CLIC2 regulates immunosuppression and macrophage differentiation in genomically stable gastric cancer
Chloride intracellular channels (CLICs) are a family of six evolutionarily conserved proteins with diverse functions. Previously, we identified CLIC2, as the fifth-ranked master regulator associated with diffuse-type gastric cancer (dGC) showing increased expression in tumors. Here we used bulk, as...
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Published in | Biology direct Vol. 20; no. 1; pp. 89 - 16 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
22.07.2025
BioMed Central Ltd BMC |
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Online Access | Get full text |
ISSN | 1745-6150 1745-6150 |
DOI | 10.1186/s13062-025-00666-3 |
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Abstract | Chloride intracellular channels (CLICs) are a family of six evolutionarily conserved proteins with diverse functions. Previously, we identified CLIC2, as the fifth-ranked master regulator associated with diffuse-type gastric cancer (dGC) showing increased expression in tumors. Here we used bulk, as well as single cell sequencing datasets of dGC, to demonstrate for the first time a direct association of CLIC2 with the microsatellite stable GC and, furthermore, the expression of CLIC2 in macrophages (MCs), and endothelial cells (ECs) populating gastric tissue. We generated CLIC2 knock-out THP-1 monocytic cells (THP-1CLIC2_KO) determining that while CLIC2 deletion had no observable effect on monocytes, THP-1CLIC2_KO macrophages exhibited significant morphological changes, including increased membrane protrusions, and upregulated expression of CD11b, CD11c, CD80, and CD86 markers. Furthermore, cytokine secretion profiling of THP-1CLIC2_KO differentiated cells revealed elevated secretion of CCL8, alongside reduced secretion of IL-1β, IL-6, and osteoprotegerin (OPG). Additionally, we observed increased phosphorylation of Shp1 phosphatase with the concomitant absence of Stat3 phosphorylation, which impaired downstream signaling, in line with the evidence that Clic2 interacts with both Shp1 and Stat3. Based on these findings, we suggest that CLIC2 plays a pivotal role in regulating monocyte-to-macrophage differentiation by modulating the Stat3 signaling pathway, thus enhancing gastric cancer progression by establishing a tumor-permissive microenvironment. |
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AbstractList | Chloride intracellular channels (CLICs) are a family of six evolutionarily conserved proteins with diverse functions. Previously, we identified CLIC2, as the fifth-ranked master regulator associated with diffuse-type gastric cancer (dGC) showing increased expression in tumors. Here we used bulk, as well as single cell sequencing datasets of dGC, to demonstrate for the first time a direct association of CLIC2 with the microsatellite stable GC and, furthermore, the expression of CLIC2 in macrophages (MCs), and endothelial cells (ECs) populating gastric tissue. We generated CLIC2 knock-out THP-1 monocytic cells (THP-1CLIC2_KO) determining that while CLIC2 deletion had no observable effect on monocytes, THP-1CLIC2_KO macrophages exhibited significant morphological changes, including increased membrane protrusions, and upregulated expression of CD11b, CD11c, CD80, and CD86 markers. Furthermore, cytokine secretion profiling of THP-1CLIC2_KO differentiated cells revealed elevated secretion of CCL8, alongside reduced secretion of IL-1β, IL-6, and osteoprotegerin (OPG). Additionally, we observed increased phosphorylation of Shp1 phosphatase with the concomitant absence of Stat3 phosphorylation, which impaired downstream signaling, in line with the evidence that Clic2 interacts with both Shp1 and Stat3. Based on these findings, we suggest that CLIC2 plays a pivotal role in regulating monocyte-to-macrophage differentiation by modulating the Stat3 signaling