05xrgm-AeCcZXe_RKE_eIxJTTir9MRn6K38RB-zPiI_AARAYdG</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>71909108</pqid></control><display><type>article</type><title>Signaling Pathways in Adrenocortical Cancer</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>KIRSCHNER, LAWRENCE S.</creator><creatorcontrib>KIRSCHNER, LAWRENCE S.</creatorcontrib><description>: Adrenocortical carcinoma is a rare tumor that carries a very poor prognosis. Despite efforts to develop new therapeutic regimens to treat this disease, surgery remains the mainstay of treatment. Laboratory studies of adrenocortical cancers have revealed a wide variety of signaling pathways that can be altered in these neoplasms. Although ACTH signaling through adenylyl cyclase and protein kinase A is important for normal adrenal cellular physiology, there is evidence to suggest that this pathway may inhibit the growth of adrenocortical tumors, and that inactivation of the ACTH receptor may promote tumor formation. Although multiple signal transduction pathways are essential for normal adrenal growth and hormone secretion, efforts to identify events required for neoplastic transformation have met with limited success. Alterations that have frequently been observed in adrenocortical carcinoma include up‐regulation of the IGF‐II system, as well as mutations in TP53 and RAS. Current studies aim to elucidate the mechanisms of tumor growth by studying proproliferative signaling pathways, such as those involving Akt/PKB and the mitogen‐activated protein kinases (MAPKs). Although studies of single pathways have been helpful in guiding investigations, new tools to study the integration and multiplicity of signaling pathways hold the hope of improved understanding of the signaling pathway alterations in adrenocortical cancer.</description><identifier>ISSN: 0077-8923</identifier><identifier>EISSN: 1749-6632</identifier><identifier>DOI: 10.1111/j.1749-6632.2002.tb04338.x</identifier><identifier>PMID: 12119279</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>ACTH receptor ; adrenal cancer ; Adrenal Cortex Neoplasms - physiopathology ; adrenocortical carcinoma ; Adrenocorticotropic Hormone - metabolism ; Cyclic AMP - metabolism ; Cyclic AMP-Dependent Protein Kinases - metabolism ; EGF ; G proteins ; Genes, ras - genetics ; growth factors ; Humans ; insulin-like growth factor ; Insulin-Like Growth Factor I - metabolism ; Insulin-Like Growth Factor II - metabolism ; mitogen-activated protein kinase (MAPK) ; p53 ; protein kinase A (PKA) ; ras ; Receptors, Cell Surface - metabolism ; signal transduction ; Signal Transduction - physiology ; Transcription Factors - metabolism ; Tumor Suppressor Protein p53 - genetics ; Tumor Suppressor Protein p53 - metabolism</subject><ispartof>Annals of the New York Academy of Sciences, 2002-06, Vol.968 (1), p.222-239</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4752-21b9ffdd5dc5a595bb68ea7abc92e20d042137d469d688639427a91ad59ad5053</citedby><cites>FETCH-LOGICAL-c4752-21b9ffdd5dc5a595bb68ea7abc92e20d042137d469d688639427a91ad59ad5053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1749-6632.2002.tb04338.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1749-6632.2002.tb04338.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12119279$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KIRSCHNER, LAWRENCE S.</creatorcontrib><title>Signaling Pathways in Adrenocortical Cancer</title><title>Annals of the New York Academy of Sciences</title><addtitle>Ann N Y Acad Sci</addtitle><description>: Adrenocortical carcinoma is a rare tumor that carries a very poor prognosis. Despite efforts to develop new therapeutic regimens to treat this disease, surgery remains the mainstay of treatment. Laboratory studies of adrenocortical cancers have revealed a wide variety of signaling pathways that can be altered in these neoplasms. Although ACTH signaling through adenylyl cyclase and protein kinase A is important for normal