Cooperativity between the polyamine pathway and HER‐2neu in transformation of human mammary epithelial cells in culture: Role of the MAPK pathway
Our experiments were designed to test the cooperativity between the polyamine pathway and HER‐2neu in inducing transformation of human mammary epithelial cells in culture. Using the MCF‐10A breast epithelial cell line, we observed that induction of overexpression of ornithine decarboxylase (ODC) (th...
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description | Our experiments were designed to test the cooperativity between the polyamine pathway and HER‐2neu in inducing transformation of human mammary epithelial cells in culture. Using the MCF‐10A breast epithelial cell line, we observed that induction of overexpression of ornithine decarboxylase (ODC) (the first rate‐limiting enzyme in polyamine biosynthesis) markedly potentiated the anchorage‐independent growth stimulating effect of the β2 isoform of neu differentiating factor (NDF) known to activate HER‐2neu in MCF‐10A cells. ODC overexpression, on the other hand, did not enhance growth in liquid culture, thus pointing to a specific effect on transformation rather than proliferation. ODC‐overexpressing MCF‐10A cells exhibited increased MAPK phosphorylation in response to administration of NDF and/or epidermal growth factor (EGF). In contrast, the phosphorylation of the members of the stress‐activated protein kinase cascade p38 and SEK were not affected by ODC overexpression. Of note, in the absence of EGF and NDF, ODC overexpression failed to induce both clonogenicity and MAPK activation. These results suggest that increased polyamine biosynthetic activity critically interacts with HER‐2neu in promoting human mammary cell transformation in culture and that the MAPK cascade is an important mediator of this interaction. If confirmed in future in vivo studies, our results may identify important new targets for the chemoprevention of human breast cancer. Int. J. Cancer 76:563–570, 1998.© 1998 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1097-0215(19980518)76:4<563::AID-IJC20>3.0.CO;2-7 |
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Using the MCF‐10A breast epithelial cell line, we observed that induction of overexpression of ornithine decarboxylase (ODC) (the first rate‐limiting enzyme in polyamine biosynthesis) markedly potentiated the anchorage‐independent growth stimulating effect of the β2 isoform of neu differentiating factor (NDF) known to activate HER‐2neu in MCF‐10A cells. ODC overexpression, on the other hand, did not enhance growth in liquid culture, thus pointing to a specific effect on transformation rather than proliferation. ODC‐overexpressing MCF‐10A cells exhibited increased MAPK phosphorylation in response to administration of NDF and/or epidermal growth factor (EGF). In contrast, the phosphorylation of the members of the stress‐activated protein kinase cascade p38 and SEK were not affected by ODC overexpression. Of note, in the absence of EGF and NDF, ODC overexpression failed to induce both clonogenicity and MAPK activation. These results suggest that increased polyamine biosynthetic activity critically interacts with HER‐2neu in promoting human mammary cell transformation in culture and that the MAPK cascade is an important mediator of this interaction. If confirmed in future in vivo studies, our results may identify important new targets for the chemoprevention of human breast cancer. Int. J. Cancer 76:563–570, 1998.© 1998 Wiley‐Liss, Inc.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/(SICI)1097-0215(19980518)76:4<563::AID-IJC20>3.0.CO;2-7</identifier><identifier>PMID: 9590135</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; Breast - metabolism ; Breast - pathology ; Breast Neoplasms - enzymology ; Breast Neoplasms - etiology ; Cell Line ; Cell Transformation, Neoplastic ; Clone Cells ; Enzyme Activation ; Epithelium ; ErbB Receptors - metabolism ; Gynecology. Andrology. 