Vaccination with human amniotic epithelial cells confer effective protection in a murine model of Colon adenocarcinoma

As a prophylactic cancer vaccine, human amniotic membrane epithelial cells (hAECs) conferred effective protection in a murine model of colon cancer. The immunized mice mounted strong cross‐protective CTL and antibody responses. Tumor burden was significantly reduced in tumor‐bearing mice after immun...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of cancer 2018-04, Vol.142 (7), p.1453-1466
Hauptverfasser: Tabatabaei, M., Mosaffa, N., Ghods, R., Nikoo, S., Kazemnejad, S., Khanmohammadi, M., Mirzadeghan, E., Mahmoudi, A.R., Bolouri, M.R., Falak, R., Keshavarzi, B., Ramezani, M., Zarnani, A.H.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1466
container_issue 7
container_start_page 1453
container_title International journal of cancer
container_volume 142
creator Tabatabaei, M.
Mosaffa, N.
Ghods, R.
Nikoo, S.
Kazemnejad, S.
Khanmohammadi, M.
Mirzadeghan, E.
Mahmoudi, A.R.
Bolouri, M.R.
Falak, R.
Keshavarzi, B.
Ramezani, M.
Zarnani, A.H.
description As a prophylactic cancer vaccine, human amniotic membrane epithelial cells (hAECs) conferred effective protection in a murine model of colon cancer. The immunized mice mounted strong cross‐protective CTL and antibody responses. Tumor burden was significantly reduced in tumor‐bearing mice after immunization with hAECs. Placental cancer immunotherapy could be a promising approach for primary prevention of cancer. In spite of being the star of therapeutic strategies for cancer treatment, the results of immunotherapeutic approaches are still far from expectations. In this regard, primary prevention of cancer using prophylactic cancer vaccines has gained considerable attention. The immunologic similarities between cancer development and placentation have helped researchers to unravel molecular mechanisms responsible for carcinogenesis and to take advantage of stem cells from reproductive organs to elicit robust anti‐cancer immune responses. Here, we showed that vaccination of mice with human amniotic membrane epithelial cells (hAECs) conferred effective protection against colon cancer and led to expansion of systemic and splenic cytotoxic T cell population and induction of cross‐protective cytotoxic responses against tumor cells. Vaccinated mice mounted tumor‐specific Th1 responses and produced cross‐reactive antibodies against cell surface markers of cancer cells. Tumor burden was also significantly reduced in tumor‐bearing mice immunized with hAECs. Our findings pave the way for potential future application of hAECs as an effective prophylactic cancer vaccine. What's new? Cancer stem cells are immunologically similar to embryonic stem cells (ESCs). In particular, both express antigens that are elevated in the presence of cancer. Ethical issues surrounding the use of ESCs have motivated the search for additional cell types with similar stem properties. Our study shows, in a murine model of colon cancer, that placenta‐derived human amniotic membrane epithelial cells (hAECs) can elicit a strong anticancer immune response, effectively protecting animals against colon tumor development. In mice with tumors, hAEC treatment lessened tumor burden significantly. The findings suggest that placental cancer immunotherapy is a promising approach for cancer prevention.
