Role of PD-L1 Expression during the Progression of Submucosal Gastric Cancer
Introduction: Programmed death-ligand 1 (PD-L1) expression is a prognostic marker for gastric cancer that correlates with tumor diameter and depth of penetration. But the role of PD-L1 and mechanism(s) employed in the initial phase of invasion in early gastric cancer is yet to be understood. Objecti...
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creator | Ubukata, Yasunari Ogata, Kyoichi Sohda, Makoto Yokobori, Takehiko Shimoda, Yuki Handa, Tadashi Nakazawa, Nobuhiro Kimura, Akiharu Kogure, Norimichi Sano, Akihiko Sakai, Makoto Ogawa, Hiroomi Kuwano, Hiroyuki Shirabe, Ken Oyama, Tetsunari Saeki, Hiroshi |
description | Introduction: Programmed death-ligand 1 (PD-L1) expression is a prognostic marker for gastric cancer that correlates with tumor diameter and depth of penetration. But the role of PD-L1 and mechanism(s) employed in the initial phase of invasion in early gastric cancer is yet to be understood. Objective: This study aims to elucidate the role of PD-L1 during the progression of gastric cancer, specifically invading the submucosa beyond the lamina muscularis mucosa. Methods: Using 107 patients with pathological submucosal gastric cancer, we determined the expression of PD-L1 based on the staining of the cell membrane or cytoplasm of tumor cells in the central and invasive front of the tumor. Samples were categorized into 3 groups based on the intensity of PD-L1 expression. CD8 + lymphocytes expressing PD-1 and CD163 + macrophages were used to determine the number of cell nuclei at the invasive front, similar to PD-L1. CMTM6 levels were determined and used to stratify samples into 3 groups. Results: PD-L1 expression was higher in the invasive front (26.2%) than in the central portion of the tumors (7.4%; p < 0.001). Moreover, lymphatic and vascular invasion were more frequently observed in samples with high levels of PD-L1 (lymphatic invasion: 60.7 vs. 35.4%, p = 0.0026, and vascular invasion: 39.3 vs. 16.5%, p = 0.0018). There was no correlation between PD-L1 expression and the levels of PD-1, CD8, CD163, and CMTM6. Conclusions: PD-L1-expressing cancer cells at the invasive front of gastric cancer influence the initial stages of tumor invasion and lymphovascular permeation in early-stage gastric cancers. Immune checkpoint signaling may be the driving force in the invasive front during the invasion of the submucosa beyond the lamina muscularis mucosa. |
doi_str_mv | 10.1159/000509033 |
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But the role of PD-L1 and mechanism(s) employed in the initial phase of invasion in early gastric cancer is yet to be understood. Objective: This study aims to elucidate the role of PD-L1 during the progression of gastric cancer, specifically invading the submucosa beyond the lamina muscularis mucosa. Methods: Using 107 patients with pathological submucosal gastric cancer, we determined the expression of PD-L1 based on the staining of the cell membrane or cytoplasm of tumor cells in the central and invasive front of the tumor. Samples were categorized into 3 groups based on the intensity of PD-L1 expression. CD8 + lymphocytes expressing PD-1 and CD163 + macrophages were used to determine the number of cell nuclei at the invasive front, similar to PD-L1. CMTM6 levels were determined and used to stratify samples into 3 groups. Results: PD-L1 expression was higher in the invasive front (26.2%) than in the central portion of the tumors (7.4%; p < 0.001). Moreover, lymphatic and vascular invasion were more frequently observed in samples with high levels of PD-L1 (lymphatic invasion: 60.7 vs. 35.4%, p = 0.0026, and vascular invasion: 39.3 vs. 16.5%, p = 0.0018). There was no correlation between PD-L1 expression and the levels of PD-1, CD8, CD163, and CMTM6. Conclusions: PD-L1-expressing cancer cells at the invasive front of gastric cancer influence the initial stages of tumor invasion and lymphovascular permeation in early-stage gastric cancers. Immune checkpoint signaling may be the driving force in the invasive front during the invasion of the submucosa beyond the lamina muscularis mucosa.