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Using the MCF‐10A breast epithelial cell line, we observed that induction of overexpression of ornithine decarboxylase (ODC) (the first rate‐limiting enzyme in polyamine biosynthesis) markedly potentiated the anchorage‐independent growth stimulating effect of the β2 isoform of neu differentiating factor (NDF) known to activate HER‐2neu in MCF‐10A cells. ODC overexpression, on the other hand, did not enhance growth in liquid culture, thus pointing to a specific effect on transformation rather than proliferation. ODC‐overexpressing MCF‐10A cells exhibited increased MAPK phosphorylation in response to administration of NDF and/or epidermal growth factor (EGF). In contrast, the phosphorylation of the members of the stress‐activated protein kinase cascade p38 and SEK were not affected by ODC overexpression. Of note, in the absence of EGF and NDF, ODC overexpression failed to induce both clonogenicity and MAPK activation. These results suggest that increased polyamine biosynthetic activity critically interacts with HER‐2neu in promoting human mammary cell transformation in culture and that the MAPK cascade is an important mediator of this interaction. If confirmed in future in vivo studies, our results may identify important new targets for the chemoprevention of human breast cancer. Int. J. Cancer 76:563–570, 1998.© 1998 Wiley‐Liss, Inc.</description><subject>Biological and medical sciences</subject><subject>Breast - metabolism</subject><subject>Breast - pathology</subject><subject>Breast Neoplasms - enzymology</subject><subject>Breast Neoplasms - etiology</subject><subject>Cell Line</subject><subject>Cell Transformation, Neoplastic</subject><subject>Clone Cells</subject><subject>Enzyme Activation</subject><subject>Epithelium</subject><subject>ErbB Receptors - metabolism</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Mammary gland diseases</subject><subject>MAP Kinase Kinase 1</subject><subject>Medical sciences</subject><subject>Mitogen-Activated Protein Kinase Kinases</subject><subject>Ornithine Decarboxylase - metabolism</subject><subject>Polyamines - metabolism</subject><subject>Protein-Serine-Threonine Kinases - metabolism</subject><subject>Protein-Tyrosine Kinases - metabolism</subject><subject>Receptor, ErbB-2 - metabolism</subject><subject>Signal Transduction</subject><subject>Tumors</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc-O0zAQxi0EWkrhEZB8QGj3kDK2kzguCFSFhS0sKlpAcBs5qa0G5U-JE6rceAQk3pAnwaHdXkDak0eeb775ND9CXjCYMQD-5PTDMl2eMVAyAM6iU6ZUAhFLzmQ8D59FsZjPF8uXwfJNyuG5mMEsXT3lgbxFJseZ22TinSCQTMR3yT3nvgIwFkF4Qk5UpICJaEJ-pU2zNa3uiu9FN9DMdDtjatptDN025aCrovaV7jY7PVBdr-nF-dXvHz95bXpaeF2ra2ebtvIGTU0bSzd9pWta6arS7UDNtvBWZaFLmpuydONM3pdd35o5vWpKM46My94t3r-93nOf3LG6dObB4Z2ST6_OP6YXweXq9TJdXAZ5BDEEuWBxFmVSaZBWh9Jom4CKRRZKCVZGljGd8IhDrCzkEBrLk8zmgq9DnfFciSl5vPfdts233rgOq8KNMXVtmt6hVIlU_mI3ClkcMpH4g07J570wbxvnWmNx2xbjIZABjlwRR644MsKREV5zRRljiJ4roueKf7miQMB0hRyld354iNBnlVkffQ8gff_Roa9drkvrueSFO8o45wwS8LIve9muKM3wT7obw_0v2_5D_AEWuczD</recordid><startdate>19980518</startdate><enddate>19980518</enddate><creator>Manni, Andrea</creator><creator>Wechter, Rita</creator><creator>Verderame, Michael F.</creator><creator>Mauger, David</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</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>7TO</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19980518</creationdate><title>Cooperativity between the polyamine pathway and HER‐2neu in transformation of human mammary epithelial cells in culture: Role of the MAPK pathway</title><author>Manni, Andrea ; Wechter, Rita ; Verderame, Michael F. ; Mauger, David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5060-c316b5b79a07fa47eaf80963b4770f75f11a8252069f0c04ef28bfc32d4ab2c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Biological and medical sciences</topic><topic>Breast - metabolism</topic><topic>Breast - pathology</topic><topic>Breast Neoplasms - enzymology</topic><topic>Breast