Piper nigrum extract suppresses tumor growth and enhances the antitumor immune response in murine models of breast cancer and melanoma

Although the antitumor effect of P. nigrum has been widely studied, research related to its possible immunomodulatory effects is relatively scarce. Here, the antitumor and immunomodulatory activity of an ethanolic extract of P. nigrum were evaluated in the murine models of 4T1 breast cancer and B16-...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cancer Immunology, Immunotherapy Immunotherapy, 2023-10, Vol.72 (10), p.3279-3292
Hauptverfasser: Lasso, Paola, Rojas, Laura, Arévalo, Cindy, Urueña, Claudia, Murillo, Natalia, Nossa, Paula, Sandoval, Tito, Chitiva, Luis Carlos, Barreto, Alfonso, Costa, Geison M., Fiorentino, Susana
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 3292
container_issue 10
container_start_page 3279
container_title Cancer Immunology, Immunotherapy
container_volume 72
creator Lasso, Paola
Rojas, Laura
Arévalo, Cindy
Urueña, Claudia
Murillo, Natalia
Nossa, Paula
Sandoval, Tito
Chitiva, Luis Carlos
Barreto, Alfonso
Costa, Geison M.
Fiorentino, Susana
description Although the antitumor effect of P. nigrum has been widely studied, research related to its possible immunomodulatory effects is relatively scarce. Here, the antitumor and immunomodulatory activity of an ethanolic extract of P. nigrum were evaluated in the murine models of 4T1 breast cancer and B16-F10 melanoma. In vitro evaluations showed that the P. nigrum extract has cytotoxic activity, induces apoptotic cell death, and has a pro-oxidant effect in both cell lines, but it regulates glucose uptake differently in both lines, decreasing it in 4T1 but not in B16-F10. P. nigrum extract significantly reduced tumor size in both models and decreased the occurrence of macrometastases in 4T1 model. Evaluation of immune subpopulations by flow cytometry revealed that the P. nigrum extract significantly increases the frequency of dendritic cells and activated CD8 + T cells and decreases the frequency of myeloid-derived suppressor like cells and Tregs in the tumor microenvironment of both models but with different dynamics. Our findings strongly suggest that the P. nigrum extract exerts immunomodulatory functions, slightly related to the modulation of cellular energy metabolism, which could ultimately contribute to the promising antitumor effect of P. nigrum .
doi_str_mv 10.1007/s00262-023-03487-3
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10491708</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2839739772</sourcerecordid><originalsourceid>FETCH-LOGICAL-c475t-37a3254d6c3d2a8131691e6e714994beeaed544d22f52fefe780d188223d401d3</originalsourceid><addsrcrecordid>eNp9kc1u1DAUhS1ERYfCC7BAlth0E-q_xM4KoYo_qVJZwNryxDczrmI72HGBF-hz42lKoSyQLMU697vHOToIvaDkNSVEnmVCWMcawnhDuFCy4Y_QhgpeJdXSx2hTVdJIQsQxeprzVb0w0vdP0DGXohO0Zxt089nNkHBwu1Q8hh9LMsOCc5nnBDlDxkvxMeFdit-XPTbBYgh7E4bDZA9VWNxKOO9LAFy35hgyYBewL8lVyUcLU8ZxxNsEJi94OOynWzMPkwnRm2foaDRThud33xP09f27L-cfm4vLD5_O3140g5Dt0nBpOGuF7QZumVGU066n0IGkou_FFsCAbYWwjI0tG2EEqYilSjHGrSDU8hP0ZvWdy9aDHSDUwJOek_Mm_dTROP1wEtxe7-K1pkT0VBJVHU7vHFL8ViAv2rs8wFRzQCxZM8V7WY9kFX31D3oVSwo1X6U61nWEqwPFVmpIMecE4_3fUKIPPeu1Z1171rc9a16XXv6d437ld7EV4CuQ6yjsIP15-z-2vwBOHrZa</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2862660382</pqid></control><display><type>article</type><title>Piper nigrum extract suppresses tumor growth and enhances the antitumor immune response in murine models of breast cancer and melanoma</title><source>Springer Nature - Complete Springer Journals</source><source>PubMed Central</source><creator>Lasso, Paola ; Rojas, Laura ; Arévalo, Cindy ; Urueña, Claudia ; Murillo, Natalia ; Nossa, Paula ; Sandoval, Tito ; Chitiva, Luis Carlos ; Barreto, Alfonso ; Costa, Geison M. ; Fiorentino, Susana</creator><creatorcontrib>Lasso, Paola ; Rojas, Laura ; Arévalo, Cindy ; Urueña, Claudia ; Murillo, Natalia ; Nossa, Paula ; Sandoval, Tito ; Chitiva, Luis Carlos ; Barreto, Alfonso ; Costa, Geison M. ; Fiorentino, Susana</creatorcontrib><description>Although the antitumor effect of P. nigrum has been widely studied, research related to its possible immunomodulatory effects is relatively scarce. Here, the antitumor and immunomodulatory activity of an ethanolic extract of P. nigrum were evaluated in the murine models of 4T1 breast cancer and B16-F10 melanoma. In vitro evaluations showed that the P. nigrum extract has cytotoxic activity, induces apoptotic cell death, and has a pro-oxidant effect in both cell lines, but it regulates glucose uptake differently in both lines, decreasing it in 4T1 but not in B16-F10. P. nigrum extract significantly reduced tumor size in both models and decreased the occurrence of macrometastases in 4T1 model. Evaluation of immune subpopulations by flow cytometry revealed that the P. nigrum extract significantly increases the frequency of dendritic cells and activated CD8 + T cells and decreases the frequency of myeloid-derived suppressor like cells and Tregs in the tumor microenvironment of both models but with different dynamics. Our findings strongly suggest that the P. nigrum extract exerts immunomodulatory functions, slightly related to the modulation of cellular energy metabolism, which could ultimately contribute to the promising antitumor effect of P. nigrum .</description><identifier>ISSN: 0340-7004</identifier><identifier>EISSN: 1432-0851</identifier><identifier>DOI: 10.1007/s00262-023-03487-3</identifier><identifier>PMID: 37464192</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animal models ; Antitumor activity ; Apoptosis ; Breast cancer ; Cancer Research ; CD8 antigen ; Cell death ; Cytotoxicity ; Dendritic cells ; Energy metabolism ; Flow cytometry ; Immunology ; Immunomodulation ; Lymphocytes T ; Medicine ; Medicine &amp; Public Health ; Melanoma ; Oncology ; Oxidants ; Tumor microenvironment ; Tumors</subject><ispartof>Cancer Immunology, Immunotherapy, 2023-10, Vol.72 (10), p.3279-3292</ispartof><rights>The Author(s) 2023</rights><rights>2023. The Author(s).</rights><rights>The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c475t-37a3254d6c3d2a8131691e6e714994beeaed544d22f52fefe780d188223d401d3</citedby><cites>FETCH-LOGICAL-c475t-37a3254d6c3d2a8131691e6e714994beeaed544d22f52fefe780d188223d401d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491708/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10491708/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37464192$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lasso, Paola</creatorcontrib><creatorcontrib>Rojas, Laura</creatorcontrib><creatorcontrib>Arévalo, Cindy</creatorcontrib><creatorcontrib>Urueña, Claudia</creatorcontrib><creatorcontrib>Murillo, Natalia</creatorcontrib><creatorcontrib>Nossa, Paula</creatorcontrib><creatorcontrib>Sandoval, Tito</creatorcontrib><creatorcontrib>Chitiva, Luis Carlos</creatorcontrib><creatorcontrib>Barreto, Alfonso</creatorcontrib><creatorcontrib>Costa, Geison M.</creatorcontrib><creatorcontrib>Fiorentino, Susana</creatorcontrib><title>Piper nigrum extract suppresses tumor growth and enhances the antitumor immune response in murine models of breast cancer and melanoma</title><title>Cancer Immunology, Immunotherapy</title><addtitle>Cancer Immunol Immunother</addtitle><addtitle>Cancer Immunol Immunother</addtitle><description>Although the antitumor effect of P. nigrum has been widely studied, research related to its possible immunomodulatory effects is relatively scarce. Here, the antitumor and immunomodulatory activity of an ethanolic extract of P. nigrum were evaluated in the murine models of 4T1 breast cancer and B16-F10 melanoma. In vitro evaluations showed that the P. nigrum extract has cytotoxic activity, induces apoptotic cell death, and has a pro-oxidant effect in both cell lines, but it regulates glucose uptake differently in both lines, decreasing it in 4T1 but not in B16-F10. P. nigrum extract significantly reduced