</description><identifier>ISSN: 0030-2414</identifier><identifier>EISSN: 1423-0232</identifier><identifier>DOI: 10.1159/000509033</identifier><identifier>PMID: 33113541</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Aged ; Analysis ; Antigens, CD - genetics ; Antigens, Differentiation, Myelomonocytic - genetics ; B7-H1 Antigen - genetics ; Biomarkers, Tumor - genetics ; Care and treatment ; CD8-Positive T-Lymphocytes - metabolism ; CD8-Positive T-Lymphocytes - pathology ; Cell differentiation ; Clinical Study ; Development and progression ; Diagnosis ; Disease Progression ; Female ; Gene Expression Regulation, Neoplastic - genetics ; Health aspects ; Humans ; Ligands (Biochemistry) ; Lymphocytes, Tumor-Infiltrating - metabolism ; Lymphocytes, Tumor-Infiltrating - pathology ; Male ; Middle Aged ; Prognosis ; Receptors, Cell Surface - genetics ; Stomach cancer ; Stomach Neoplasms - genetics ; Stomach Neoplasms - metabolism ; Stomach Neoplasms - pathology ; Submucous Plexus - metabolism ; Submucous Plexus - pathology ; Tumor proteins</subject><ispartof>Oncology, 2021-01, Vol.99 (1), p.15-22</ispartof><rights>2020 S. Karger AG, Basel</rights><rights>2020 S. Karger AG, Basel.</rights><rights>COPYRIGHT 2021 S. Karger AG</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c533t-16dc953896407d89de647fc0bb3245573ff7fca671a597dca4849af8c3ddabac3</citedby><cites>FETCH-LOGICAL-c533t-16dc953896407d89de647fc0bb3245573ff7fca671a597dca4849af8c3ddabac3</cites><orcidid>0000-0002-9531-5157 ; 0000-0003-3284-4796 ; 0000-0003-0860-3132 ; 0000-0001-7447-7512</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,2422,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33113541$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ubukata, Yasunari</creatorcontrib><creatorcontrib>Ogata, Kyoichi</creatorcontrib><creatorcontrib>Sohda, Makoto</creatorcontrib><creatorcontrib>Yokobori, Takehiko</creatorcontrib><creatorcontrib>Shimoda, Yuki</creatorcontrib><creatorcontrib>Handa, Tadashi</creatorcontrib><creatorcontrib>Nakazawa, Nobuhiro</creatorcontrib><creatorcontrib>Kimura, Akiharu</creatorcontrib><creatorcontrib>Kogure, Norimichi</creatorcontrib><creatorcontrib>Sano, Akihiko</creatorcontrib><creatorcontrib>Sakai, Makoto</creatorcontrib><creatorcontrib>Ogawa, Hiroomi</creatorcontrib><creatorcontrib>Kuwano, Hiroyuki</creatorcontrib><creatorcontrib>Shirabe, Ken</creatorcontrib><creatorcontrib>Oyama, Tetsunari</creatorcontrib><creatorcontrib>Saeki, Hiroshi</creatorcontrib><title>Role of PD-L1 Expression during the Progression of Submucosal Gastric Cancer</title><title>Oncology</title><addtitle>Oncology</addtitle><description>Introduction: Programmed death-ligand 1 (PD-L1) expression is a prognostic marker for gastric cancer that correlates with tumor diameter and depth of penetration. But the role of PD-L1 and mechanism(s) employed in the initial phase of invasion in early gastric cancer is yet to be understood. Objective: This study aims to elucidate the role of PD-L1 during the progression of gastric cancer, specifically invading the submucosa beyond the lamina muscularis mucosa. Methods: Using 107 patients with pathological submucosal gastric cancer, we determined the expression of PD-L1 based on the staining of the cell membrane or cytoplasm of tumor cells in the central and invasive front of the tumor. Samples were categorized into 3 groups based on the intensity of PD-L1 expression. CD8 + lymphocytes expressing PD-1 and CD163 + macrophages were used to determine the number of cell nuclei at the invasive front, similar to PD-L1. CMTM6 levels were determined and used to stratify samples into 3 groups. Results: PD-L1 expression was higher in the invasive front (26.2%) than in the central portion of the tumors (7.4%; p < 0.001). Moreover, lymphatic and vascular invasion were more frequently observed in samples with high levels of PD-L1 (lymphatic invasion: 60.7 vs. 35.4%, p = 0.0026, and vascular invasion: 39.3 vs. 16.5%, p = 0.0018). There was no correlation between PD-L1 expression and the levels of PD-1, CD8, CD163, and CMTM6. Conclusions: PD-L1-expressing cancer cells at the invasive front of gastric cancer influence the initial stages of tumor invasion and lymphovascular permeation in early-stage gastric cancers. Immune checkpoint signaling may be the driving force in the invasive front during the invasion of the submucosa beyond the lamina muscularis mucosa.