Immunohistochemical evidence of NF-kB activation in canine lymphomas, histiocytic sarcomas, hemangiosarcomas, and mast cell tumors
Increased or constitutive activation of nuclear factor kappa B (NF-kB) is a feature of many chronic disease processes, including cancer. While NF-kB overactivation has been documented extensively in human oncology, there is a relative paucity of data documenting the same phenomenon in veterinary med...
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Veröffentlicht in: | Veterinary pathology 2024-01, Vol.61 (1), p.20-31 |
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description | Increased or constitutive activation of nuclear factor kappa B (NF-kB) is a feature of many chronic disease processes, including cancer. While NF-kB overactivation has been documented extensively in human oncology, there is a relative paucity of data documenting the same phenomenon in veterinary medicine. To assess NF-kB activity, antibodies to p65 and p100/p52, which are components of NF-kB heterodimers, were first validated for specificity and canine cross-reactivity via Western blot and labeling of immortalized cell pellets. Then, nuclear labeling for these antibodies was assessed via QuPath software in over 200 tumor tissue samples (10 hemangiosarcomas, 94 histiocytic sarcomas, 71 lymphomas, and 28 mast cell tumors) and compared to immunolabeling in appropriate normal tissue counterparts. Greater than 70% of spontaneous canine tumors evaluated in this study had more nuclear p65 and p100/p52 immunoreactivity than was observed in comparable normal cell populations. Specifically, 144/204 (70.58%) of tumors evaluated had positive p65 nuclear labeling and 179/195 (91.79%) had positive p100/p52 nuclear labeling. Surprisingly, greater nuclear p100/p52 reactivity was associated with a longer progression-free survival (PFS) and overall survival (OS) in canine lymphomas. These results provide support and preliminary data to investigate the role of NF-kB signaling in different types of canine cancer. |
doi_str_mv | 10.1177/03009858231180484 |
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Surprisingly, greater nuclear p100/p52 reactivity was associated with a longer progression-free survival (PFS) and overall survival (OS) in canine lymphomas. These results provide support and preliminary data to investigate the role of NF-kB signaling in different types of canine cancer.</description><identifier>ISSN: 0300-9858</identifier><identifier>EISSN: 1544-2217</identifier><identifier>DOI: 10.1177/03009858231180484</identifier><identifier>PMID: 37357953</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Animals ; Dog Diseases ; Dogs ; Hemangiosarcoma - veterinary ; Histiocytic Sarcoma - veterinary ; Humans ; Lymphoma - veterinary ; Mast Cells ; NF-kappa B - metabolism ; NF-kappa B p52 Subunit - metabolism</subject><ispartof>Veterinary pathology, 2024-01, Vol.61 (1), p.20-31</ispartof><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c292t-81d09ce3eafb2ffb03e792f7b61b107143f7eb679187f8d7dfc78bd3155ee023</cites><orcidid>0000-0001-6117-0909</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/03009858231180484$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/03009858231180484$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37357953$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schlein, Lisa J.</creatorcontrib><creatorcontrib>Thamm, Douglas H.</creatorcontrib><title>Immunohistochemical evidence of NF-kB activation in canine lymphomas, histiocytic sarcomas, hemangiosarcomas, and mast cell tumors</title><title>Veterinary pathology</title><addtitle>Vet Pathol</addtitle><description>Increased or constitutive activation of nuclear factor kappa B (NF-kB) is a feature of many chronic disease processes, including cancer. While NF-kB overactivation has been documented extensively in human oncology, there is a relative paucity of data documenting the same phenomenon in veterinary medicine. To assess NF-kB activity, antibodies to p65 and p100/p52, which are components of NF-kB heterodimers, were first validated for specificity and canine cross-reactivity via Western blot and labeling of immortalized cell pellets. Then, nuclear labeling for these antibodies was assessed via QuPath software in over 200 tumor tissue samples (10 hemangiosarcomas, 94 histiocytic sarcomas, 71 lymphomas, and 28 mast cell tumors) and compared to immunolabeling in appropriate normal tissue counterparts. Greater than 70% of spontaneous canine tumors evaluated in this study had more nuclear p65 and p100/p52 immunoreactivity than was observed in comparable normal cell populations. Specifically, 144/204 (70.58%) of tumors evaluated had positive p65 nuclear labeling and 179/195 (91.79%) had positive p100/p52 nuclear labeling. Surprisingly, greater nuclear p100/p52 reactivity was associated with a longer progression-free survival (PFS) and overall survival (OS) in canine lymphomas. These results provide support and preliminary data to investigate the role of NF-kB signaling in different types of canine cancer.