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Galectin-7 Expression Potentiates HER-2-Positive Phenotype in Breast Cancer
HER-2 positive tumors are among the most aggressive subtypes of breast cancer and are frequently associated with metastasis and poor outcome. As with other aggressive subtypes of breast cancer, these tumors are associated with abnormally high expression of galectin-7 (gal-7), which confers metastati...
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Published in: | PloS one 2016-11, Vol.11 (11), p.e0166731-e0166731 |
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description | HER-2 positive tumors are among the most aggressive subtypes of breast cancer and are frequently associated with metastasis and poor outcome. As with other aggressive subtypes of breast cancer, these tumors are associated with abnormally high expression of galectin-7 (gal-7), which confers metastatic breast tumor cells with increased invasive behavior. Although previous studies in the rat model of breast tumorigenesis have shown that gal-7 is also increased in primary breast tumor, its contribution to the development of the primary breast tumors remains unclear. In the present work, we have used genetically-engineered gal-7-deficient mice to examine the role of gal-7 in the development of the mammary gland and of breast cancer. Using histological and immunohistological analysis of whole mammary glands at different stages of development, we detected no significant changes between normal and gal-7-deficient mice. To test the involvement of gal-7 in breast cancer, we next examined the effects of loss of gal-7 on mammary tumor development by crossing gal-7-deficient mice with the mammary tumor transgenic mouse strain FVB-Tg(MMTV-Erbb2)NK1Mul/J. Finally, assessment of mice survival and tumor volume showed a delay of mammary tumor growth in the absence of systemic gal-7. These data suggest that gal-7 could potentiate the phenotype of HER-2 positive primary breast cancer. |
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As with other aggressive subtypes of breast cancer, these tumors are associated with abnormally high expression of galectin-7 (gal-7), which confers metastatic breast tumor cells with increased invasive behavior. Although previous studies in the rat model of breast tumorigenesis have shown that gal-7 is also increased in primary breast tumor, its contribution to the development of the primary breast tumors remains unclear. In the present work, we have used genetically-engineered gal-7-deficient mice to examine the role of gal-7 in the development of the mammary gland and of breast cancer. Using histological and immunohistological analysis of whole mammary glands at different stages of development, we detected no significant changes between normal and gal-7-deficient mice. To test the involvement of gal-7 in breast cancer, we next examined the effects of loss of gal-7 on mammary tumor development by crossing gal-7-deficient mice with the mammary tumor transgenic mouse strain FVB-Tg(MMTV-Erbb2)NK1Mul/J. Finally, assessment of mice survival and tumor volume showed a delay of mammary tumor growth in the absence of systemic gal-7. These data suggest that gal-7 could potentiate the phenotype of HER-2 positive primary breast cancer.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0166731</identifier><identifier>PMID: 27902734</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Biology and Life Sciences ; Breast cancer ; Cancer ; Care and treatment ; Cell Line, Tumor ; Cell Proliferation - genetics ; Cell Transformation, Neoplastic - genetics ; Cellular Biology ; Change detection ; Development and progression ; Disease ; Disease Models, Animal ; Disease Progression ; ErbB-2 protein ; Female ; Galectins - genetics ; Gene amplification ; Gene expression ; Genetic aspects ; Genetic engineering ; Glands ; Health aspects ; Humans ; Invasiveness ; Lectins ; Life Sciences ; Longevity - genetics ; Mammary gland ; Mammary glands ; Mammary Glands, Animal - metabolism ; Mammary Neoplasms, Animal - mortality ; Mammary Neoplasms, Animal - pathology ; Mammary Tumor Virus, Mouse ; MCF-7 Cells ; Medicine and Health Sciences ; Metastases ; Metastasis ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Phenotypes ; Receptor, ErbB-2 - metabolism ; Research and Analysis Methods ; Rodents ; Transgenic animals ; Transgenic mice ; Tumor cells ; Tumorigenesis ; Tumors</subject><ispartof>PloS one, 2016-11, Vol.11 (11), p.e0166731-e0166731</ispartof><rights>COPYRIGHT 2016 Public Library of Science</rights><rights>2016 Grosset et al. 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To test the involvement of gal-7 in breast cancer, we next examined the effects of loss of gal-7 on mammary tumor development by crossing gal-7-deficient mice with the mammary tumor transgenic mouse strain FVB-Tg(MMTV-Erbb2)NK1Mul/J. Finally, assessment of mice survival and tumor volume showed a delay of mammary tumor growth in the absence of systemic gal-7. 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Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grosset, Andrée-Anne</au><au>Poirier, Françoise</au><au>Gaboury, Louis</au><au>St-Pierre, Yves</au><au>Samant, Rajeev</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Galectin-7 Expression Potentiates HER-2-Positive Phenotype in Breast Cancer</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2016-11-30</date><risdate>2016</risdate><volume>11</volume><issue>11</issue><spage>e0166731</spage><epage>e0166731</epage><pages>e0166731-e0166731</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>HER-2 positive tumors are among the most aggressive subtypes of breast cancer and are frequently associated with metastasis and poor outcome. As with other aggressive subtypes of breast cancer, these tumors are associated with abnormally high expression of galectin-7 (gal-7), which confers metastatic breast tumor cells with increased invasive behavior. Although previous studies in the rat model of breast tumorigenesis have shown that gal-7 is also increased in primary breast tumor, its contribution to the development of the primary breast tumors remains unclear. In the present work, we have used genetically-engineered gal-7-deficient mice to examine the role of gal-7 in the development of the mammary gland and of breast cancer. Using histological and immunohistological analysis of whole mammary glands at different stages of development, we detected no significant changes between normal and gal-7-deficient mice. To test the involvement of gal-7 in breast cancer, we next examined the effects of loss of gal-7 on mammary tumor development by crossing gal-7-deficient mice with the mammary tumor transgenic mouse strain FVB-Tg(MMTV-Erbb2)NK1Mul/J. Finally, assessment of mice survival and tumor volume showed a delay of mammary tumor growth in the absence of systemic gal-7. These data suggest that gal-7 could potentiate the phenotype of HER-2 positive primary breast cancer.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>27902734</pmid><doi>10.1371/journal.pone.0166731</doi><tpages>e0166731</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biology and Life Sciences Breast cancer Cancer Care and treatment Cell Line, Tumor Cell Proliferation - genetics Cell Transformation, Neoplastic - genetics Cellular Biology Change detection Development and progression Disease Disease Models, Animal Disease Progression ErbB-2 protein Female Galectins - genetics Gene amplification Gene expression Genetic aspects Genetic engineering Glands Health aspects Humans Invasiveness Lectins Life Sciences Longevity - genetics Mammary gland Mammary glands Mammary Glands, Animal - metabolism Mammary Neoplasms, Animal - mortality Mammary Neoplasms, Animal - pathology Mammary Tumor Virus, Mouse MCF-7 Cells Medicine and Health Sciences Metastases Metastasis Mice Mice, Inbred C57BL Mice, Knockout Phenotypes Receptor, ErbB-2 - metabolism Research and Analysis Methods Rodents Transgenic animals Transgenic mice Tumor cells Tumorigenesis Tumors |
title | Galectin-7 Expression Potentiates HER-2-Positive Phenotype in Breast Cancer |
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