Loading…
High-Precision Quantitative Analysis Reveals Carcinoembryonic Protein Expression Differs Among Colorectal Cancer Primary Foci and Metastases to Different Sites
The expression of carcinoembryonic protein (CEA) is an important biological marker and therapeutic target in colorectal cancer (CRC). CEA expression heterogeneity confers resistance to CEA-targeting immunotherapy antibodies. Thus, quantification of the CEA-positive cell ratio among all tumor cells w...
Saved in:
Published in: | Technology in cancer research & treatment 2021, Vol.20, p.15330338211037175-15330338211037175 |
---|---|
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-c532t-99b04e20672d390d98fb32f6be7f4bb61b51f53382eeb55b0bf55fc6f9a62a9a3 |
---|---|
cites | cdi_FETCH-LOGICAL-c532t-99b04e20672d390d98fb32f6be7f4bb61b51f53382eeb55b0bf55fc6f9a62a9a3 |
container_end_page | 15330338211037175 |
container_issue | |
container_start_page | 15330338211037175 |
container_title | Technology in cancer research & treatment |
container_volume | 20 |
creator | Zhu, Yazhen Zhang, Qin Wei, Chengjiang Hu, Ying Gong, Han Liu, Yi Lai, Hao Feng, Yan Lin, Yuan |
description | The expression of carcinoembryonic protein (CEA) is an important biological marker and therapeutic target in colorectal cancer (CRC). CEA expression heterogeneity confers resistance to CEA-targeting immunotherapy antibodies. Thus, quantification of the CEA-positive cell ratio among all tumor cells would be important in identifying patients that would benefit from CEA-targeted therapies. However, the proportion of tumor cells that express CEA within primary and metastasized tumors at different sites has not been studied. Therefore, the present study aimed to determine CEA positive cell proportion in paired CRC primary foci, liver metastases, and lymph node (LN) metastases, and whether proportion of CEA positive cell differs among colorectal cancer primary foci, liver metastases, and LN metastases from 26 patients. The CEA expression was detected by immunohistochemical assay. Then we set up a quantification approach to quantify the proportion of CEA-positive cells based on the TissueGnostics (TG) system. Then the proportion of CEA positive cells were measured and compared among primary foci, liver metastases, and LN metastases. As a result, the proportion of CEA positive tumor cells was slightly higher in liver metastases than in primary foci (89.8% ± 2.71% vs 82.1% ± 5.05%, P < 0.001). The proportion of CEA-positive cells was significantly lower in LN metastases than in primary foci (82.3% ± 4.32% vs 70.28% ± 5.04%, P < 0.001). In 8 cases with matched CRC primary foci, liver metastases, and LN metastases, the proportions of CEA proportion in liver metastasis was the highest, followed by primary foci and LNs metastasis. In conclusion, this study provided an new approach for quantification of CEA positive cell in tumors and proved the percentage of CEA-positive cells varied in different metastases. |
doi_str_mv | 10.1177/15330338211037175 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_98bf74027cdf49ceab271b22badda30f</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_15330338211037175</sage_id><doaj_id>oai_doaj_org_article_98bf74027cdf49ceab271b22badda30f</doaj_id><sourcerecordid>2557547127</sourcerecordid><originalsourceid>FETCH-LOGICAL-c532t-99b04e20672d390d98fb32f6be7f4bb61b51f53382eeb55b0bf55fc6f9a62a9a3</originalsourceid><addsrcrecordid>eNp1kttuEzEQhleIipbCA3CDLHHDTYoP63X2BikKLa3UinK6tmzveOtoYwfbicjT8Ko43RAoCMmSrfH_fzNjT1W9IPiMECHeEM4YZmxKCcFMEMEfVSe72GQXfHw4181x9TSlBca0aRh5Uh2zmtWU1vyk-nHp-rvJbQTjkgsefVwrn11W2W0Azbwatskl9Ak2oIaE5ioa5wMsddwG7wy6jSGD8-j8-ypCuie8c9ZCTGi2DL5H8zCEAs9qKGZvIBaLW6q4RRfBOKR8h24gq1QWJJTD3g4-o88uQ3pWHdmSGZ7v99Pq68X5l_nl5PrD-6v57HpiOKN50rYa10BxI2jHWty1U6sZtY0GYWutG6I5sXz3VACac4215dyaxraqoapV7LS6GrldUAu5GmuUQTl5HwixlypmZwaQ7VRbUWMqTGfr1oDSVBBNqVZdpxi2hfV2ZK3WegmdKc1ENTyAPrzx7k72YSOnjBNM6wJ4vQfE8G0NKculSwaGQXkI6yQp54LXglBRpK_-ki7COpZ_K6qGMNryhu2AZFSZGFKKYA_FECx3oyT_GaXieflnFwfHr9kpgrNRkFQPv9P-n_gTZXLU4A</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2613295634</pqid></control><display><type>article</type><title>High-Precision