</description><subject>Aged</subject><subject>Analysis</subject><subject>Antigens, CD - genetics</subject><subject>Antigens, Differentiation, Myelomonocytic - genetics</subject><subject>B7-H1 Antigen - genetics</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Care and treatment</subject><subject>CD8-Positive T-Lymphocytes - metabolism</subject><subject>CD8-Positive T-Lymphocytes - pathology</subject><subject>Cell differentiation</subject><subject>Clinical Study</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Gene Expression Regulation, Neoplastic - genetics</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Ligands (Biochemistry)</subject><subject>Lymphocytes, Tumor-Infiltrating - metabolism</subject><subject>Lymphocytes, Tumor-Infiltrating - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Prognosis</subject><subject>Receptors, Cell Surface - genetics</subject><subject>Stomach cancer</subject><subject>Stomach Neoplasms - genetics</subject><subject>Stomach Neoplasms - metabolism</subject><subject>Stomach Neoplasms - pathology</subject><subject>Submucous Plexus - metabolism</subject><subject>Submucous Plexus - pathology</subject><subject>Tumor proteins</subject><issn>0030-2414</issn><issn>1423-0232</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0UtLxDAQAOAgiq6Pg3eRgiB6qCadpGmPsj6hoPg4h2weu9VusyYt6L83y66rguQQMnwzYWYQ2if4jBBWnmOMGS4xwBoaEJpBijPI1tEAY8BpRgndQtshvEbGGc030RYAIcAoGaDq0TUmcTZ5uEwrklx9zLwJoXZtontft-Okm5jkwbvxdzjSp3407ZULskluZOh8rZKhbJXxu2jDyiaYveW9g16ur56Ht2l1f3M3vKhSxQC6lORalQyKMqeY66LUJqfcKjwaQUYZ42BtfMqcE8lKrpWkBS2lLRRoLUdSwQ46WdSdeffem9CJaR2UaRrZGtcHMa9SUOCcRnq0oGPZGFG31nVeqjkXF3lRcM6hhKjO_lHxaDOtlWuNrWP8T8Lxr4SJkU03Ca7puzii8BeeLqDyLgRvrJj5eir9pyBYzJcnVsuL9nDZVhyw0Sv5va2fZt6kHxu_AvfDalFCzLSN6uBftfzlC7lepYE</recordid><startdate>20210101</startdate><enddate>20210101</enddate><creator>Ubukata, Yasunari</creator><creator>Ogata, Kyoichi</creator><creator>Sohda, Makoto</creator><creator>Yokobori, Takehiko</creator><creator>Shimoda, Yuki</creator><creator>Handa, Tadashi</creator><creator>Nakazawa, Nobuhiro</creator><creator>Kimura, Akiharu</creator><creator>Kogure, Norimichi</creator><creator>Sano, Akihiko</creator><creator>Sakai, Makoto</creator><creator>Ogawa, Hiroomi</creator><creator>Kuwano, Hiroyuki</creator><creator>Shirabe, Ken</creator><creator>Oyama, Tetsunari</creator><creator>Saeki, Hiroshi</creator><general>S. Karger AG</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/0000-0002-9531-5157</orcidid><orcidid>https://orcid.org/0000-0003-3284-4796</orcidid><orcidid>https://orcid.org/0000-0003-0860-3132</orcidid><orcidid>https://orcid.org/0000-0001-7447-7512</orcidid></search><sort><creationdate>20210101</creationdate><title>Role of PD-L1 Expression during the Progression of Submucosal Gastric Cancer</title><author>Ubukata, Yasunari ; Ogata, Kyoichi ; Sohda, Makoto ; Yokobori, Takehiko ; Shimoda, Yuki ; Handa, Tadashi ; Nakazawa, Nobuhiro ; Kimura, Akiharu ; Kogure, Norimichi ; Sano, Akihiko ; Sakai, Makoto ; Ogawa, Hiroomi ; Kuwano, Hiroyuki ; Shirabe, Ken ; Oyama, Tetsunari ; Saeki, Hiroshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c533t-16dc953896407d89de647fc0bb3245573ff7fca671a597dca4849af8c3ddabac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Aged</topic><topic>Analysis</topic><topic>Antigens, CD - genetics</topic><topic>Antigens, Differentiation, Myelomonocytic - genetics</topic><topic>B7-H1 Antigen - genetics</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Care and treatment</topic><topic>CD8-Positive T-Lymphocytes - metabolism</topic><topic>CD8-Positive T-Lymphocytes - pathology</topic><topic>Cell differentiation</topic><topic>Clinical Study</topic><topic>Development and progression</topic><topic>Diagnosis</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Gene Expression Regulation, Neoplastic - genetics</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Ligands (Biochemistry)</topic><topic>Lymphocytes, Tumor-Infiltrating - metabolism</topic><topic>Lymphocytes, Tumor-Infiltrating - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Prognosis</topic><topic>Receptors, Cell Surface - genetics</topic><topic>Stomach cancer</topic><topic>Stomach Neoplasms - genetics</topic><topic>Stomach Neoplasms - metabolism</topic><topic>Stomach Neoplasms - pathology</topic><topic>Submucous Plexus - metabolism</topic><topic>Submucous Plexus - pathology</topic><topic>Tumor proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ubukata, Yasunari</creatorcontrib><creatorcontrib>Ogata, Kyoichi</creatorcontrib><creatorcontrib>Sohda, Makoto</creatorcontrib><creatorcontrib>Yokobori, Takehiko</creatorcontrib><creatorcontrib>Shimoda, Yuki</creatorcontrib><creatorcontrib>Handa, Tadashi</creatorcontrib><creatorcontrib>Nakazawa, Nobuhiro</creatorcontrib><creatorcontrib>Kimura, Akiharu</creatorcontrib><creatorcontrib>Kogure, Norimichi</creatorcontrib><creatorcontrib>Sano, Akihiko</creatorcontrib><creatorcontrib>Sakai, Makoto</creatorcontrib><creatorcontrib>Ogawa, Hiroomi</creatorcontrib><creatorcontrib>Kuwano, Hiroyuki</creatorcontrib><creatorcontrib>Shirabe, Ken</creatorcontrib><creatorcontrib>Oyama, Tetsunari</creatorcontrib><creatorcontrib>Saeki, Hiroshi</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>Oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ubukata, Yasunari</au><au>Ogata, Kyoichi</au><au>Sohda, Makoto</au><au>Yokobori, Takehiko</au><au>Shimoda, Yuki</au><au>Handa, Tadashi</au><au>Nakazawa, Nobuhiro</au><au>Kimura, Akiharu</au><au>Kogure, Norimichi</au><au>Sano, Akihiko</au><au>Sakai, Makoto</au><au>Ogawa, Hiroomi</au><au>Kuwano, Hiroyuki</au><au>Shirabe, Ken</au><au>Oyama, Tetsunari</au><au>Saeki, Hiroshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of PD-L1 Expression during the Progression of Submucosal Gastric Cancer</atitle><jtitle>Oncology</jtitle><addtitle>Oncology</addtitle><date>2021-01-01</date><risdate>2021</risdate><volume>99</volume><issue>1</issue><spage>15</spage><epage>22</epage><pages>15-22</pages><issn>0030-2414</issn><eissn>1423-0232</eissn><abstract>Introduction: Programmed death-ligand 1 (PD-L1) expression is a prognostic marker for gastric cancer that correlates with tumor diameter and depth of penetration. But the role of PD-L1 and mechanism(s) employed in the initial phase of invasion in early gastric cancer is yet to be understood. Objective: This study aims to elucidate the role of PD-L1 during the progression of gastric cancer, specifically invading the submucosa beyond the lamina muscularis mucosa. Methods: Using 107 patients with pathological submucosal gastric cancer, we determined the expression of PD-L1 based on the staining of the cell membrane or cytoplasm of tumor cells in the central and invasive front of the tumor. Samples were categorized into 3 groups based on the intensity of PD-L1 expression. CD8 + lymphocytes expressing PD-1 and CD163 + macrophages were used to determine the number of cell nuclei at the invasive front, similar to PD-L1. CMTM6 levels were determined and used to stratify samples into 3 groups. Results: PD-L1 expression was higher in the invasive front (26.2%) than in the central portion of the tumors (7.4%; p < 0.001). Moreover, lymphatic and vascular invasion were more frequently observed in samples with high levels of PD-L1 (lymphatic invasion: 60.7 vs. 35.4%, p = 0.0026, and vascular invasion: 39.3 vs. 16.5%, p = 0.0018). There was no correlation between PD-L1 expression and the levels of PD-1, CD8, CD163, and CMTM6. Conclusions: PD-L1-expressing cancer cells at the invasive front of gastric cancer influence the initial stages of tumor invasion and lymphovascular permeation in early-stage gastric cancers. Immune checkpoint signaling may be the driving force in the invasive front during the invasion of the submucosa beyond the lamina muscularis mucosa.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>33113541</pmid><doi>10.1159/000509033</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-9531-5157</orcidid><orcidid>https://orcid.org/0000-0003-3284-4796</orcidid><orcidid>https://orcid.org/0000-0003-0860-3132</orcidid><orcidid>https://orcid.org/0000-0001-7447-7512</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aged Analysis Antigens, CD - genetics Antigens, Differentiation, Myelomonocytic - genetics B7-H1 Antigen - genetics Biomarkers, Tumor - genetics Care and treatment CD8-Positive T-Lymphocytes - metabolism CD8-Positive T-Lymphocytes - pathology Cell differentiation Clinical Study Development and progression Diagnosis Disease Progression Female Gene Expression Regulation, Neoplastic - genetics Health aspects Humans Ligands (Biochemistry) Lymphocytes, Tumor-Infiltrating - metabolism Lymphocytes, Tumor-Infiltrating - pathology Male Middle Aged Prognosis Receptors, Cell Surface - genetics Stomach cancer Stomach Neoplasms - genetics Stomach Neoplasms - metabolism Stomach Neoplasms - pathology Submucous Plexus - metabolism Submucous Plexus - pathology Tumor proteins |
title | Role of PD-L1 Expression during the Progression of Submucosal Gastric Cancer |
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