tumor size in both models and decreased the occurrence of macrometastases in 4T1 model. Evaluation of immune subpopulations by flow cytometry revealed that the P. nigrum extract significantly increases the frequency of dendritic cells and activated CD8 + T cells and decreases the frequency of myeloid-derived suppressor like cells and Tregs in the tumor microenvironment of both models but with different dynamics. Our findings strongly suggest that the P. nigrum extract exerts immunomodulatory functions, slightly related to the modulation of cellular energy metabolism, which could ultimately contribute to the promising antitumor effect of P. nigrum .</description><subject>Animal models</subject><subject>Antitumor activity</subject><subject>Apoptosis</subject><subject>Breast cancer</subject><subject>Cancer Research</subject><subject>CD8 antigen</subject><subject>Cell death</subject><subject>Cytotoxicity</subject><subject>Dendritic cells</subject><subject>Energy metabolism</subject><subject>Flow cytometry</subject><subject>Immunology</subject><subject>Immunomodulation</subject><subject>Lymphocytes T</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Melanoma</subject><subject>Oncology</subject><subject>Oxidants</subject><subject>Tumor microenvironment</subject><subject>Tumors</subject><issn>0340-7004</issn><issn>1432-0851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kc1u1DAUhS1ERYfCC7BAlth0E-q_xM4KoYo_qVJZwNryxDczrmI72HGBF-hz42lKoSyQLMU697vHOToIvaDkNSVEnmVCWMcawnhDuFCy4Y_QhgpeJdXSx2hTVdJIQsQxeprzVb0w0vdP0DGXohO0Zxt089nNkHBwu1Q8hh9LMsOCc5nnBDlDxkvxMeFdit-XPTbBYgh7E4bDZA9VWNxKOO9LAFy35hgyYBewL8lVyUcLU8ZxxNsEJi94OOynWzMPkwnRm2foaDRThud33xP09f27L-cfm4vLD5_O3140g5Dt0nBpOGuF7QZumVGU066n0IGkou_FFsCAbYWwjI0tG2EEqYilSjHGrSDU8hP0ZvWdy9aDHSDUwJOek_Mm_dTROP1wEtxe7-K1pkT0VBJVHU7vHFL8ViAv2rs8wFRzQCxZM8V7WY9kFX31D3oVSwo1X6U61nWEqwPFVmpIMecE4_3fUKIPPeu1Z1171rc9a16XXv6d437ld7EV4CuQ6yjsIP15-z-2vwBOHrZa</recordid><startdate>20231001</startdate><enddate>20231001</enddate><creator>Lasso, Paola</creator><creator>Rojas, Laura</creator><creator>Arévalo, Cindy</creator><creator>Urueña, Claudia</creator><creator>Murillo, Natalia</creator><creator>Nossa, Paula</creator><creator>Sandoval, Tito</creator><creator>Chitiva, Luis Carlos</creator><creator>Barreto, Alfonso</creator><creator>Costa, Geison M.</creator><creator>Fiorentino, Susana</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20231001</creationdate><title>Piper nigrum extract suppresses tumor growth and enhances the antitumor immune response in murine models of breast cancer and melanoma</title><author>Lasso, Paola ; Rojas, Laura ; Arévalo, Cindy ; Urueña, Claudia ; Murillo, Natalia ; Nossa, Paula ; Sandoval, Tito ; Chitiva, Luis Carlos ; Barreto, Alfonso ; Costa, Geison M. ; Fiorentino, Susana</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c475t-37a3254d6c3d2a8131691e6e714994beeaed544d22f52fefe780d188223d401d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Animal models</topic><topic>Antitumor activity</topic><topic>Apoptosis</topic><topic>Breast cancer</topic><topic>Cancer Research</topic><topic>CD8 antigen</topic><topic>Cell death</topic><topic>Cytotoxicity</topic><topic>Dendritic cells</topic><topic>Energy metabolism</topic><topic>Flow cytometry</topic><topic>Immunology</topic><topic>Immunomodulation</topic><topic>Lymphocytes T</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Melanoma</topic><topic>Oncology</topic><topic>Oxidants</topic><topic>Tumor microenvironment</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lasso, Paola</creatorcontrib><creatorcontrib>Rojas, Laura</creatorcontrib><creatorcontrib>Arévalo, Cindy</creatorcontrib><creatorcontrib>Urueña, Claudia</creatorcontrib><creatorcontrib>Murillo, Natalia</creatorcontrib><creatorcontrib>Nossa, Paula</creatorcontrib><creatorcontrib>Sandoval, Tito</creatorcontrib><creatorcontrib>Chitiva, Luis Carlos</creatorcontrib><creatorcontrib>Barreto, Alfonso</creatorcontrib><creatorcontrib>Costa, Geison M.