pathway, thus enhancing gastric cancer progression by establishing a tumor-permissive microenvironment. Chloride intracellular channels (CLICs) are a family of six evolutionarily conserved proteins with diverse functions. Previously, we identified CLIC2, as the fifth-ranked master regulator associated with diffuse-type gastric cancer (dGC) showing increased expression in tumors. Here we used bulk, as well as single cell sequencing datasets of dGC, to demonstrate for the first time a direct association of CLIC2 with the microsatellite stable GC and, furthermore, the expression of CLIC2 in macrophages (MCs), and endothelial cells (ECs) populating gastric tissue. We generated CLIC2 knock-out THP-1 monocytic cells (THP-1CLIC2_KO) determining that while CLIC2 deletion had no observable effect on monocytes, THP-1CLIC2_KO macrophages exhibited significant morphological changes, including increased membrane protrusions, and upregulated expression of CD11b, CD11c, CD80, and CD86 markers. Furthermore, cytokine secretion profiling of THP-1CLIC2_KO differentiated cells revealed elevated secretion of CCL8, alongside reduced secretion of IL-1[beta], IL-6, and osteoprotegerin (OPG). Additionally, we observed increased phosphorylation of Shp1 phosphatase with the concomitant absence of Stat3 phosphorylation, which impaired downstream signaling, in line with the evidence that Clic2 interacts with both Shp1 and Stat3. Based on these findings, we suggest that CLIC2 plays a pivotal role in regulating monocyte-to-macrophage differentiation by modulating the Stat3 signaling pathway, thus enhancing gastric cancer progression by establishing a tumor-permissive microenvironment. Chloride intracellular channels (CLICs) are a family of six evolutionarily conserved proteins with diverse functions. Previously, we identified CLIC2, as the fifth-ranked master regulator associated with diffuse-type gastric cancer (dGC) showing increased expression in tumors. Here we used bulk, as well as single cell sequencing datasets of dGC, to demonstrate for the first time a direct association of CLIC2 with the microsatellite stable GC and, furthermore, the expression of CLIC2 in macrophages (MCs), and endothelial cells (ECs) populating gastric tissue. We generated CLIC2 knock-out THP-1 monocytic cells (THP-1CLIC2_KO) determining that while CLIC2 deletion had no observable effect on monocytes, THP-1CLIC2_KO macrophages exhibited significant morphological changes, including increased membrane protrusions, and upregulated expression of CD11b, CD11c, CD80, and CD86 markers. Furthermore, cytokine secretion profiling of THP-1CLIC2_KO differentiated cells revealed elevated secretion of CCL8, alongside reduced secretion of IL-1β, IL-6, and osteoprotegerin (OPG). Additionally, we observed increased phosphorylation of Shp1 phosphatase with the concomitant absence of Stat3 phosphorylation, which impaired downstream signaling, in line with the evidence that Clic2 interacts with both Shp1 and Stat3. Based on these findings, we suggest that CLIC2 plays a pivotal role in regulating monocyte-to-macrophage differentiation by modulating the Stat3 signaling pathway, thus enhancing gastric cancer progression by establishing a tumor-permissive microenvironment.Chloride intracellular channels (CLICs) are a family of six evolutionarily conserved proteins with diverse functions. Previously, we identified CLIC2, as the fifth-ranked master regulator associated with diffuse-type gastric cancer (dGC) showing increased expression in tumors. Here we used bulk, as well as single cell sequencing datasets of dGC, to demonstrate for the first time a direct association of CLIC2 with the microsatellite stable GC and, furthermore, the expression of CLIC2 in macrophages (MCs), and endothelial cells (ECs) populating gastric tissue. We generated CLIC2 knock-out THP-1 monocytic cells (THP-1CLIC2_KO) determining that while CLIC2 deletion