adrenal cellular physiology, there is evidence to suggest that this pathway may inhibit the growth of adrenocortical tumors, and that inactivation of the ACTH receptor may promote tumor formation. Although multiple signal transduction pathways are essential for normal adrenal growth and hormone secretion, efforts to identify events required for neoplastic transformation have met with limited success. Alterations that have frequently been observed in adrenocortical carcinoma include up‐regulation of the IGF‐II system, as well as mutations in TP53 and RAS. Current studies aim to elucidate the mechanisms of tumor growth by studying proproliferative signaling pathways, such as those involving Akt/PKB and the mitogen‐activated protein kinases (MAPKs). Although studies of single pathways have been helpful in guiding investigations, new tools to study the integration and multiplicity of signaling pathways hold the hope of improved understanding of the signaling pathway alterations in adrenocortical cancer.</description><subject>ACTH receptor</subject><subject>adrenal cancer</subject><subject>Adrenal Cortex Neoplasms - physiopathology</subject><subject>adrenocortical carcinoma</subject><subject>Adrenocorticotropic Hormone - metabolism</subject><subject>Cyclic AMP - metabolism</subject><subject>Cyclic AMP-Dependent Protein Kinases - metabolism</subject><subject>EGF</subject><subject>G proteins</subject><subject>Genes, ras - genetics</subject><subject>growth factors</subject><subject>Humans</subject><subject>insulin-like growth factor</subject><subject>Insulin-Like Growth Factor I - metabolism</subject><subject>Insulin-Like Growth Factor II - metabolism</subject><subject>mitogen-activated protein kinase (MAPK)</subject><subject>p53</subject><subject>protein kinase A (PKA)</subject><subject>ras</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>signal transduction</subject><subject>Signal Transduction - physiology</subject><subject>Transcription Factors - metabolism</subject><subject>Tumor Suppressor Protein p53 - genetics</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><issn>0077-8923</issn><issn>1749-6632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkE1Lw0AQhhdRbK3-BQkevEjifiTZrBcpxbZCqYUqflyWze6mbk2TupvS9t-b0KBnB4Y5zDvPwAPAFYIBqut2GSAaMj-OCQ4whDioUhgSkgS7I9D9XR2DLoSU-gnDpAPOnFtCiHAS0lPQQRghhinrgpu5WRQiN8XCm4nqcyv2zjOF11dWF6UsbWWkyL2BKKS25-AkE7nTF-3sgZfhw_Ng7E-eRo-D_sSXIY2wj1HKskypSMlIRCxK0zjRgopUMqwxVDDEiFAVxkzFSRITFmIqGBIqYnXDiPTA9YG7tuX3RruKr4yTOs9FocuN4xQxyBBM6uDdISht6ZzVGV9bsxJ2zxHkjSq-5I0P3vjgjSrequK7-viy_bJJV1r9nbZu6sD9IbA1ud7_A82n7_05xrgm-AeCcZXe_RKE_eIxJTTir9MRn6K38RB-zPiI_AARAYdG</recordid><startdate>200206</startdate><enddate>200206</enddate><creator>KIRSCHNER, LAWRENCE S.</creator><general>Blackwell Publishing Ltd</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>200206</creationdate><title>Signaling Pathways in Adrenocortical Cancer</title><author>KIRSCHNER, LAWRENCE S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4752-21b9ffdd5dc5a595bb68ea7abc92e20d042137d469d688639427a91ad59ad5053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>ACTH receptor</topic><topic>adrenal cancer</topic><topic>Adrenal Cortex Neoplasms - physiopathology</topic><topic>adrenocortical carcinoma</topic><topic>Adrenocorticotropic Hormone - metabolism</topic><topic>Cyclic AMP - metabolism</topic><topic>Cyclic AMP-Dependent Protein Kinases - metabolism</topic><topic>EGF</topic><topic>G proteins</topic><topic>Genes, ras - genetics</topic><topic>growth factors</topic><topic>Humans</topic><topic>insulin-like growth factor</topic><topic>Insulin-Like Growth Factor I - metabolism</topic><topic>Insulin-Like Growth Factor II - metabolism</topic><topic>mitogen-activated protein kinase (MAPK)</topic><topic>p53</topic><topic>protein kinase A (PKA)</topic><topic>ras</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>signal transduction</topic><topic>Signal Transduction - physiology</topic><topic>Transcription Factors - metabolism</topic><topic>Tumor Suppressor Protein p53 - genetics</topic><topic>Tumor Suppressor Protein p53 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KIRSCHNER, LAWRENCE S.