doi_str_mv 10.1002/ijc.31159
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1999047124</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1999047124</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3889-620d879be207c691316b773540e3d942de2a6bf84091fcc61b4caac69baadbe03</originalsourceid><addsrcrecordid>eNp1kD1PwzAQhi0EoqUw8AeQJSaGtLaTJvGIKj6KKrEAq-U4Z9WVYxcnoeq_xyWFjckn33PPnV6ErimZUkLYzGzUNKV0zk_QmBJeJITR-Skaxx5JCprmI3TRthtCIkOyczRinKacMjZGXx9SKeNkZ7zDO9Ot8bpvpMOyccZ3RmHYxk-wRlqswNoWK-80BAxag-rMF-Bt8N2hjAITB3HTB-MAN74Gi73GC29jS9bgvJIhLvONvERnWtoWro7vBL0_PrwtnpPV69Nycb9KVFqWPMkZqcuCV8BIofJ4NM2rokjnGYG05hmrgcm80mVGONVK5bTKlJSRrKSsKyDpBN0O3njkZw9tJza-Dy6uFJRzTrKCsixSdwOlgm_bAFpsg2lk2AtKxCFhERMWPwlH9uZo7KsG6j_yN9IIzAZgZyzs_zeJ5ctiUH4DicyGkw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1999047124</pqid></control><display><type>article</type><title>Vaccination with human amniotic epithelial cells confer effective protection in a murine model of Colon adenocarcinoma</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Wiley Online Library All Journals</source><creator>Tabatabaei, M. ; Mosaffa, N. ; Ghods, R. ; Nikoo, S. ; Kazemnejad, S. ; Khanmohammadi, M. ; Mirzadeghan, E. ; Mahmoudi, A.R. ; Bolouri, M.R. ; Falak, R. ; Keshavarzi, B. ; Ramezani, M. ; Zarnani, A.H.</creator><creatorcontrib>Tabatabaei, M. ; Mosaffa, N. ; Ghods, R. ; Nikoo, S. ; Kazemnejad, S. ; Khanmohammadi, M. ; Mirzadeghan, E. ; Mahmoudi, A.R. ; Bolouri, M.R. ; Falak, R. ; Keshavarzi, B. ; Ramezani, M. ; Zarnani, A.H.</creatorcontrib><description>As a prophylactic cancer vaccine, human amniotic membrane epithelial cells (hAECs) conferred effective protection in a murine model of colon cancer. The immunized mice mounted strong cross‐protective CTL and antibody responses. Tumor burden was significantly reduced in tumor‐bearing mice after immunization with hAECs. Placental cancer immunotherapy could be a promising approach for primary prevention of cancer. In spite of being the star of therapeutic strategies for cancer treatment, the results of immunotherapeutic approaches are still far from expectations. In this regard, primary prevention of cancer using prophylactic cancer vaccines has gained considerable attention. The immunologic similarities between cancer development and placentation have helped researchers to unravel molecular mechanisms responsible for carcinogenesis and to take advantage of stem cells from reproductive organs to elicit robust anti‐cancer immune responses. Here, we showed that vaccination of mice with human amniotic membrane epithelial cells (hAECs) conferred effective protection against colon cancer and led to expansion of systemic and splenic cytotoxic T cell population and induction of cross‐protective cytotoxic responses against tumor cells. Vaccinated mice mounted tumor‐specific Th1 responses and produced cross‐reactive antibodies against cell surface markers of cancer cells. Tumor burden was also significantly reduced in tumor‐bearing mice immunized with hAECs. Our findings pave the way for potential future application of hAECs as an effective prophylactic cancer vaccine. What's new? Cancer stem cells are immunologically similar to embryonic stem cells (ESCs). In particular, both express antigens that are elevated in the presence of cancer. Ethical issues surrounding the use of ESCs have motivated the search for additional cell types with similar stem properties. Our study shows, in a murine model of colon cancer, that placenta‐derived human amniotic membrane epithelial cells (hAECs) can elicit a strong anticancer immune response, effectively protecting animals against colon tumor development. In mice with tumors, hAEC treatment lessened tumor burden significantly. The findings suggest that placental cancer immunotherapy is a promising approach for cancer prevention.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.31159</identifier><identifier>PMID: 29139122</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Adenocarcinoma ; Adenocarcinoma - immunology ; Adenocarcinoma - pathology ; Amnion ; Amniotic membrane ; Animal models ; Animals ; Antigens ; anti‐tumor immunity ; Cancer ; Cancer immunotherapy ; cancer vaccine ; Cancer vaccines ; Cancer Vaccines - pharmacology ; Carcinogenesis ; Cell surface ; Colon cancer ; Colonic Neoplasms - immunology ; Colonic Neoplasms - pathology ; Colorectal cancer ; Cytotoxicity ; Disease Models, Animal ; Embryo cells ; Epithelial Cells ; Ethical standards ; Ethics ; Female ; human amniotic epithelial cells ; Humans ; Immune response ; Immunotherapy ; Lymphocytes T ; Medical research ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Molecular modelling ; Organs ; Placenta ; prophylaxis ; Reproductive organs ; Spleen ; Stem cells ; Surface markers ; Tumor cells ; Tumors ; Vaccination ; Vaccines</subject><ispartof>International journal of cancer, 2018-04, Vol.142 (7), p.1453-1466</ispartof><rights>2017 UICC</rights><rights>2017 UICC.