had no observable effect on monocytes, THP-1CLIC2_KO macrophages exhibited significant morphological changes, including increased membrane protrusions, and upregulated expression of CD11b, CD11c, CD80, and CD86 markers. Furthermore, cytokine secretion profiling of THP-1CLIC2_KO differentiated cells revealed elevated secretion of CCL8, alongside reduced secretion of IL-1β, IL-6, and osteoprotegerin (OPG). Additionally, we observed increased phosphorylation of Shp1 phosphatase with the concomitant absence of Stat3 phosphorylation, which impaired downstream signaling, in line with the evidence that Clic2 interacts with both Shp1 and Stat3. Based on these findings, we suggest that CLIC2 plays a pivotal role in regulating monocyte-to-macrophage differentiation by modulating the Stat3 signaling pathway, thus enhancing gastric cancer progression by establishing a tumor-permissive microenvironment. Chloride intracellular channels (CLICs) are a family of six evolutionarily conserved proteins with diverse functions. Previously, we identified CLIC2, as the fifth-ranked master regulator associated with diffuse-type gastric cancer (dGC) showing increased expression in tumors. Here we used bulk, as well as single cell sequencing datasets of dGC, to demonstrate for the first time a direct association of CLIC2 with the microsatellite stable GC and, furthermore, the expression of CLIC2 in macrophages (MCs), and endothelial cells (ECs) populating gastric tissue. We generated CLIC2 knock-out THP-1 monocytic cells (THP-1CLIC2_KO) determining that while CLIC2 deletion had no observable effect on monocytes, THP-1CLIC2_KO macrophages exhibited significant morphological changes, including increased membrane protrusions, and upregulated expression of CD11b, CD11c, CD80, and CD86 markers. Furthermore, cytokine secretion profiling of THP-1CLIC2_KO differentiated cells revealed elevated secretion of CCL8, alongside reduced secretion of IL-1[beta], IL-6, and osteoprotegerin (OPG). Additionally, we observed increased phosphorylation of Shp1 phosphatase with the concomitant absence of Stat3 phosphorylation, which impaired downstream signaling, in line with the evidence that Clic2 interacts with both Shp1 and Stat3. Based on these findings, we suggest that CLIC2 plays a pivotal role in regulating monocyte-to-macrophage differentiation by modulating the Stat3 signaling pathway, thus enhancing gastric cancer progression by establishing a tumor-permissive microenvironment. Keywords: Gastric microenvironment, Tumor microenvironment, Gastric cancer, Clic2, Macrophages, Differentiation, Signaling Chloride intracellular channels (CLICs) are a family of six evolutionarily conserved proteins with diverse functions. Previously, we identified CLIC2, as the fifth-ranked master regulator associated with diffuse-type gastric cancer (dGC) showing increased expression in tumors. Here we used bulk, as well as single cell sequencing datasets of dGC, to demonstrate for the first time a direct association of CLIC2 with the microsatellite stable GC and, furthermore, the expression of CLIC2 in macrophages (MCs), and endothelial cells (ECs) populating gastric tissue. We generated CLIC2 knock-out THP-1 monocytic cells (THP-1CLIC2_KO) determining that while CLIC2 deletion had no observable effect on monocytes, THP-1CLIC2_KO macrophages exhibited significant morphological changes, including increased membrane protrusions, and upregulated expression of CD11b, CD11c, CD80, and CD86 markers. Furthermore, cytokine secretion profiling of THP-1CLIC2_KO differentiated cells revealed elevated secretion of CCL8, alongside reduced secretion of IL-1β, IL-6, and osteoprotegerin (OPG). Additionally, we observed increased phosphorylation of Shp1 phosphatase with the concomitant absence of Stat3 phosphorylation, which impaired downstream signaling, in line with the evidence that Clic2 interacts with both Shp1 and Stat3. Based