Inflammasome activation, NLRP3 engagement and macrophage recruitment to tumor microenvironment are all required for Salmonella antitumor effect
Salmonella -based cancer therapies show great potential in preclinical models, but for most cases the observed antitumor effect is transient. Understanding the basis of the antitumor efficacy might guide the design of improved strains that elicit long-lasting effects, paving the wave for clinical us...
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description | Salmonella
-based cancer therapies show great potential in preclinical models, but for most cases the observed antitumor effect is transient. Understanding the basis of the antitumor efficacy might guide the design of improved strains that elicit long-lasting effects, paving the wave for clinical use. Here, we deepened into the role of macrophages and inflammasome activation in the context of
Salmonella
anti-melanoma effect. We showed inflammasome activation in melanoma cells upon infection, which correlated with cell surface exposure of gasdermin-D (GSDM-D) and calreticulin (CRT) and High mobility group box 1 protein (HMGB-1) release, suggesting immunogenic cell death, particularly pyroptosis.
Salmonella
infection upregulated levels of
Caspase-11
(
Casp11
) mRNA, but not
Nlrp3
or
Nlrc4
mRNA, the only described inflammasome receptors engaged by
Salmonella
, suggesting that non-canonical inflammasome activation could be occurring in melanoma cells. Intratumoral administration of
Salmonella
to melanoma-bearing mice elicited local inflammasome activation and interleukin-1β (IL-1β) production together with tumor growth retardation and extended survival in wild type but not
Caspase-1/11
(
Casp1/11
) knockout mice despite similar levels of intratumoral IL-1β in the later.
Salmonella
antitumor activity was also suppressed in melanoma bearing
Nlrp3
knockout mice.
Salmonella
induced macrophage recruitment to the tumor site and infiltrating cells exhibited inflammasome activation. Depletion experiments confirmed that macrophages are also essential for
Salmonella
anti-melanoma effect. Intratumoral macrophages showed a marked M2/M1 shift soon after treatment but this inflammatory profile is then lost, which could explain the transient effect of therapy. All in all, our results highlight CASP-1/11 axis and macrophages as essential players in
Salmonella
-based cancer immunotherapy and suggest a possible target for future interventions. |
doi_str_mv | 10.1007/s00262-022-03148-x |
format | Article |
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-based cancer therapies show great potential in preclinical models, but for most cases the observed antitumor effect is transient. Understanding the basis of the antitumor efficacy might guide the design of improved strains that elicit long-lasting effects, paving the wave for clinical use. Here, we deepened into the role of macrophages and inflammasome activation in the context of
Salmonella
anti-melanoma effect. We showed inflammasome activation in melanoma cells upon infection, which correlated with cell surface exposure of gasdermin-D (GSDM-D) and calreticulin (CRT) and High mobility group box 1 protein (HMGB-1) release, suggesting immunogenic cell death, particularly pyroptosis.
Salmonella
infection upregulated levels of
Caspase-11
(
Casp11
) mRNA, but not
Nlrp3
or
Nlrc4
mRNA, the only described inflammasome receptors engaged by
Salmonella
, suggesting that non-canonical inflammasome activation could be occurring in melanoma cells. Intratumoral administration of
Salmonella
to melanoma-bearing mice elicited local inflammasome activation and interleukin-1β (IL-1β) production together with tumor growth retardation and extended survival in wild type but not
Caspase-1/11
(
Casp1/11
) knockout mice despite similar levels of intratumoral IL-1β in the later.
Salmonella
antitumor activity was also suppressed in melanoma bearing
Nlrp3
knockout mice.
