S100A10 Has a Critical Regulatory Function in Mammary Tumor Growth and Metastasis: Insights Using MMTV-PyMT Oncomice and Clinical Patient Sample Analysis

S100A10 (p11) is a plasminogen receptor that regulates cellular plasmin generation by cancer cells. In the current study, we used the MMTV-PyMT mouse breast cancer model, patient tumor microarray, and immunohistochemical (IHC) analysis to investigate the role of p11 in oncogenesis. The genetic delet...

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Veröffentlicht in:Cancers 2020-12, Vol.12 (12), p.3673
Hauptverfasser: Bharadwaj, Alamelu G, Dahn, Margaret L, Liu, Rong-Zong, Colp, Patricia, Thomas, Lynn N, Holloway, Ryan W, Marignani, Paola A, Too, Catherine Kl, Barnes, Penelope J, Godbout, Rosaline, Marcato, Paola, Waisman, David M
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container_issue 12
container_start_page 3673
container_title Cancers
container_volume 12
creator Bharadwaj, Alamelu G
Dahn, Margaret L
Liu, Rong-Zong
Colp, Patricia
Thomas, Lynn N
Holloway, Ryan W
Marignani, Paola A
Too, Catherine Kl
Barnes, Penelope J
Godbout, Rosaline
Marcato, Paola
Waisman, David M
description S100A10 (p11) is a plasminogen receptor that regulates cellular plasmin generation by cancer cells. In the current study, we used the MMTV-PyMT mouse breast cancer model, patient tumor microarray, and immunohistochemical (IHC) analysis to investigate the role of p11 in oncogenesis. The genetic deletion of p11 resulted in significantly decreased tumor onset, growth rate, and spontaneous pulmonary metastatic burden in the PyMT/p11-KO (knock-out) mice. This phenotype was accompanied by substantial reduction in Ki67 positivity, macrophage infiltration, decreased vascular density in the primary tumors, and decrease in invasive carcinoma and pulmonary metastasis. Surprisingly, IHC analysis of wild-type MMTV-PyMT mice failed to detect p11 expression in the tumors or metastatic tumor cells and loss of p11 did not decrease plasmin generation in the PyMT tumors and cells. Furthermore, tumor cells expressing p11 displayed dramatically reduced lung metastasis when injected into p11-depleted mice, further strengthening the stromal role of p11 in tumor growth and metastasis. Transcriptome analysis of the PyMT tumors from p11-KO mice showed marked reduction in genes such as , , and involved in breast cancer development, progression, and inflammation. The PyMT/p11-KO tumors displayed a remarkable increase in inflammatory cytokines such as interleukin ( , , and interferon ( )- . Gene expression profiling and IHC of primary breast cancer samples showed that p11 mRNA and protein levels were significantly higher in tumor tissues compared to normal mammary tissue. P11 mRNA expression was significantly associated with poor patient prognosis and significantly elevated in high grade, triple negative (TN) tumors, and tumors with high proliferative index. This is the first study examining the crucial role of p11 in breast tumor development and metastasis, thus emphasizing its potential as a diagnostic and prognostic biomarker in breast cancer.
doi_str_mv 10.3390/cancers12123673
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In the current study, we used the MMTV-PyMT mouse breast cancer model, patient tumor microarray, and immunohistochemical (IHC) analysis to investigate the role of p11 in oncogenesis. The genetic deletion of p11 resulted in significantly decreased tumor onset, growth rate, and spontaneous pulmonary metastatic burden in the PyMT/p11-KO (knock-out) mice. This phenotype was accompanied by substantial reduction in Ki67 positivity, macrophage infiltration, decreased vascular density in the primary tumors, and decrease in invasive carcinoma and pulmonary metastasis. Surprisingly, IHC analysis of wild-type MMTV-PyMT mice failed to detect p11 expression in the tumors or metastatic tumor cells and loss of p11 did not decrease plasmin generation in the PyMT tumors and cells. Furthermore, tumor cells expressing p11 displayed dramatically reduced lung metastasis when injected into p11-depleted mice, further strengthening the stromal role of p11 in tumor growth and metastasis. Transcriptome analysis of the PyMT tumors from p11-KO mice showed marked reduction in genes such as , , and involved in breast cancer development, progression, and inflammation. The PyMT/p11-KO tumors displayed a remarkable increase in inflammatory cytokines such as interleukin ( , , and interferon ( )- . Gene expression profiling and IHC of primary breast cancer samples showed that p11 mRNA and protein levels were significantly higher in tumor tissues compared to normal mammary tissue. P11 mRNA expression was significantly associated with poor patient prognosis and significantly elevated in high grade, triple negative (TN) tumors, and tumors with high proliferative index. 