on these findings, we suggest that CLIC2 plays a pivotal role in regulating monocyte-to-macrophage differentiation by modulating the Stat3 signaling pathway, thus enhancing gastric cancer progression by establishing a tumor-permissive microenvironment. Abstract Chloride intracellular channels (CLICs) are a family of six evolutionarily conserved proteins with diverse functions. Previously, we identified CLIC2, as the fifth-ranked master regulator associated with diffuse-type gastric cancer (dGC) showing increased expression in tumors. Here we used bulk, as well as single cell sequencing datasets of dGC, to demonstrate for the first time a direct association of CLIC2 with the microsatellite stable GC and, furthermore, the expression of CLIC2 in macrophages (MCs), and endothelial cells (ECs) populating gastric tissue. We generated CLIC2 knock-out THP-1 monocytic cells (THP-1CLIC2_KO) determining that while CLIC2 deletion had no observable effect on monocytes, THP-1CLIC2_KO macrophages exhibited significant morphological changes, including increased membrane protrusions, and upregulated expression of CD11b, CD11c, CD80, and CD86 markers. Furthermore, cytokine secretion profiling of THP-1CLIC2_KO differentiated cells revealed elevated secretion of CCL8, alongside reduced secretion of IL-1β, IL-6, and osteoprotegerin (OPG). Additionally, we observed increased phosphorylation of Shp1 phosphatase with the concomitant absence of Stat3 phosphorylation, which impaired downstream signaling, in line with the evidence that Clic2 interacts with both Shp1 and Stat3. Based on these findings, we suggest that CLIC2 plays a pivotal role in regulating monocyte-to-macrophage differentiation by modulating the Stat3 signaling pathway, thus enhancing gastric cancer progression by establishing a tumor-permissive microenvironment. |
ArticleNumber | 89 |
Audience | Academic |
Author | De Vita, Ferdinando Luongo, Margherita Sabato, Claudia Pagliara, Valentina Amodio, Giuseppina Russi, Sabino Milone, Maria Rita De Stefano, Cristofaro Balzamo, Chiara Remondelli, Paolo Di Paola, Giuseppina Calice, Giovanni Longo, Viviana Albano, Francesco Zoppoli, Pietro Patitucci, Giuseppe Lucci, Valeria Cesta, Giuseppe Falco, Geppino Notarangelo, Tiziana Guadagno, Roberta Laurino, Simona Mazzone, Pellegrino Amendola, Elena |
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Cites_doi | 10.1016/j.jim.2019.112721 10.1016/j.celrep.2019.04.052 10.1016/j.xcrm.2024.101621 10.1038/s41419-023-05876-z 10.1038/nature13480 10.1186/s12943-017-0606-y 10.1038/ng.3593 10.1016/j.bbamem.2014.12.012 10.1038/s41467-024-46301-z 10.1038/s41423-020-0412-0 10.1016/j.celrep.2023.113236 10.1080/21688370.2019.1593775 10.1016/j.febslet.2010.01.027 10.1093/nar/gkad841 10.3390/cancers16132370 10.1038/s41587-023-01767-y 10.1016/j.febslet.2010.03.013 10.1186/1471-2105-7-S1-S7 10.18632/aging.103712 10.7150/thno.22182 10.1016/j.semcancer.2022.11.010 10.1038/s41392-023-01452-1 10.3390/genes14061169 10.1186/1471-2199-15-21 10.1242/jcs.189795 10.1016/j.neo.2021.06.001 10.1038/ncomms3612 10.1038/s41568-021-00363-z 10.3390/ijms22179379 10.3390/cancers14194890 10.1038/s41419-017-0026-3 10.3390/ijms17111848 10.1038/nature08712 10.3390/ijms20194900 10.1111/apm.1965.64.1.31 10.1590/S1679-45082015RB3438 10.21037/tgh.2020.01.02 10.1158/2159-8290.CD-21-0683 10.1038/s41467-022-28803-w 10.1038/s41418-020-00662-2 10.3390/cancers14194961 |
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Keywords | Signaling Tumor microenvironment Gastric microenvironment Macrophages Differentiation Gastric cancer Clic2 |