Neoplasms - etiology</topic><topic>Cell Line</topic><topic>Cell Transformation, Neoplastic</topic><topic>Clone Cells</topic><topic>Enzyme Activation</topic><topic>Epithelium</topic><topic>ErbB Receptors - metabolism</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Mammary gland diseases</topic><topic>MAP Kinase Kinase 1</topic><topic>Medical sciences</topic><topic>Mitogen-Activated Protein Kinase Kinases</topic><topic>Ornithine Decarboxylase - metabolism</topic><topic>Polyamines - metabolism</topic><topic>Protein-Serine-Threonine Kinases - metabolism</topic><topic>Protein-Tyrosine Kinases - metabolism</topic><topic>Receptor, ErbB-2 - metabolism</topic><topic>Signal Transduction</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Manni, Andrea</creatorcontrib><creatorcontrib>Wechter, Rita</creatorcontrib><creatorcontrib>Verderame, Michael F.</creatorcontrib><creatorcontrib>Mauger, David</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>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Manni, Andrea</au><au>Wechter, Rita</au><au>Verderame, Michael F.</au><au>Mauger, David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cooperativity between the polyamine pathway and HER‐2neu in transformation of human mammary epithelial cells in culture: Role of the MAPK pathway</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>1998-05-18</date><risdate>1998</risdate><volume>76</volume><issue>4</issue><spage>563</spage><epage>570</epage><pages>563-570</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>Our experiments were designed to test the cooperativity between the polyamine pathway and HER‐2neu in inducing transformation of human mammary epithelial cells in culture. Using the MCF‐10A breast epithelial cell line, we observed that induction of overexpression of ornithine decarboxylase (ODC) (the first rate‐limiting enzyme in polyamine biosynthesis) markedly potentiated the anchorage‐independent growth stimulating effect of the β2 isoform of neu differentiating factor (NDF) known to activate HER‐2neu in MCF‐10A cells. ODC overexpression, on the other hand, did not enhance growth in liquid culture, thus pointing to a specific effect on transformation rather than proliferation. ODC‐overexpressing MCF‐10A cells exhibited increased MAPK phosphorylation in response to administration of NDF and/or epidermal growth factor (EGF). In contrast, the phosphorylation of the members of the stress‐activated protein kinase cascade p38 and SEK were not affected by ODC overexpression. Of note, in the absence of EGF and NDF, ODC overexpression failed to induce both clonogenicity and MAPK activation. These results suggest that increased polyamine biosynthetic activity critically interacts with HER‐2neu in promoting human mammary cell transformation in culture and that the MAPK cascade is an important mediator of this interaction. If confirmed in future in vivo studies, our results may identify important new targets for the chemoprevention of human breast cancer. Int. J. Cancer 76:563–570, 1998.© 1998 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>9590135</pmid><doi>10.1002/(SICI)1097-0215(19980518)76:4<563::AID-IJC20>3.0.CO;2-7</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences Breast - metabolism Breast - pathology Breast Neoplasms - enzymology Breast Neoplasms - etiology Cell Line Cell Transformation, Neoplastic Clone Cells Enzyme Activation Epithelium ErbB Receptors - metabolism Gynecology. Andrology. Obstetrics Humans Mammary gland diseases MAP Kinase Kinase 1 Medical sciences Mitogen-Activated Protein Kinase Kinases Ornithine Decarboxylase - metabolism Polyamines - metabolism Protein-Serine-Threonine Kinases - metabolism Protein-Tyrosine Kinases - metabolism Receptor, ErbB-2 - metabolism Signal Transduction Tumors |
title | Cooperativity between the polyamine pathway and HER‐2neu in transformation of human mammary epithelial cells in culture: Role of the MAPK pathway |
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