Salmonella
induced macrophage recruitment to the tumor site and infiltrating cells exhibited inflammasome activation. Depletion experiments confirmed that macrophages are also essential for
Salmonella
anti-melanoma effect. Intratumoral macrophages showed a marked M2/M1 shift soon after treatment but this inflammatory profile is then lost, which could explain the transient effect of therapy. All in all, our results highlight CASP-1/11 axis and macrophages as essential players in
Salmonella
-based cancer immunotherapy and suggest a possible target for future interventions.</description><identifier>ISSN: 0340-7004</identifier><identifier>EISSN: 1432-0851</identifier><identifier>DOI: 10.1007/s00262-022-03148-x</identifier><identifier>PMID: 35061085</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animals ; Antitumor activity ; Calreticulin ; Cancer immunotherapy ; Cancer Research ; Caspase 1 - metabolism ; Caspase-1 ; Caspase-11 ; Cell activation ; Cell death ; Cell surface ; Growth rate ; High mobility group proteins ; IL-1β ; Immunogenicity ; Immunology ; Immunotherapy ; Inflammasomes ; Inflammasomes - immunology ; Inflammation ; Interleukin-1beta - metabolism ; Macrophages ; Macrophages - immunology ; Medicine ; Medicine & Public Health ; Melanoma ; Mice ; Mice, Inbred C57BL ; mRNA ; Neoplasms - immunology ; Neoplasms - therapy ; NLR Family, Pyrin Domain-Containing 3 Protein - genetics ; Oncology ; Original ; Original Article ; Pyroptosis ; RNA, Messenger - metabolism ; Salmonella ; Tumor Microenvironment ; Tumor-infiltrating lymphocytes</subject><ispartof>Cancer Immunology, Immunotherapy, 2022-09, Vol.71 (9), p.2141-2150</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022</rights><rights>2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-f125c806263e862dc2de6a02eb1b58b422a954a7d24d1f5caa455553c309b2703</citedby><cites>FETCH-LOGICAL-c431t-f125c806263e862dc2de6a02eb1b58b422a954a7d24d1f5caa455553c309b2703</cites><orcidid>0000-0002-1759-228X ; 0000-0002-6006-0713 ; 0000-0002-5548-698X ; 0000-0002-7294-6693 ; 0000-0002-2052-4114</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10992890/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10992890/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,41488,42557,51319,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35061085$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mónaco, Amy</creatorcontrib><creatorcontrib>Chilibroste, Sofía</creatorcontrib><creatorcontrib>Yim, Lucía</creatorcontrib><creatorcontrib>Chabalgoity, Jose Alejandro</creatorcontrib><creatorcontrib>Moreno, María</creatorcontrib><title>Inflammasome activation, NLRP3 engagement and macrophage recruitment to tumor microenvironment are all required for Salmonella antitumor effect</title><title>Cancer Immunology, Immunotherapy</title><addtitle>Cancer Immunol Immunother</addtitle><addtitle>Cancer Immunol Immunother</addtitle><description>Salmonella
-based cancer therapies show great potential in preclinical models, but for most cases the observed antitumor effect is transient. Understanding the basis of the antitumor efficacy might guide the design of improved strains that elicit long-lasting effects, paving the wave for clinical use. Here, we deepened into the role of macrophages and inflammasome activation in the context of
Salmonella
anti-melanoma effect. We showed inflammasome activation in melanoma cells upon infection, which correlated with cell surface exposure of gasdermin-D (GSDM-D) and calreticulin (CRT) and High mobility group box 1 protein (HMGB-1) release, suggesting immunogenic cell death, particularly pyroptosis.
Salmonella
infection upregulated levels of
Caspase-11
(
Casp11
) mRNA, but not
Nlrp3
or
Nlrc4
mRNA, the only described inflammasome receptors engaged by
Salmonella
, suggesting that non-canonical inflammasome activation could be occurring in melanoma cells. Intratumoral administration of
Salmonella
to melanoma-bearing mice elicited local inflammasome activation and interleukin-1β (IL-1β) production together with tumor growth retardation and extended survival in wild type but not
Caspase-1/11
(
Casp1/11
) knockout mice despite similar levels of intratumoral IL-1β in the later.
Salmonella
antitumor activity was also suppressed in melanoma bearing
Nlrp3
knockout mice.