Quantitative Analysis Reveals Carcinoembryonic Protein Expression Differs Among Colorectal Cancer Primary Foci and Metastases to Different Sites</title><source>Open Access: PubMed Central</source><source>Publicly Available Content Database</source><source>Sage Journals GOLD Open Access 2024</source><creator>Zhu, Yazhen ; Zhang, Qin ; Wei, Chengjiang ; Hu, Ying ; Gong, Han ; Liu, Yi ; Lai, Hao ; Feng, Yan ; Lin, Yuan</creator><creatorcontrib>Zhu, Yazhen ; Zhang, Qin ; Wei, Chengjiang ; Hu, Ying ; Gong, Han ; Liu, Yi ; Lai, Hao ; Feng, Yan ; Lin, Yuan</creatorcontrib><description>The expression of carcinoembryonic protein (CEA) is an important biological marker and therapeutic target in colorectal cancer (CRC). CEA expression heterogeneity confers resistance to CEA-targeting immunotherapy antibodies. Thus, quantification of the CEA-positive cell ratio among all tumor cells would be important in identifying patients that would benefit from CEA-targeted therapies. However, the proportion of tumor cells that express CEA within primary and metastasized tumors at different sites has not been studied. Therefore, the present study aimed to determine CEA positive cell proportion in paired CRC primary foci, liver metastases, and lymph node (LN) metastases, and whether proportion of CEA positive cell differs among colorectal cancer primary foci, liver metastases, and LN metastases from 26 patients. The CEA expression was detected by immunohistochemical assay. Then we set up a quantification approach to quantify the proportion of CEA-positive cells based on the TissueGnostics (TG) system. Then the proportion of CEA positive cells were measured and compared among primary foci, liver metastases, and LN metastases. As a result, the proportion of CEA positive tumor cells was slightly higher in liver metastases than in primary foci (89.8% ± 2.71% vs 82.1% ± 5.05%, P < 0.001). The proportion of CEA-positive cells was significantly lower in LN metastases than in primary foci (82.3% ± 4.32% vs 70.28% ± 5.04%, P < 0.001). In 8 cases with matched CRC primary foci, liver metastases, and LN metastases, the proportions of CEA proportion in liver metastasis was the highest, followed by primary foci and LNs metastasis. In conclusion, this study provided an new approach for quantification of CEA positive cell in tumors and proved the percentage of CEA-positive cells varied in different metastases.</description><identifier>ISSN: 1533-0346</identifier><identifier>EISSN: 1533-0338</identifier><identifier>DOI: 10.1177/15330338211037175</identifier><identifier>PMID: 34342245</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Adenocarcinoma - metabolism ; Adenocarcinoma - secondary ; Adult ; Aged ; Carcinoembryonic Antigen - metabolism ; Colorectal cancer ; Colorectal carcinoma ; Colorectal Neoplasms - metabolism ; Colorectal Neoplasms - pathology ; Female ; Humans ; Immunohistochemistry ; Immunotherapy ; Liver ; Liver cancer ; Liver Neoplasms - metabolism ; Liver Neoplasms - secondary ; Lymph nodes ; Lymph Nodes - metabolism ; Lymphatic Metastasis ; Male ; Metastases ; Metastasis ; Middle Aged ; Original ; Quantitative analysis ; Therapeutic targets ; Tumor cells ; Tumors</subject><ispartof>Technology in cancer research & treatment, 2021, Vol.20, p.15330338211037175-15330338211037175</ispartof><rights>The Author(s) 2021</rights><rights>The Author(s) 2021. This work is licensed under the Creative Commons Attribution – Non-Commercial License https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2021 2021 SAGE Publications</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c532t-99b04e20672d390d98fb32f6be7f4bb61b51f53382eeb55b0bf55fc6f9a62a9a3</citedby><cites>FETCH-LOGICAL-c532t-99b04e20672d390d98fb32f6be7f4bb61b51f53382eeb55b0bf55fc6f9a62a9a3</cites><orcidid>0000-0002-3906-6539</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/PMC8351024/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2613295634?