</creatorcontrib><creatorcontrib>Fiorentino, Susana</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</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>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science 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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer Immunology, Immunotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lasso, Paola</au><au>Rojas, Laura</au><au>Arévalo, Cindy</au><au>Urueña, Claudia</au><au>Murillo, Natalia</au><au>Nossa, Paula</au><au>Sandoval, Tito</au><au>Chitiva, Luis Carlos</au><au>Barreto, Alfonso</au><au>Costa, Geison M.</au><au>Fiorentino, Susana</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Piper nigrum extract suppresses tumor growth and enhances the antitumor immune response in murine models of breast cancer and melanoma</atitle><jtitle>Cancer Immunology, Immunotherapy</jtitle><stitle>Cancer Immunol Immunother</stitle><addtitle>Cancer Immunol Immunother</addtitle><date>2023-10-01</date><risdate>2023</risdate><volume>72</volume><issue>10</issue><spage>3279</spage><epage>3292</epage><pages>3279-3292</pages><issn>0340-7004</issn><eissn>1432-0851</eissn><abstract>Although the antitumor effect of P. nigrum has been widely studied, research related to its possible immunomodulatory effects is relatively scarce. Here, the antitumor and immunomodulatory activity of an ethanolic extract of P. nigrum were evaluated in the murine models of 4T1 breast cancer and B16-F10 melanoma. In vitro evaluations showed that the P. nigrum extract has cytotoxic activity, induces apoptotic cell death, and has a pro-oxidant effect in both cell lines, but it regulates glucose uptake differently in both lines, decreasing it in 4T1 but not in B16-F10. P. nigrum extract significantly reduced tumor size in both models and decreased the occurrence of macrometastases in 4T1 model. Evaluation of immune subpopulations by flow cytometry revealed that the P. nigrum extract significantly increases the frequency of dendritic cells and activated CD8 + T cells and decreases the frequency of myeloid-derived suppressor like cells and Tregs in the tumor microenvironment of both models but with different dynamics. Our findings strongly suggest that the P. nigrum extract exerts immunomodulatory functions, slightly related to the modulation of cellular energy metabolism, which could ultimately contribute to the promising antitumor effect of P. nigrum .</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>37464192</pmid><doi>10.1007/s00262-023-03487-3</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0340-7004
ispartof Cancer Immunology, Immunotherapy, 2023-10, Vol.72 (10), p.3279-3292
issn 0340-7004
1432-0851
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10491708
source Springer Nature - Complete Springer Journals; PubMed Central
subjects Animal models
Antitumor activity
Apoptosis
Breast cancer
Cancer Research
CD8 antigen
Cell death
Cytotoxicity
Dendritic cells
Energy metabolism
Flow cytometry
Immunology
Immunomodulation
Lymphocytes T
Medicine
Medicine & Public Health
Melanoma
Oncology
Oxidants
Tumor microenvironment
Tumors
title Piper nigrum extract suppresses tumor growth and enhances the antitumor immune response in murine models of breast cancer and melanoma
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T09%3A59%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Piper%20nigrum%20extract%20suppresses%20tumor%20growth%20and%20enhances%20the%20antitumor%20immune%20response%20in%20murine%20models%20of%20breast%20cancer%20and%20melanoma&rft.jtitle=Cancer%20Immunology,%20Immunotherapy&rft.au=Lasso,%20Paola&rft.date=2023-10-01&rft.volume=72&rft.issue=10&rft.spage=3279&rft.epage=3292&rft.pages=3279-3292&rft.issn=0340-7004&rft.eissn=1432-0851&rft_id=info:doi/10.1007/s00262-023-03487-3&rft_dat=%3Cproquest_pubme%3E2839739772%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2862660382&rft_id=info:pmid/37464192&rfr_iscdi=true