Salmonella
induced macrophage recruitment to the tumor site and infiltrating cells exhibited inflammasome activation. Depletion experiments confirmed that macrophages are also essential for
Salmonella
anti-melanoma effect. Intratumoral macrophages showed a marked M2/M1 shift soon after treatment but this inflammatory profile is then lost, which could explain the transient effect of therapy. All in all, our results highlight CASP-1/11 axis and macrophages as essential players in
Salmonella
-based cancer immunotherapy and suggest a possible target for future interventions.</description><subject>Animals</subject><subject>Antitumor activity</subject><subject>Calreticulin</subject><subject>Cancer immunotherapy</subject><subject>Cancer Research</subject><subject>Caspase 1 - metabolism</subject><subject>Caspase-1</subject><subject>Caspase-11</subject><subject>Cell activation</subject><subject>Cell death</subject><subject>Cell surface</subject><subject>Growth rate</subject><subject>High mobility group proteins</subject><subject>IL-1β</subject><subject>Immunogenicity</subject><subject>Immunology</subject><subject>Immunotherapy</subject><subject>Inflammasomes</subject><subject>Inflammasomes - immunology</subject><subject>Inflammation</subject><subject>Interleukin-1beta - metabolism</subject><subject>Macrophages</subject><subject>Macrophages - immunology</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Melanoma</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>mRNA</subject><subject>Neoplasms - immunology</subject><subject>Neoplasms - therapy</subject><subject>NLR Family, Pyrin Domain-Containing 3 Protein - genetics</subject><subject>Oncology</subject><subject>Original</subject><subject>Original Article</subject><subject>Pyroptosis</subject><subject>RNA, Messenger - metabolism</subject><subject>Salmonella</subject><subject>Tumor Microenvironment</subject><subject>Tumor-infiltrating lymphocytes</subject><issn>0340-7004</issn><issn>1432-0851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kcluFDEQhi1ERIbAC3BALXHhQAdvvZ0QigKJNALEcrbc7uqJo7Y9sd2j5Cl4ZWrSSVgOWLK81Fe_q_wT8oLRY0Zp8zZRymteUo5TMNmW14_IikmBx7Zij8mKCknLhlJ5SJ6mdIkbTrvuCTkUFa0ZQivy89yPk3ZOp-Cg0Cbbnc42-DfFp_XXL6IAv9EbcOBzof1QOG1i2F7gVRHBxNnm21AORZ5diIWzGAe_szH4JSmi6jQhfTXbCEMxIvVNTy54mCaNotkuqTCOYPIzcjDqKcHzu_WI_Phw-v3krFx__nh-8n5dGilYLkfGK9PSmtcC2poPhg9Qa8qhZ33V9pJz3VVSNwOXAxsro7WscAgjaNfzhooj8m7R3c69g8FgrVFPahut0_FGBW3V3xFvL9Qm7BTDH-Rtt1d4facQw9UMKStnk9k35SHMSaE1nDdSdDWir_5BL8McPfansBYmOOuaPcUXCr8wpQjjQzWMqr3hajFcoeHq1nB1jUkv_-zjIeXeYQTEAiQM-Q3E32__R_YXwFe6Gg</recordid><startdate>20220901</startdate><enddate>20220901</enddate><creator>Mónaco, Amy</creator><creator>Chilibroste, Sofía</creator><creator>Yim, Lucía</creator><creator>Chabalgoity, Jose Alejandro</creator><creator>Moreno, María</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</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>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>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1759-228X</orcidid><orcidid>https://orcid.org/0000-0002-6006-0713</orcidid><orcidid>https://orcid.org/0000-0002-5548-698X</orcidid><orcidid>https://orcid.org/0000-0002-7294-6693</orcidid><orcidid>https://orcid.org/0000-0002-2052-4114</orcidid></search><sort><creationdate>20220901</creationdate><title>Inflammasome activation, NLRP3 engagement and macrophage recruitment to tumor microenvironment are all required for Salmonella antitumor effect</title><author>Mónaco, Amy ; Chilibroste, Sofía ; Yim, Lucía ; Chabalgoity, Jose Alejandro ; Moreno, María</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-f125c806263e862dc2de6a02eb1b58b422a954a7d24d1f5caa455553c309b2703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Antitumor activity</topic><topic>Calreticulin</topic><topic>Cancer immunotherapy</topic><topic>Cancer Research</topic><topic>Caspase 1 - metabolism</topic><topic>Caspase-1</topic><topic>Caspase-11</topic><topic>Cell activation</topic><topic>Cell death</topic><topic>Cell surface</topic><topic>Growth rate</topic><topic>High mobility group proteins</topic><topic>IL-1β</topic><topic>Immunogenicity</topic><topic>Immunology</topic><topic>Immunotherapy</topic><topic>Inflammasomes</topic><topic>Inflammasomes - immunology</topic><topic>Inflammation</topic><topic>Interleukin-1beta - metabolism</topic><topic>Macrophages</topic><topic>Macrophages - immunology</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Melanoma</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>mRNA</topic><topic>Neoplasms - immunology</topic><topic>Neoplasms - therapy</topic><topic>NLR Family, Pyrin Domain-Containing 3 Protein - genetics</topic><topic>Oncology</topic><topic>Original</topic><topic>Original