Loading…
Prognostic Significance of GPR55 mRNA Expression in Colon Cancer
G protein-coupled receptor 55 (GPR55) probably plays a role in innate immunity and tumor immunosurveillance through its effect on immune cells, such as T cells and NK cells. In this study, the prognostic value of GPR55 in colon cancer (CC) was investigated. mRNA expression levels of GPR55 were deter...
Saved in:
Published in: | International journal of molecular sciences 2022-05, Vol.23 (9), p.4556 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c585t-7ddedb0f8cc55dc4cf7cbda700b255dbd7e1c41bc6f4f6f302c8464b3afe18b73 |
---|---|
cites | cdi_FETCH-LOGICAL-c585t-7ddedb0f8cc55dc4cf7cbda700b255dbd7e1c41bc6f4f6f302c8464b3afe18b73 |
container_end_page | |
container_issue | 9 |
container_start_page | 4556 |
container_title | International journal of molecular sciences |
container_volume | 23 |
creator | Ismail, Hager Tarek H AbdelMageed, Manar Lindmark, Gudrun Hammarström, Marie-Louise Hammarström, Sten Sitohy, Basel |
description | G protein-coupled receptor 55 (GPR55) probably plays a role in innate immunity and tumor immunosurveillance through its effect on immune cells, such as T cells and NK cells. In this study, the prognostic value of GPR55 in colon cancer (CC) was investigated. mRNA expression levels of GPR55 were determined in 382 regional lymph nodes of 121 CC patients with 12 years observation time after curative surgery. The same clinical material had previously been analyzed for expression levels of CEA, CXCL16, CXCL17, GPR35 V2/3 and LGR5 mRNAs. Clinical cutoffs of 0.1365 copies/18S rRNA unit for GPR55 and 0.1481 for the GPR55/CEA ratio were applied to differentiate between the high- and low-GPR55 expression groups. Kaplan-Meier survival analysis and Cox regression risk analysis were used to determine prognostic value. Improved discrimination between the two groups was achieved by combining GPR55 with CEA, CXCL16 or CXCL17 compared with GPR55 alone. The best result was obtained using the GPR55/CEA ratio, with an increased mean survival time of 14 and 33 months at 5 and 12 years observation time, respectively (
= 0.0003 and
= 0.003) for the high-GPR55/CEA group. The explanation for the observed improvement is most likely that GPR55 is a marker for T cells and B cells in lymph nodes, whereas CEA, CXCL16 and CXCL17, are markers for tumor cells of epithelial origin. |
doi_str_mv | 10.3390/ijms23094556 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_598ad944193a479e83d5f23d77606369</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_598ad944193a479e83d5f23d77606369</doaj_id><sourcerecordid>2664807634</sourcerecordid><originalsourceid>FETCH-LOGICAL-c585t-7ddedb0f8cc55dc4cf7cbda700b255dbd7e1c41bc6f4f6f302c8464b3afe18b73</originalsourceid><addsrcrecordid>eNp1kktvEzEQgFcIRB9w44xW4sKhgfF7fUGNQimVIqjK42p5_QiOdtfBzvL493ibUiVIHEa2xp8_z8hTVc8QvCJEwuuw7jMmIClj_EF1jCjGMwAuHu7tj6qTnNcAmGAmH1dHpLBYUnFcnV-nuBpi3gZTfwqrIfhg9GBcHX19eX3DWN3ffJjXF782yeUc4lCHoV7ErmwWE5eeVI-87rJ7ereeVl_eXXxevJ8tP15eLebLmWEN286Etc624BtjGLOGGi9Ma7UAaHFJtFY4ZChqDffUc08Am4Zy2hLtHWpaQU6rq53XRr1WmxR6nX6rqIO6TcS0UjqVLjqnmGy0lZQiSTQV0jXEMo-JFYIDJ1wW13Lnyj_dZmwPbN24KdGWULmoKNPGg1G61K4oEKGalmBlkGaOlEccTLrZf3Vvw9f5bXFjPyokKeGo8G92fIF7Z40btkl3B9cOT4bwTa3iDyURcGCkCF7eCVL8Prq8VX3IxnWdHlwcs8Kc0wYEJ7SgL_5B13FMQ_mpiSIgZCOmis52lEkx5-T8fTEI1DRlan_KCv58v4F7-O9YkT8FIczA</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2663079871</pqid></control><display><type>article</type><title>Prognostic Significance of GPR55 mRNA Expression in Colon Cancer</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Ismail, Hager Tarek H ; AbdelMageed, Manar ; Lindmark, Gudrun ; Hammarström, Marie-Louise ; Hammarström, Sten ; Sitohy, Basel</creator><creatorcontrib>Ismail, Hager Tarek H ; AbdelMageed, Manar ; Lindmark, Gudrun ; Hammarström, Marie-Louise ; Hammarström, Sten ; Sitohy, Basel</creatorcontrib><description>G protein-coupled receptor 55 (GPR55) probably plays a role in innate immunity and tumor immunosurveillance through its effect on immune cells, such as T cells and NK cells. In this study, the prognostic value of GPR55 in colon cancer (CC) was investigated. mRNA expression levels of GPR55 were determined in 382 regional lymph nodes of 121 CC patients with 12 years observation time after curative surgery. The same clinical material had previously been analyzed for expression levels of CEA, CXCL16, CXCL17, GPR35 V2/3 and LGR5 mRNAs. Clinical cutoffs of 0.1365 copies/18S rRNA unit for GPR55 and 0.1481 for the GPR55/CEA ratio were applied to differentiate between the high- and low-GPR55 expression groups. Kaplan-Meier survival analysis and Cox regression risk analysis were used to determine prognostic value. Improved discrimination between the two groups was achieved by combining GPR55 with CEA, CXCL16 or CXCL17 compared with GPR55 alone. The best result was obtained using the GPR55/CEA ratio, with an increased mean survival time of 14 and 33 months at 5 and 12 years observation time, respectively (
= 0.0003 and
= 0.003) for the high-GPR55/CEA group. The explanation for the observed improvement is most likely that GPR55 is a marker for T cells and B cells in lymph nodes, whereas CEA, CXCL16 and CXCL17, are markers for tumor cells of epithelial origin.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms23094556</identifier><identifier>PMID: 35562947</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Basic Medicine ; Biomarkers ; Biomarkers, Tumor - genetics ; Biomarkers, Tumor - metabolism ; Cancer and Oncology ; Cancer och onkologi ; Carcinoembryonic Antigen - genetics ; CEA ; Cell and Molecular Biology ; Cell- och molekylärbiologi ; Clinical Medicine ; Colon ; Colon cancer ; Colonic Neoplasms - genetics ; Colonic Neoplasms - pathology ; Colorectal cancer ; CXCL16 ; CXCL16 protein ; CXCL17 ; Gene expression ; GPR55 ; Humans ; Immune system ; Immunosurveillance ; Innate immunity ; Klinisk medicin ; Lymph nodes ; Lymphatic system ; Lymphocytes ; Lymphocytes B ; Lymphocytes T ; Markers ; Medical and Health Sciences ; Medical prognosis ; Medicin och hälsovetenskap ; Medicinska och farmaceutiska grundvetenskaper ; Patients ; Prognosis ; qRT-PCR ; Receptors, Cannabinoid ; regional lymph nodes ; Risk analysis ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; rRNA 18S ; Small intestine ; Survival ; Tumor cells ; Tumors</subject><ispartof>International journal of molecular sciences, 2022-05, Vol.23 (9), p.4556</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c585t-7ddedb0f8cc55dc4cf7cbda700b255dbd7e1c41bc6f4f6f302c8464b3afe18b73</citedby><cites>FETCH-LOGICAL-c585t-7ddedb0f8cc55dc4cf7cbda700b255dbd7e1c41bc6f4f6f302c8464b3afe18b73</cites><orcidid>0000-0001-8803-4798 ; 0000-0003-3631-6122 ; 0000-0002-4010-4002 ; 0000-0001-9215-7758</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2663079871/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2663079871?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35562947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-194361$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttps://lup.lub.lu.se/record/545acf0c-ab0f-4037-8b32-c1a5e3d94e09$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Ismail, Hager Tarek H</creatorcontrib><creatorcontrib>AbdelMageed, Manar</creatorcontrib><creatorcontrib>Lindmark, Gudrun</creatorcontrib><creatorcontrib>Hammarström, Marie-Louise</creatorcontrib><creatorcontrib>Hammarström, Sten</creatorcontrib><creatorcontrib>Sitohy, Basel</creatorcontrib><title>Prognostic Significance of GPR55 mRNA