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Dahn, Margaret L ; Liu, Rong-Zong ; Colp, Patricia ; Thomas, Lynn N ; Holloway, Ryan W ; Marignani, Paola A ; Too, Catherine Kl ; Barnes, Penelope J ; Godbout, Rosaline ; Marcato, Paola ; Waisman, David M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-a6dffd79309a8a3b856a6f96d2d6613daf51121f68ba055cb06b7aebb4734a4b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Age</topic><topic>Breast cancer</topic><topic>Calcium-binding protein</topic><topic>Cell growth</topic><topic>DNA microarrays</topic><topic>Fibrosarcoma</topic><topic>Gene expression</topic><topic>Growth rate</topic><topic>Inflammation</topic><topic>Interferon</topic><topic>Interleukin 10</topic><topic>Invasiveness</topic><topic>Lung carcinoma</topic><topic>Lungs</topic><topic>Macrophages</topic><topic>Mammary gland</topic><topic>Medical prognosis</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Phenotypes</topic><topic>Plasmin</topic><topic>Rodents</topic><topic>S100 protein</topic><topic>Tumor cells</topic><topic>Tumorigenesis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bharadwaj, Alamelu G</creatorcontrib><creatorcontrib>Dahn, Margaret L</creatorcontrib><creatorcontrib>Liu, Rong-Zong</creatorcontrib><creatorcontrib>Colp, Patricia</creatorcontrib><creatorcontrib>Thomas, Lynn N</creatorcontrib><creatorcontrib>Holloway, Ryan W</creatorcontrib><creatorcontrib>Marignani, Paola A</creatorcontrib><creatorcontrib>Too, Catherine Kl</creatorcontrib><creatorcontrib>Barnes, Penelope J</creatorcontrib><creatorcontrib>Godbout, Rosaline</creatorcontrib><creatorcontrib>Marcato, Paola</creatorcontrib><creatorcontrib>Waisman, David M</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bharadwaj, Alamelu G</au><au>Dahn, Margaret L</au><au>Liu, Rong-Zong</au><au>Colp, Patricia</au><au>Thomas, Lynn N</au><au>Holloway, Ryan W</au><au>Marignani, Paola A</au><au>Too, Catherine Kl</au><au>Barnes, Penelope J</au><au>Godbout, Rosaline</au><au>Marcato, Paola</au><au>Waisman, David M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>S100A10 Has a Critical Regulatory Function in Mammary Tumor Growth and Metastasis: Insights Using MMTV-PyMT Oncomice and Clinical Patient Sample Analysis</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2020-12-07</date><risdate>2020</risdate><volume>12</volume><issue>12</issue><spage>3673</spage><pages>3673-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>S100A10 (p11) is a plasminogen receptor that regulates cellular plasmin generation by cancer cells. In the current study, we used the MMTV-PyMT mouse breast cancer model, patient tumor microarray, and immunohistochemical (IHC) analysis to investigate the role of p11 in oncogenesis. The genetic deletion of p11 resulted in significantly decreased tumor onset, growth rate, and spontaneous pulmonary metastatic burden in the PyMT/p11-KO (knock-out) mice. This phenotype was accompanied by substantial reduction in Ki67 positivity, macrophage infiltration, decreased vascular density in the primary tumors, and decrease in invasive carcinoma and pulmonary metastasis. Surprisingly, IHC analysis of wild-type MMTV-PyMT mice failed to detect p11 expression in the tumors or metastatic tumor cells and loss of p11 did not decrease plasmin generation in the PyMT tumors and cells. Furthermore, tumor cells expressing p11 displayed dramatically reduced lung metastasis when injected into p11-depleted mice, further strengthening the stromal role of p11 in tumor growth and metastasis. Transcriptome analysis of the PyMT tumors from p11-KO mice showed marked reduction in genes such as , , and involved in breast cancer development, progression, and inflammation. The PyMT/p11-KO tumors displayed a remarkable increase in inflammatory cytokines such as interleukin ( , , and interferon ( )- . Gene expression profiling and IHC of primary breast cancer samples showed that p11 mRNA and protein levels were significantly higher in tumor tissues compared to normal mammary tissue. P11 mRNA expression was significantly associated with poor patient prognosis and significantly elevated in high grade, triple negative (TN) tumors, and tumors with high proliferative index. 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subjects Age
Breast cancer
Calcium-binding protein
Cell growth
DNA microarrays
Fibrosarcoma
Gene expression
Growth rate
Inflammation
Interferon
Interleukin 10
Invasiveness
Lung carcinoma
Lungs
Macrophages
Mammary gland
Medical prognosis
Metastases
Metastasis
Phenotypes
Plasmin
Rodents
S100 protein
Tumor cells
Tumorigenesis
Tumors
title S100A10 Has a Critical Regulatory Function in Mammary Tumor Growth and Metastasis: Insights Using MMTV-PyMT Oncomice and Clinical Patient Sample Analysis
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