Article</topic><topic>Pyroptosis</topic><topic>RNA, Messenger - metabolism</topic><topic>Salmonella</topic><topic>Tumor Microenvironment</topic><topic>Tumor-infiltrating lymphocytes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mónaco, Amy</creatorcontrib><creatorcontrib>Chilibroste, Sofía</creatorcontrib><creatorcontrib>Yim, Lucía</creatorcontrib><creatorcontrib>Chabalgoity, Jose Alejandro</creatorcontrib><creatorcontrib>Moreno, María</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & 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 & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & 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>ProQuest Central China</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>Mónaco, Amy</au><au>Chilibroste, Sofía</au><au>Yim, Lucía</au><au>Chabalgoity, Jose Alejandro</au><au>Moreno, María</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inflammasome activation, NLRP3 engagement and macrophage recruitment to tumor microenvironment are all required for Salmonella antitumor effect</atitle><jtitle>Cancer Immunology, Immunotherapy</jtitle><stitle>Cancer Immunol Immunother</stitle><addtitle>Cancer Immunol Immunother</addtitle><date>2022-09-01</date><risdate>2022</risdate><volume>71</volume><issue>9</issue><spage>2141</spage><epage>2150</epage><pages>2141-2150</pages><issn>0340-7004</issn><eissn>1432-0851</eissn><abstract>Salmonella
-based cancer therapies show great potential in preclinical models, but for most cases the observed antitumor effect is transient. Understanding the basis of the antitumor efficacy might guide the design of improved strains that elicit long-lasting effects, paving the wave for clinical use. Here, we deepened into the role of macrophages and inflammasome activation in the context of
Salmonella
anti-melanoma effect. We showed inflammasome activation in melanoma cells upon infection, which correlated with cell surface exposure of gasdermin-D (GSDM-D) and calreticulin (CRT) and High mobility group box 1 protein (HMGB-1) release, suggesting immunogenic cell death, particularly pyroptosis.
Salmonella
infection upregulated levels of
Caspase-11
(
Casp11
) mRNA, but not
Nlrp3
or
Nlrc4
mRNA, the only described inflammasome receptors engaged by
Salmonella
, suggesting that non-canonical inflammasome activation could be occurring in melanoma cells. Intratumoral administration of
Salmonella
to melanoma-bearing mice elicited local inflammasome activation and interleukin-1β (IL-1β) production together with tumor growth retardation and extended survival in wild type but not
Caspase-1/11
(
Casp1/11
) knockout mice despite similar levels of intratumoral IL-1β in the later.
Salmonella
antitumor activity was also suppressed in melanoma bearing
Nlrp3
knockout mice.
Salmonella
induced macrophage recruitment to the tumor site and infiltrating cells exhibited inflammasome activation. Depletion experiments confirmed that macrophages are also essential for
Salmonella
anti-melanoma effect. Intratumoral macrophages showed a marked M2/M1 shift soon after treatment but this inflammatory profile is then lost, which could explain the transient effect of therapy. All in all, our results highlight CASP-1/11 axis and macrophages as essential players in
Salmonella
-based cancer immunotherapy and suggest a possible target for future interventions.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>35061085</pmid><doi>10.1007/s00262-022-03148-x</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-1759-228X</orcidid><orcidid>https://orcid.org/0000-0002-6006-0713</orcidid><orcidid>https://orcid.org/0000-0002-5548-698X</orcidid><orcidid>https://orcid.org/0000-0002-7294-6693</orcidid><orcidid>https://orcid.org/0000-0002-2052-4114</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; SpringerNature Journals; PubMed Central |
subjects | Animals Antitumor activity Calreticulin Cancer immunotherapy Cancer Research Caspase 1 - metabolism Caspase-1 Caspase-11 Cell activation Cell death Cell surface Growth rate High mobility group proteins IL-1β Immunogenicity Immunology Immunotherapy Inflammasomes Inflammasomes - immunology Inflammation Interleukin-1beta - metabolism Macrophages Macrophages - immunology Medicine Medicine & Public Health Melanoma Mice Mice, Inbred C57BL mRNA Neoplasms - immunology Neoplasms - therapy NLR Family, Pyrin Domain-Containing 3 Protein - genetics Oncology Original Original Article Pyroptosis RNA, Messenger - metabolism Salmonella Tumor Microenvironment Tumor-infiltrating lymphocytes |
title | Inflammasome activation, NLRP3 engagement and macrophage recruitment to tumor microenvironment are all required for Salmonella antitumor effect |
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