Anti-insulin-like growth factor strategies in breast cancer
The insulin-like growth factors (IGF-I and -II) are potent mitogens and survival factors for both normal and malignant breast cells. These effects are mediated primarily through the IGF-I receptor (IGF-IR), which is significantly overexpressed and highly activated in breast tumors. The IGF-binding p...
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Veröffentlicht in: | Seminars in oncology 2004-02, Vol.31 (1 Suppl 3), p.54-63 |
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creator | Jerome, Lori Shiry, Laura Leyland-Jones, Brian |
description | The insulin-like growth factors (IGF-I and -II) are potent mitogens and survival factors for both normal and malignant breast cells. These effects are mediated primarily through the IGF-I receptor (IGF-IR), which is significantly overexpressed and highly activated in breast tumors. The IGF-binding proteins are competitive inhibitors of IGF/IGF-IR interaction, limiting cellular proliferation and survival. Higher serum IGF-I levels or an increased ratio of IGF-I to IGF binding protein-3 is associated with an increased risk of developing breast cancer. Hence, interest in the IGF system as a potential target for the development of novel antineoplastic therapies has ensued. Several strategies to interrupt IGF-IR signaling are currently being evaluated for the treatment of breast cancer, including suppression of IGF production, reduction of functional IGF-IR levels, neutralization of IGF action, and inhibition of IGF-IR activation. |
doi_str_mv | 10.1053/j.seminoncol.2004.01.007 |
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These effects are mediated primarily through the IGF-I receptor (IGF-IR), which is significantly overexpressed and highly activated in breast tumors. The IGF-binding proteins are competitive inhibitors of IGF/IGF-IR interaction, limiting cellular proliferation and survival. Higher serum IGF-I levels or an increased ratio of IGF-I to IGF binding protein-3 is associated with an increased risk of developing breast cancer. Hence, interest in the IGF system as a potential target for the development of novel antineoplastic therapies has ensued. 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Several strategies to interrupt IGF-IR signaling are currently being evaluated for the treatment of breast cancer, including suppression of IGF production, reduction of functional IGF-IR levels, neutralization of IGF action, and inhibition of IGF-IR activation.</description><subject>Animals</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - metabolism</subject><subject>Humans</subject><subject>Receptors, Somatomedin - antagonists & inhibitors</subject><subject>Receptors, Somatomedin - metabolism</subject><subject>Signal Transduction - drug effects</subject><issn>0093-7754</issn><issn>1532-8708</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1OwzAQhC0EoqXwCignxCVh7dixLU6l4k-qxAXOVuJsikuaFNsF8fakaiVu9LSH_WZGmiEkoZBREPnNMgu4cl3f2b7NGADPgGYA8oiMqchZqiSoYzIG0HkqpeAjchbCEoBRydgpGVEBggmej8nttIsudV3YtK5LW_eBycL33_E9aUobe5-E6MuIC4chcV1SeSxDTGzZWfTn5KQp24AX-zshbw_3r7OndP7y-DybzlPLcx5TnlPV6JzWVqAqAGxTFTVjAmhJGbM1KqsqrZkqlNLIeQ2aCamHr66agvN8Qq52vmvff24wRLNywWLblh32m2AklUpDIQbw-l-QKikULwb4oCeVRaGBbsPVDrS-D8FjY9berUr_YyiY7Rhmaf7GMNsxDFAzjDFIL_cZm2qF9Z9w3_4A3O0AHNr7cuhNsA6Hamvn0UZT9-5wyi8fqp56</recordid><startdate>20040201</startdate><enddate>20040201</enddate><creator>Jerome, Lori</creator><creator>Shiry, Laura</creator><creator>Leyland-Jones, Brian</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>7TO</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20040201</creationdate><title>Anti-insulin-like growth factor strategies in breast cancer</title><author>Jerome, Lori ; Shiry, Laura ; Leyland-Jones, Brian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-4318f931dc5e8600cfb6d22501a122cde8c8b99286889e44d0925791a19bf6443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - metabolism</topic><topic>Humans</topic><topic>Receptors, Somatomedin - antagonists & inhibitors</topic><topic>Receptors, Somatomedin - metabolism</topic><topic>Signal Transduction - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jerome, Lori</creatorcontrib><creatorcontrib>Shiry, Laura</creatorcontrib><creatorcontrib>Leyland-Jones, Brian</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Seminars in oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jerome, Lori</au><au>Shiry, Laura</au><au>Leyland-Jones, Brian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anti-insulin-like growth factor strategies in breast cancer</atitle><jtitle>Seminars in oncology</jtitle><addtitle>Semin Oncol</addtitle><date>2004-02-01</date><risdate>2004</risdate><volume>31</volume><issue>1 Suppl 3</issue><spage>54</spage><epage>63</epage><pages>54-63</pages><issn>0093-7754</issn><eissn>1532-8708</eissn><abstract>The insulin-like growth factors (IGF-I and -II) are potent mitogens and survival factors for both normal and malignant breast cells. 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subjects | Animals Antineoplastic Agents - pharmacology Breast Neoplasms - drug therapy Breast Neoplasms - metabolism Humans Receptors, Somatomedin - antagonists & inhibitors Receptors, Somatomedin - metabolism Signal Transduction - drug effects |
title | Anti-insulin-like growth factor strategies in breast cancer |
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