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,4024,21966,25753,27853,27923,27924,27925,37012,37013,44590,44945,45333,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34342245$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhu, Yazhen</creatorcontrib><creatorcontrib>Zhang, Qin</creatorcontrib><creatorcontrib>Wei, Chengjiang</creatorcontrib><creatorcontrib>Hu, Ying</creatorcontrib><creatorcontrib>Gong, Han</creatorcontrib><creatorcontrib>Liu, Yi</creatorcontrib><creatorcontrib>Lai, Hao</creatorcontrib><creatorcontrib>Feng, Yan</creatorcontrib><creatorcontrib>Lin, Yuan</creatorcontrib><title>High-Precision Quantitative Analysis Reveals Carcinoembryonic Protein Expression Differs Among Colorectal Cancer Primary Foci and Metastases to Different Sites</title><title>Technology in cancer research & treatment</title><addtitle>Technol Cancer Res Treat</addtitle><description>The expression of carcinoembryonic protein (CEA) is an important biological marker and therapeutic target in colorectal cancer (CRC). CEA expression heterogeneity confers resistance to CEA-targeting immunotherapy antibodies. Thus, quantification of the CEA-positive cell ratio among all tumor cells would be important in identifying patients that would benefit from CEA-targeted therapies. However, the proportion of tumor cells that express CEA within primary and metastasized tumors at different sites has not been studied. Therefore, the present study aimed to determine CEA positive cell proportion in paired CRC primary foci, liver metastases, and lymph node (LN) metastases, and whether proportion of CEA positive cell differs among colorectal cancer primary foci, liver metastases, and LN metastases from 26 patients. The CEA expression was detected by immunohistochemical assay. Then we set up a quantification approach to quantify the proportion of CEA-positive cells based on the TissueGnostics (TG) system. Then the proportion of CEA positive cells were measured and compared among primary foci, liver metastases, and LN metastases. As a result, the proportion of CEA positive tumor cells was slightly higher in liver metastases than in primary foci (89.8% ± 2.71% vs 82.1% ± 5.05%, P < 0.001). The proportion of CEA-positive cells was significantly lower in LN metastases than in primary foci (82.3% ± 4.32% vs 70.28% ± 5.04%, P < 0.001). In 8 cases with matched CRC primary foci, liver metastases, and LN metastases, the proportions of CEA proportion in liver metastasis was the highest, followed by primary foci and LNs metastasis. In conclusion, this study provided an new approach for quantification of CEA positive cell in tumors and proved the percentage of CEA-positive cells varied in different metastases.</description><subject>Adenocarcinoma - metabolism</subject><subject>Adenocarcinoma - secondary</subject><subject>Adult</subject><subject>Aged</subject><subject>Carcinoembryonic Antigen - metabolism</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Immunotherapy</subject><subject>Liver</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - metabolism</subject><subject>Liver Neoplasms - secondary</subject><subject>Lymph nodes</subject><subject>Lymph Nodes - metabolism</subject><subject>Lymphatic Metastasis</subject><subject>Male</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Quantitative analysis</subject><subject>Therapeutic targets</subject><subject>Tumor