Expression in Colon Cancer</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>G protein-coupled receptor 55 (GPR55) probably plays a role in innate immunity and tumor immunosurveillance through its effect on immune cells, such as T cells and NK cells. In this study, the prognostic value of GPR55 in colon cancer (CC) was investigated. mRNA expression levels of GPR55 were determined in 382 regional lymph nodes of 121 CC patients with 12 years observation time after curative surgery. The same clinical material had previously been analyzed for expression levels of CEA, CXCL16, CXCL17, GPR35 V2/3 and LGR5 mRNAs. Clinical cutoffs of 0.1365 copies/18S rRNA unit for GPR55 and 0.1481 for the GPR55/CEA ratio were applied to differentiate between the high- and low-GPR55 expression groups. Kaplan-Meier survival analysis and Cox regression risk analysis were used to determine prognostic value. Improved discrimination between the two groups was achieved by combining GPR55 with CEA, CXCL16 or CXCL17 compared with GPR55 alone. The best result was obtained using the GPR55/CEA ratio, with an increased mean survival time of 14 and 33 months at 5 and 12 years observation time, respectively (
= 0.0003 and
= 0.003) for the high-GPR55/CEA group. The explanation for the observed improvement is most likely that GPR55 is a marker for T cells and B cells in lymph nodes, whereas CEA, CXCL16 and CXCL17, are markers for tumor cells of epithelial origin.</description><subject>Basic Medicine</subject><subject>Biomarkers</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Cancer and Oncology</subject><subject>Cancer och onkologi</subject><subject>Carcinoembryonic Antigen - genetics</subject><subject>CEA</subject><subject>Cell and Molecular Biology</subject><subject>Cell- och molekylärbiologi</subject><subject>Clinical Medicine</subject><subject>Colon</subject><subject>Colon cancer</subject><subject>Colonic Neoplasms - genetics</subject><subject>Colonic Neoplasms - pathology</subject><subject>Colorectal cancer</subject><subject>CXCL16</subject><subject>CXCL16 protein</subject><subject>CXCL17</subject><subject>Gene expression</subject><subject>GPR55</subject><subject>Humans</subject><subject>Immune system</subject><subject>Immunosurveillance</subject><subject>Innate immunity</subject><subject>Klinisk medicin</subject><subject>Lymph nodes</subject><subject>Lymphatic system</subject><subject>Lymphocytes</subject><subject>Lymphocytes B</subject><subject>Lymphocytes T</subject><subject>Markers</subject><subject>Medical and Health Sciences</subject><subject>Medical prognosis</subject><subject>Medicin och hälsovetenskap</subject><subject>Medicinska och farmaceutiska grundvetenskaper</subject><subject>Patients</subject><subject>Prognosis</subject><subject>qRT-PCR</subject><subject>Receptors, Cannabinoid</subject><subject>regional lymph nodes</subject><subject>Risk analysis</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>rRNA 18S</subject><subject>Small intestine</subject><subject>Survival</subject><subject>Tumor cells</subject><subject>Tumors</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kktvEzEQgFcIRB9w44xW4sKhgfF7fUGNQimVIqjK42p5_QiOdtfBzvL493ibUiVIHEa2xp8_z8hTVc8QvCJEwuuw7jMmIClj_EF1jCjGMwAuHu7tj6qTnNcAmGAmH1dHpLBYUnFcnV-nuBpi3gZTfwqrIfhg9GBcHX19eX3DWN3ffJjXF782yeUc4lCHoV7ErmwWE5eeVI-87rJ7ereeVl_eXXxevJ8tP15eLebLmWEN286Etc624BtjGLOGGi9Ma7UAaHFJtFY4ZChqDffUc08Am4Zy2hLtHWpaQU6rq53XRr1WmxR6nX6rqIO6TcS0UjqVLjqnmGy0lZQiSTQV0jXEMo-JFYIDJ1wW13Lnyj_dZmwPbN24KdGWULmoKNPGg1G61K4oEKGalmBlkGaOlEccTLrZf3Vvw9f5bXFjPyokKeGo8G92fIF7Z40btkl3B9cOT4bwTa3iDyURcGCkCF7eCVL8Prq8VX3IxnWdHlwcs8Kc0wYEJ7SgL_5B13FMQ_mpiSIgZCOmis52lEkx5-T8fTEI1DRlan_KCv58v4F7-O9YkT8FIczA</recordid><startdate>20220501</startdate><enddate>20220501</enddate><creator>Ismail, Hager