</description><subject>Animals</subject><subject>Dog Diseases</subject><subject>Dogs</subject><subject>Hemangiosarcoma - veterinary</subject><subject>Histiocytic Sarcoma - veterinary</subject><subject>Humans</subject><subject>Lymphoma - veterinary</subject><subject>Mast Cells</subject><subject>NF-kappa B - metabolism</subject><subject>NF-kappa B p52 Subunit - metabolism</subject><issn>0300-9858</issn><issn>1544-2217</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EouXxAWyQlywI-JHU9hIQj0oVbNhHjjOmhtgucYLULV9OohZYILGa0cy5VzMXoRNKLigV4pJwQpQsJOOUSpLLfAdNaZHnGWNU7KLpuM9GYIIOUnolhDElxT6acMELoQo-RZ9z7_sQly510SzBO6MbDB-uhmAAR4sf77K3a6xN5z5052LALmCjgwuAm7VfLaPX6RyPehfNunMGJ92a7RS8Di8u_k50qPHQdNhA0-Cu97FNR2jP6ibB8bYeoue72-ebh2zxdD-_uVpkhinWZZLWRBngoG3FrK0IB6GYFdWMVpQImnMroJoJRaWwsha1NUJWNadFAUAYP0RnG9tVG997SF3pXRrP0AFin0ommRKkUCofULpBTRtTasGWq9Z53a5LSsox-fJP8oPmdGvfVx7qH8V31ANwsQGSfoHyNfZtGL79x_ELl0GN6A</recordid><startdate>202401</startdate><enddate>202401</enddate><creator>Schlein, Lisa J.</creator><creator>Thamm, Douglas H.</creator><general>SAGE Publications</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>7X8</scope><orcidid>https://orcid.org/0000-0001-6117-0909</orcidid></search><sort><creationdate>202401</creationdate><title>Immunohistochemical evidence of NF-kB activation in canine lymphomas, histiocytic sarcomas, hemangiosarcomas, and mast cell tumors</title><author>Schlein, Lisa J. ; Thamm, Douglas H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c292t-81d09ce3eafb2ffb03e792f7b61b107143f7eb679187f8d7dfc78bd3155ee023</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Dog Diseases</topic><topic>Dogs</topic><topic>Hemangiosarcoma - veterinary</topic><topic>Histiocytic Sarcoma - veterinary</topic><topic>Humans</topic><topic>Lymphoma - veterinary</topic><topic>Mast Cells</topic><topic>NF-kappa B - metabolism</topic><topic>NF-kappa B p52 Subunit - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schlein, Lisa J.</creatorcontrib><creatorcontrib>Thamm, Douglas H.</creatorcontrib><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>Veterinary pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schlein, Lisa J.</au><au>Thamm, Douglas H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunohistochemical evidence of NF-kB activation in canine lymphomas, histiocytic sarcomas, hemangiosarcomas, and mast cell tumors</atitle><jtitle>Veterinary pathology</jtitle><addtitle>Vet Pathol</addtitle><date>2024-01</date><risdate>2024</risdate><volume>61</volume><issue>1</issue><spage>20</spage><epage>31</epage><pages>20-31</pages><issn>0300-9858</issn><eissn>1544-2217</eissn><abstract>Increased or constitutive activation of nuclear factor kappa B (NF-kB) is a feature of many chronic disease processes, including cancer. While NF-kB overactivation has been documented extensively in human oncology, there is a relative paucity of data documenting the same phenomenon in veterinary medicine. To assess NF-kB activity, antibodies to p65 and p100/p52, which are components of NF-kB heterodimers, were first validated for specificity and canine cross-reactivity via Western blot and labeling of immortalized cell pellets. Then, nuclear labeling for these antibodies was assessed via QuPath software in over 200 tumor tissue samples (10 hemangiosarcomas, 94 histiocytic sarcomas, 71 lymphomas, and 28 mast cell tumors) and compared to immunolabeling in appropriate normal tissue counterparts. Greater than 70% of spontaneous canine tumors evaluated in this study had more nuclear p65 and p100/p52 immunoreactivity than was observed in comparable normal cell populations. Specifically, 144/204 (70.58%) of tumors evaluated had positive p65 nuclear labeling and 179/195 (91.79%) had positive p100/p52 nuclear labeling. 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subjects | Animals Dog Diseases Dogs Hemangiosarcoma - veterinary Histiocytic Sarcoma - veterinary Humans Lymphoma - veterinary Mast Cells NF-kappa B - metabolism NF-kappa B p52 Subunit - metabolism |
title | Immunohistochemical evidence of NF-kB activation in canine lymphomas, histiocytic sarcomas, hemangiosarcomas, and mast cell tumors |
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