cells</subject><subject>Tumors</subject><issn>1533-0346</issn><issn>1533-0338</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kttuEzEQhleIipbCA3CDLHHDTYoP63X2BikKLa3UinK6tmzveOtoYwfbicjT8Ko43RAoCMmSrfH_fzNjT1W9IPiMECHeEM4YZmxKCcFMEMEfVSe72GQXfHw4181x9TSlBca0aRh5Uh2zmtWU1vyk-nHp-rvJbQTjkgsefVwrn11W2W0Azbwatskl9Ak2oIaE5ioa5wMsddwG7wy6jSGD8-j8-ypCuie8c9ZCTGi2DL5H8zCEAs9qKGZvIBaLW6q4RRfBOKR8h24gq1QWJJTD3g4-o88uQ3pWHdmSGZ7v99Pq68X5l_nl5PrD-6v57HpiOKN50rYa10BxI2jHWty1U6sZtY0GYWutG6I5sXz3VACac4215dyaxraqoapV7LS6GrldUAu5GmuUQTl5HwixlypmZwaQ7VRbUWMqTGfr1oDSVBBNqVZdpxi2hfV2ZK3WegmdKc1ENTyAPrzx7k72YSOnjBNM6wJ4vQfE8G0NKculSwaGQXkI6yQp54LXglBRpK_-ki7COpZ_K6qGMNryhu2AZFSZGFKKYA_FECx3oyT_GaXieflnFwfHr9kpgrNRkFQPv9P-n_gTZXLU4A</recordid><startdate>2021</startdate><enddate>2021</enddate><creator>Zhu, Yazhen</creator><creator>Zhang, Qin</creator><creator>Wei, Chengjiang</creator><creator>Hu, Ying</creator><creator>Gong, Han</creator><creator>Liu, Yi</creator><creator>Lai, Hao</creator><creator>Feng, Yan</creator><creator>Lin, Yuan</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><general>SAGE Publishing</general><scope>AFRWT</scope><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>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</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>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3906-6539</orcidid></search><sort><creationdate>2021</creationdate><title>High-Precision Quantitative Analysis Reveals Carcinoembryonic Protein Expression Differs Among Colorectal Cancer Primary Foci and Metastases to Different Sites</title><author>Zhu, Yazhen ; Zhang, Qin ; Wei, Chengjiang ; Hu, Ying ; Gong, Han ; Liu, Yi ; Lai, Hao ; Feng, Yan ; Lin, Yuan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c532t-99b04e20672d390d98fb32f6be7f4bb61b51f53382eeb55b0bf55fc6f9a62a9a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adenocarcinoma - metabolism</topic><topic>Adenocarcinoma - secondary</topic><topic>Adult</topic><topic>Aged</topic><topic>Carcinoembryonic Antigen - metabolism</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Immunotherapy</topic><topic>Liver</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - metabolism</topic><topic>Liver Neoplasms - secondary</topic><topic>Lymph nodes</topic><topic>Lymph Nodes - metabolism</topic><topic>Lymphatic Metastasis</topic><topic>Male</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Quantitative analysis</topic><topic>Therapeutic targets</topic><topic>Tumor cells</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhu, Yazhen</creatorcontrib><creatorcontrib>Zhang, Qin</creatorcontrib><creatorcontrib>Wei, Chengjiang</creatorcontrib><creatorcontrib>Hu, Ying</creatorcontrib><creatorcontrib>Gong, Han</creatorcontrib><creatorcontrib>Liu, Yi</creatorcontrib><creatorcontrib>Lai, Hao</creatorcontrib><creatorcontrib>Feng, Yan</creatorcontrib><creatorcontrib>Lin, Yuan</creatorcontrib><collection>Sage Journals GOLD Open Access 2024</collection><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>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</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>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</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>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Technology in cancer research & treatment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhu, Yazhen</au><au>Zhang, Qin</au><au>Wei, Chengjiang</au><au>Hu, Ying</au><au>Gong, Han</au><au>Liu, Yi</au><au>Lai, Hao</au><au>Feng, Yan</au><au>Lin, Yuan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-Precision Quantitative Analysis Reveals Carcinoembryonic Protein Expression Differs Among Colorectal Cancer Primary Foci and Metastases to Different Sites</atitle><jtitle>Technology in cancer research & treatment</jtitle><addtitle>Technol Cancer Res Treat</addtitle><date>2021</date><risdate>2021</risdate><volume>20</volume><spage>15330338211037175</spage><epage>15330338211037175</epage><pages>15330338211037175-15330338211037175</pages><issn>1533-0346</issn><eissn>1533-0338</eissn><abstract>The expression of carcinoembryonic protein (CEA) is an