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References | Y Ueno (666_CR12) 2019; 7 K Yoshihara (666_CR15) 2013; 4 P Zhang (666_CR36) 2019; 27 A Ianevski (666_CR35) 2022; 13 MS Carro (666_CR32) 2010; 463 DR Littler (666_CR13) 2010; 584 P Laurén (666_CR1) 1965; 64 X Qin (666_CR20) 2018; 8 B Manori (666_CR9) 2024; 15 M Colella (666_CR44) 2024; 16 F Albano (666_CR39) 2021; 22 S Müller-Dott (666_CR30) 2023; 51 SY Hong (666_CR28) 2023; 14 T Xu (666_CR14) 2020; 12 D Briukhovetska (666_CR27) 2021; 21 A Tsubosaka (666_CR37) 2023; 42 A Arcucci (666_CR43) 2011; 25 T Seidlitz (666_CR29) 2021; 28 P Iyer (666_CR2) 2020; 5 E Argenzio (666_CR6) 2016; 129 AJ Bass (666_CR3) 2014; 513 EW Baxter (666_CR17) 2020; 478 S Chen (666_CR18) 2023; 8 Y Hao (666_CR34) 2023; 42 AA Margolin (666_CR31) 2006; 7 S Ozaki (666_CR11) 2021; 23 L Greco (666_CR21) 2023; 14 I Guerriero (666_CR38) 2019; 4900 G Fiume (666_CR42) 2016; 17 S Russi (666_CR5) 2022; 14 STM Chung (666_CR26) 2017; 16 M Metzemaekers (666_CR19) 2020; 17 S Ozaki (666_CR7) 2022; 14 Y Ueno (666_CR23) 2019; 7 V Randrian (666_CR22) 2021; 13 H Yamaguchi (666_CR4) 2024; 5 H Singh (666_CR8) 2010; 584 M Peretti (666_CR10) 2015; 1848 MJ Alvarez (666_CR33) 2016; 48 MG Filippone (666_CR41) 2014; 15 M Israr (666_CR25) 2022; 87 V Kumar (666_CR16) 2022; 12 F Albano (666_CR40) 2018; 9 DCT Palomino (666_CR24) 2015; 13 |
References_xml | – volume: 478 year: 2020 ident: 666_CR17 publication-title: J Immunol Methods doi: 10.1016/j.jim.2019.112721 – volume: 27 start-page: 1934 year: 2019 ident: 666_CR36 publication-title: Cell Rep doi: 10.1016/j.celrep.2019.04.052 – volume: 5 year: 2024 ident: 666_CR4 publication-title: Cell Rep Med doi: 10.1016/j.xcrm.2024.101621 – volume: 14 start-page: 352 issue: 6 year: 2023 ident: 666_CR28 publication-title: Cell Death Dis doi: 10.1038/s41419-023-05876-z – volume: 513 start-page: 202 year: 2014 ident: 666_CR3 publication-title: Nature doi: 10.1038/nature13480 – volume: 16 start-page: 1 year: 2017 ident: 666_CR26 publication-title: Mol Cancer doi: 10.1186/s12943-017-0606-y – volume: 48 start-page: 838 year: 2016 ident: 666_CR33 publication-title: Nat Genet doi: 10.1038/ng.3593 – volume: 1848 start-page: 2523 year: 2015 ident: 666_CR10 publication-title: Biochim Biophys Acta (BBA): Biomembr. doi: 10.1016/j.bbamem.2014.12.012 – volume: 25 start-page: 647 issue: 4 year: 2011 ident: 666_CR43 publication-title: J Biol Regul Homeost Agents – volume: 15 start-page: 2085 year: 2024 ident: 666_CR9 publication-title: Nat Commun doi: 10.1038/s41467-024-46301-z – volume: 17 start-page: 433 year: 2020 ident: 666_CR19 publication-title: Cell Mol Immunol doi: 10.1038/s41423-020-0412-0 – volume: 42 year: 2023 ident: 666_CR37 publication-title: Cell Rep doi: 10.1016/j.celrep.2023.113236 – volume: 7 start-page: 1593775 year: 2019 ident: 666_CR12 publication-title: Tissue Barriers doi: 10.1080/21688370.2019.1593775 – volume: 584 start-page: 2093 year: 2010 ident: 666_CR13 publication-title: FEBS Lett doi: 10.1016/j.febslet.2010.01.027 – volume: 51 start-page: 10934 year: 2023 ident: 666_CR30 publication-title: Nucleic Acids Res doi: 10.1093/nar/gkad841 – volume: 16 start-page: 2370 issue: 13 year: 2024 ident: 666_CR44 publication-title: Cancers doi: 10.3390/cancers16132370 – volume: 42 start-page: 293 year: 2023 ident: 666_CR34 publication-title: Nat Biotechnol doi: 10.1038/s41587-023-01767-y – volume: 584 start-page: 2112 year: 2010 ident: 666_CR8 publication-title: FEBS Lett doi: 10.1016/j.febslet.2010.03.013 – volume: 7 start-page: S7 year: 2006 ident: 666_CR31 publication-title: BMC Bioinf doi: 10.1186/1471-2105-7-S1-S7 – volume: 12 start-page: 17305 year: 2020 ident: 666_CR14 publication-title: Aging doi: 10.18632/aging.103712 – volume: 8 start-page: 921 year: 2018 ident: 666_CR20 publication-title: Theranostics doi: 10.7150/thno.22182 – volume: 7 start-page: 1593775 issue: 1 year: 2019 ident: 666_CR23 publication-title: Tissue Barriers doi: 10.1080/21688370.2019.1593775 – volume: 87 start-page: 170 year: 2022 ident: 666_CR25 publication-title: Semin Cancer Biol doi: 10.1016/j.semcancer.2022.11.010 – volume: 8 start-page: 207 year: 2023 ident: 666_CR18 publication-title: Signal Transduct Target Ther doi: 10.1038/s41392-023-01452-1 – volume: 14 start-page: 