Tarek H</creator><creator>AbdelMageed, Manar</creator><creator>Lindmark, Gudrun</creator><creator>Hammarström, Marie-Louise</creator><creator>Hammarström, Sten</creator><creator>Sitohy, Basel</creator><general>MDPI AG</general><general>MDPI</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>ADHXS</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>D93</scope><scope>ZZAVC</scope><scope>AGCHP</scope><scope>D95</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-8803-4798</orcidid><orcidid>https://orcid.org/0000-0003-3631-6122</orcidid><orcidid>https://orcid.org/0000-0002-4010-4002</orcidid><orcidid>https://orcid.org/0000-0001-9215-7758</orcidid></search><sort><creationdate>20220501</creationdate><title>Prognostic Significance of GPR55 mRNA Expression in Colon Cancer</title><author>Ismail, Hager Tarek H ; AbdelMageed, Manar ; Lindmark, Gudrun ; Hammarström, Marie-Louise ; Hammarström, Sten ; Sitohy, Basel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c585t-7ddedb0f8cc55dc4cf7cbda700b255dbd7e1c41bc6f4f6f302c8464b3afe18b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Basic Medicine</topic><topic>Biomarkers</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Cancer and Oncology</topic><topic>Cancer och onkologi</topic><topic>Carcinoembryonic Antigen - genetics</topic><topic>CEA</topic><topic>Cell and Molecular Biology</topic><topic>Cell- och molekylärbiologi</topic><topic>Clinical Medicine</topic><topic>Colon</topic><topic>Colon cancer</topic><topic>Colonic Neoplasms - genetics</topic><topic>Colonic Neoplasms - pathology</topic><topic>Colorectal cancer</topic><topic>CXCL16</topic><topic>CXCL16 protein</topic><topic>CXCL17</topic><topic>Gene expression</topic><topic>GPR55</topic><topic>Humans</topic><topic>Immune system</topic><topic>Immunosurveillance</topic><topic>Innate immunity</topic><topic>Klinisk medicin</topic><topic>Lymph nodes</topic><topic>Lymphatic system</topic><topic>Lymphocytes</topic><topic>Lymphocytes B</topic><topic>Lymphocytes T</topic><topic>Markers</topic><topic>Medical and Health Sciences</topic><topic>Medical prognosis</topic><topic>Medicin och hälsovetenskap</topic><topic>Medicinska och farmaceutiska grundvetenskaper</topic><topic>Patients</topic><topic>Prognosis</topic><topic>qRT-PCR</topic><topic>Receptors, Cannabinoid</topic><topic>regional lymph nodes</topic><topic>Risk analysis</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>rRNA 18S</topic><topic>Small intestine</topic><topic>Survival</topic><topic>Tumor cells</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ismail, Hager Tarek H</creatorcontrib><creatorcontrib>AbdelMageed, Manar</creatorcontrib><creatorcontrib>Lindmark, Gudrun</creatorcontrib><creatorcontrib>Hammarström, Marie-Louise</creatorcontrib><creatorcontrib>Hammarström, Sten</creatorcontrib><creatorcontrib>Sitohy, Basel</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>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Databases</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content 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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SWEPUB Umeå universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Umeå universitet</collection><collection>SwePub Articles full text</collection><collection>SWEPUB Lunds universitet full text</collection><collection>SWEPUB Lunds universitet</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ismail, Hager Tarek H</au><au>AbdelMageed, Manar</au><au>Lindmark, Gudrun</au><au>Hammarström, Marie-Louise</au><au>Hammarström, Sten</au><au>Sitohy, Basel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic Significance of GPR55 mRNA Expression in Colon