important biological marker and therapeutic target in colorectal cancer (CRC). CEA expression heterogeneity confers resistance to CEA-targeting immunotherapy antibodies. Thus, quantification of the CEA-positive cell ratio among all tumor cells would be important in identifying patients that would benefit from CEA-targeted therapies. However, the proportion of tumor cells that express CEA within primary and metastasized tumors at different sites has not been studied. Therefore, the present study aimed to determine CEA positive cell proportion in paired CRC primary foci, liver metastases, and lymph node (LN) metastases, and whether proportion of CEA positive cell differs among colorectal cancer primary foci, liver metastases, and LN metastases from 26 patients. The CEA expression was detected by immunohistochemical assay. Then we set up a quantification approach to quantify the proportion of CEA-positive cells based on the TissueGnostics (TG) system. Then the proportion of CEA positive cells were measured and compared among primary foci, liver metastases, and LN metastases. As a result, the proportion of CEA positive tumor cells was slightly higher in liver metastases than in primary foci (89.8% ± 2.71% vs 82.1% ± 5.05%, P < 0.001). The proportion of CEA-positive cells was significantly lower in LN metastases than in primary foci (82.3% ± 4.32% vs 70.28% ± 5.04%, P < 0.001). In 8 cases with matched CRC primary foci, liver metastases, and LN metastases, the proportions of CEA proportion in liver metastasis was the highest, followed by primary foci and LNs metastasis. In conclusion, this study provided an new approach for quantification of CEA positive cell in tumors and proved the percentage of CEA-positive cells varied in different metastases.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>34342245</pmid><doi>10.1177/15330338211037175</doi><orcidid>https://orcid.org/0000-0002-3906-6539</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1533-0346 |
ispartof | Technology in cancer research & treatment, 2021, Vol.20, p.15330338211037175-15330338211037175 |
issn | 1533-0346 1533-0338 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_98bf74027cdf49ceab271b22badda30f |
source | Open Access: PubMed Central; Publicly Available Content Database; Sage Journals GOLD Open Access 2024 |
subjects | Adenocarcinoma - metabolism Adenocarcinoma - secondary Adult Aged Carcinoembryonic Antigen - metabolism Colorectal cancer Colorectal carcinoma Colorectal Neoplasms - metabolism Colorectal Neoplasms - pathology Female Humans Immunohistochemistry Immunotherapy Liver Liver cancer Liver Neoplasms - metabolism Liver Neoplasms - secondary Lymph nodes Lymph Nodes - metabolism Lymphatic Metastasis Male Metastases Metastasis Middle Aged Original Quantitative analysis Therapeutic targets Tumor cells Tumors |
title | High-Precision Quantitative Analysis Reveals Carcinoembryonic Protein Expression Differs Among Colorectal Cancer Primary Foci and Metastases to Different Sites |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T05%3A32%3A40IST&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=High-Precision%20Quantitative%20Analysis%20Reveals%20Carcinoembryonic%20Protein%20Expression%20Differs%20Among%20Colorectal%20Cancer%20Primary%20Foci%20and%20Metastases%20to%20Different%20Sites&rft.jtitle=Technology%20in%20cancer%20research%20&%20treatment&rft.au=Zhu,%20Yazhen&rft.date=2021&rft.volume=20&rft.spage=15330338211037175&rft.epage=15330338211037175&rft.pages=15330338211037175-15330338211037175&rft.issn=1533-0346&rft.eissn=1533-0338&rft_id=info:doi/10.1177/15330338211037175&rft_dat=%3Cproquest_doaj_%3E2557547127%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c532t-99b04e20672d390d98fb32f6be7f4bb61b51f53382eeb55b0bf55fc6f9a62a9a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2613295634&rft_id=info:pmid/34342245&rft_sage_id=10.1177_15330338211037175&rfr_iscdi=true |