1169 year: 2023 ident: 666_CR21 publication-title: Genes doi: 10.3390/genes14061169 – volume: 15 start-page: 1 year: 2014 ident: 666_CR41 publication-title: BMC Mol Biol doi: 10.1186/1471-2199-15-21 – volume: 129 start-page: 4165 year: 2016 ident: 666_CR6 publication-title: J Cell Sci doi: 10.1242/jcs.189795 – volume: 23 start-page: 754 year: 2021 ident: 666_CR11 publication-title: Neoplasia doi: 10.1016/j.neo.2021.06.001 – volume: 4 start-page: 2612 year: 2013 ident: 666_CR15 publication-title: Nat Commun doi: 10.1038/ncomms3612 – volume: 13 start-page: 3063 year: 2021 ident: 666_CR22 publication-title: Immuno-Res Emerg Therapies. Cancers – volume: 21 start-page: 481 year: 2021 ident: 666_CR27 publication-title: Nat Rev Cancer doi: 10.1038/s41568-021-00363-z – volume: 22 start-page: 9379 issue: 17 year: 2021 ident: 666_CR39 publication-title: Int J Mol Sci doi: 10.3390/ijms22179379 – volume: 14 start-page: 4890 year: 2022 ident: 666_CR7 publication-title: Cancers doi: 10.3390/cancers14194890 – volume: 9 start-page: 13 issue: 1 year: 2018 ident: 666_CR40 publication-title: Cell Death Dis doi: 10.1038/s41419-017-0026-3 – volume: 17 start-page: 1848 issue: 11 year: 2016 ident: 666_CR42 publication-title: Int J Mol Sci doi: 10.3390/ijms17111848 – volume: 463 start-page: 318 year: 2010 ident: 666_CR32 publication-title: Nature doi: 10.1038/nature08712 – volume: 4900 start-page: 4900 issue: 20 year: 2019 ident: 666_CR38 publication-title: Int J Mol Sci doi: 10.3390/ijms20194900 – volume: 64 start-page: 31 year: 1965 ident: 666_CR1 publication-title: Acta Pathol Microbiol Scand doi: 10.1111/apm.1965.64.1.31 – volume: 13 start-page: 469 year: 2015 ident: 666_CR24 publication-title: Einstein doi: 10.1590/S1679-45082015RB3438 – volume: 5 start-page: 52 year: 2020 ident: 666_CR2 publication-title: Transl Gastroenterol Hepatol doi: 10.21037/tgh.2020.01.02 – volume: 12 start-page: 670 year: 2022 ident: 666_CR16 publication-title: Cancer Discov doi: 10.1158/2159-8290.CD-21-0683 – volume: 13 start-page: 1 year: 2022 ident: 666_CR35 publication-title: Nat Commun doi: 10.1038/s41467-022-28803-w – volume: 28 start-page: 68 year: 2021 ident: 666_CR29 publication-title: Cell Death Differ doi: 10.1038/s41418-020-00662-2 – volume: 14 start-page: 4961 year: 2022 ident: 666_CR5 publication-title: Cancers doi: 10.3390/cancers14194961 |
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Snippet | Chloride intracellular channels (CLICs) are a family of six evolutionarily conserved proteins with diverse functions. Previously, we identified CLIC2, as the... Abstract Chloride intracellular channels (CLICs) are a family of six evolutionarily conserved proteins with diverse functions. Previously, we identified CLIC2,... |
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SubjectTerms | Analysis Anopheles Biomedical and Life Sciences Brain cancer Cancer Care and treatment CD11b antigen CD11c antigen CD80 antigen CD86 antigen Cell differentiation Cell Differentiation - genetics Cells Chloride channels Chloride Channels - genetics Chloride Channels - metabolism Clic2 Cloning Development and progression Diagnosis Differentiation Disease Endothelial cells Endothelium Fibroblasts Gastric cancer Gastric microenvironment Gene expression Genetic aspects Genomes Health aspects Humans Immunosuppression Immunotherapy Life Sciences Localization Macrophages Macrophages - metabolism Medical prognosis Microenvironments Monocytes Osteoprotegerin Patient outcomes Phosphatases Phosphorylation Proteins SHP-1 protein Signal transduction Stat3 protein Stomach cancer Stomach Neoplasms - genetics Stomach Neoplasms - immunology Stomach Neoplasms - metabolism Tumor microenvironment Tumors |
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Title | CLIC2 regulates immunosuppression and macrophage differentiation in genomically stable gastric cancer |
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