Cancer</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2022-05-01</date><risdate>2022</risdate><volume>23</volume><issue>9</issue><spage>4556</spage><pages>4556-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>G protein-coupled receptor 55 (GPR55) probably plays a role in innate immunity and tumor immunosurveillance through its effect on immune cells, such as T cells and NK cells. In this study, the prognostic value of GPR55 in colon cancer (CC) was investigated. mRNA expression levels of GPR55 were determined in 382 regional lymph nodes of 121 CC patients with 12 years observation time after curative surgery. The same clinical material had previously been analyzed for expression levels of CEA, CXCL16, CXCL17, GPR35 V2/3 and LGR5 mRNAs. Clinical cutoffs of 0.1365 copies/18S rRNA unit for GPR55 and 0.1481 for the GPR55/CEA ratio were applied to differentiate between the high- and low-GPR55 expression groups. Kaplan-Meier survival analysis and Cox regression risk analysis were used to determine prognostic value. Improved discrimination between the two groups was achieved by combining GPR55 with CEA, CXCL16 or CXCL17 compared with GPR55 alone. The best result was obtained using the GPR55/CEA ratio, with an increased mean survival time of 14 and 33 months at 5 and 12 years observation time, respectively (
= 0.0003 and
= 0.003) for the high-GPR55/CEA group. The explanation for the observed improvement is most likely that GPR55 is a marker for T cells and B cells in lymph nodes, whereas CEA, CXCL16 and CXCL17, are markers for tumor cells of epithelial origin.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35562947</pmid><doi>10.3390/ijms23094556</doi><orcidid>https://orcid.org/0000-0001-8803-4798</orcidid><orcidid>https://orcid.org/0000-0003-3631-6122</orcidid><orcidid>https://orcid.org/0000-0002-4010-4002</orcidid><orcidid>https://orcid.org/0000-0001-9215-7758</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1422-0067 |
ispartof | International journal of molecular sciences, 2022-05, Vol.23 (9), p.4556 |
issn | 1422-0067 1661-6596 1422-0067 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_598ad944193a479e83d5f23d77606369 |
source | Publicly Available Content Database; PubMed Central |
subjects | Basic Medicine Biomarkers Biomarkers, Tumor - genetics Biomarkers, Tumor - metabolism Cancer and Oncology Cancer och onkologi Carcinoembryonic Antigen - genetics CEA Cell and Molecular Biology Cell- och molekylärbiologi Clinical Medicine Colon Colon cancer Colonic Neoplasms - genetics Colonic Neoplasms - pathology Colorectal cancer CXCL16 CXCL16 protein CXCL17 Gene expression GPR55 Humans Immune system Immunosurveillance Innate immunity Klinisk medicin Lymph nodes Lymphatic system Lymphocytes Lymphocytes B Lymphocytes T Markers Medical and Health Sciences Medical prognosis Medicin och hälsovetenskap Medicinska och farmaceutiska grundvetenskaper Patients Prognosis qRT-PCR Receptors, Cannabinoid regional lymph nodes Risk analysis RNA, Messenger - genetics RNA, Messenger - metabolism rRNA 18S Small intestine Survival Tumor cells Tumors |
title | Prognostic Significance of GPR55 mRNA Expression in Colon Cancer |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T22%3A27%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Prognostic%20Significance%20of%20GPR55%20mRNA%20Expression%20in%20Colon%20Cancer&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Ismail,%20Hager%20Tarek%20H&rft.date=2022-05-01&rft.volume=23&rft.issue=9&rft.spage=4556&rft.pages=4556-&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms23094556&rft_dat=%3Cproquest_doaj_%3E2664807634%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c585t-7ddedb0f8cc55dc4cf7cbda700b255dbd7e1c41bc6f4f6f302c8464b3afe18b73%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2663079871&rft_id=info:pmid/35562947&rfr_iscdi=true |