</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>Annals of the New York Academy of Sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KIRSCHNER, LAWRENCE S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Signaling Pathways in Adrenocortical Cancer</atitle><jtitle>Annals of the New York Academy of Sciences</jtitle><addtitle>Ann N Y Acad Sci</addtitle><date>2002-06</date><risdate>2002</risdate><volume>968</volume><issue>1</issue><spage>222</spage><epage>239</epage><pages>222-239</pages><issn>0077-8923</issn><eissn>1749-6632</eissn><abstract>: Adrenocortical carcinoma is a rare tumor that carries a very poor prognosis. Despite efforts to develop new therapeutic regimens to treat this disease, surgery remains the mainstay of treatment. Laboratory studies of adrenocortical cancers have revealed a wide variety of signaling pathways that can be altered in these neoplasms. Although ACTH signaling through adenylyl cyclase and protein kinase A is important for normal adrenal cellular physiology, there is evidence to suggest that this pathway may inhibit the growth of adrenocortical tumors, and that inactivation of the ACTH receptor may promote tumor formation. Although multiple signal transduction pathways are essential for normal adrenal growth and hormone secretion, efforts to identify events required for neoplastic transformation have met with limited success. Alterations that have frequently been observed in adrenocortical carcinoma include up‐regulation of the IGF‐II system, as well as mutations in TP53 and RAS. Current studies aim to elucidate the mechanisms of tumor growth by studying proproliferative signaling pathways, such as those involving Akt/PKB and the mitogen‐activated protein kinases (MAPKs). Although studies of single pathways have been helpful in guiding investigations, new tools to study the integration and multiplicity of signaling pathways hold the hope of improved understanding of the signaling pathway alterations in adrenocortical cancer.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>12119279</pmid><doi>10.1111/j.1749-6632.2002.tb04338.x</doi><tpages>18</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0077-8923 |
ispartof | Annals of the New York Academy of Sciences, 2002-06, Vol.968 (1), p.222-239 |
issn | 0077-8923 1749-6632 |
language | eng |
recordid | cdi_proquest_miscellaneous_71909108 |
source | MEDLINE; Wiley Online Library Journals Frontfile Complete |
subjects | ACTH receptor adrenal cancer Adrenal Cortex Neoplasms - physiopathology adrenocortical carcinoma Adrenocorticotropic Hormone - metabolism Cyclic AMP - metabolism Cyclic AMP-Dependent Protein Kinases - metabolism EGF G proteins Genes, ras - genetics growth factors Humans insulin-like growth factor Insulin-Like Growth Factor I - metabolism Insulin-Like Growth Factor II - metabolism mitogen-activated protein kinase (MAPK) p53 protein kinase A (PKA) ras Receptors, Cell Surface - metabolism signal transduction Signal Transduction - physiology Transcription Factors - metabolism Tumor Suppressor Protein p53 - genetics Tumor Suppressor Protein p53 - metabolism |
title | Signaling Pathways in Adrenocortical Cancer |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T12%3A51%3A39IST&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=Signaling%20Pathways%20in%20Adrenocortical%20Cancer&rft.jtitle=Annals%20of%20the%20New%20York%20Academy%20of%20Sciences&rft.au=KIRSCHNER,%20LAWRENCE%20S.&rft.date=2002-06&rft.volume=968&rft.issue=1&rft.spage=222&rft.epage=239&rft.pages=222-239&rft.issn=0077-8923&rft.eissn=1749-6632&rft_id=info:doi/10.1111/j.1749-6632.2002.tb04338.x&rft_dat=%3Cproquest_cross%3E71909108%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=71909108&rft_id=info:pmid/12119279&rfr_iscdi=true |