</rights><rights>2018 UICC</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3889-620d879be207c691316b773540e3d942de2a6bf84091fcc61b4caac69baadbe03</citedby><cites>FETCH-LOGICAL-c3889-620d879be207c691316b773540e3d942de2a6bf84091fcc61b4caac69baadbe03</cites><orcidid>0000-0003-4503-299X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.31159$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.31159$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29139122$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tabatabaei, M.</creatorcontrib><creatorcontrib>Mosaffa, N.</creatorcontrib><creatorcontrib>Ghods, R.</creatorcontrib><creatorcontrib>Nikoo, S.</creatorcontrib><creatorcontrib>Kazemnejad, S.</creatorcontrib><creatorcontrib>Khanmohammadi, M.</creatorcontrib><creatorcontrib>Mirzadeghan, E.</creatorcontrib><creatorcontrib>Mahmoudi, A.R.</creatorcontrib><creatorcontrib>Bolouri, M.R.</creatorcontrib><creatorcontrib>Falak, R.</creatorcontrib><creatorcontrib>Keshavarzi, B.</creatorcontrib><creatorcontrib>Ramezani, M.</creatorcontrib><creatorcontrib>Zarnani, A.H.</creatorcontrib><title>Vaccination with human amniotic epithelial cells confer effective protection in a murine model of Colon adenocarcinoma</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>As a prophylactic cancer vaccine, human amniotic membrane epithelial cells (hAECs) conferred effective protection in a murine model of colon cancer. The immunized mice mounted strong cross‐protective CTL and antibody responses. Tumor burden was significantly reduced in tumor‐bearing mice after immunization with hAECs. Placental cancer immunotherapy could be a promising approach for primary prevention of cancer. In spite of being the star of therapeutic strategies for cancer treatment, the results of immunotherapeutic approaches are still far from expectations. In this regard, primary prevention of cancer using prophylactic cancer vaccines has gained considerable attention. The immunologic similarities between cancer development and placentation have helped researchers to unravel molecular mechanisms responsible for carcinogenesis and to take advantage of stem cells from reproductive organs to elicit robust anti‐cancer immune responses. Here, we showed that vaccination of mice with human amniotic membrane epithelial cells (hAECs) conferred effective protection against colon cancer and led to expansion of systemic and splenic cytotoxic T cell population and induction of cross‐protective cytotoxic responses against tumor cells. Vaccinated mice mounted tumor‐specific Th1 responses and produced cross‐reactive antibodies against cell surface markers of cancer cells. Tumor burden was also significantly reduced in tumor‐bearing mice immunized with hAECs. Our findings pave the way for potential future application of hAECs as an effective prophylactic cancer vaccine. What's new? Cancer stem cells are immunologically similar to embryonic stem cells (ESCs). In particular, both express antigens that are elevated in the presence of cancer. Ethical issues surrounding the use of ESCs have motivated the search for additional cell types with similar stem properties. Our study shows, in a murine model of colon cancer, that placenta‐derived human amniotic membrane epithelial cells (hAECs) can elicit a strong anticancer immune response, effectively protecting animals against colon tumor development. In mice with tumors, hAEC treatment lessened tumor burden significantly. The findings suggest that placental cancer immunotherapy is a promising approach for cancer prevention.</description><subject>Adenocarcinoma</subject><subject>Adenocarcinoma - immunology</subject><subject>Adenocarcinoma - pathology</subject><subject>Amnion</subject><subject>Amniotic membrane</subject><subject>Animal models</subject><subject>Animals</subject><subject>Antigens</subject><subject>anti‐tumor immunity</subject><subject>Cancer</subject><subject>Cancer immunotherapy</subject><subject>cancer vaccine</subject><subject>Cancer vaccines</subject><subject>Cancer Vaccines - pharmacology</subject><subject>Carcinogenesis</subject><subject>Cell surface</subject><subject>Colon cancer</subject><subject>Colonic Neoplasms - immunology</subject><subject>Colonic Neoplasms - pathology</subject><subject>Colorectal cancer</subject><subject>Cytotoxicity</subject><subject>Disease Models, Animal</subject><subject>Embryo cells</subject><subject>Epithelial Cells</subject><subject>Ethical standards</subject><subject>Ethics</subject><subject>Female</subject><subject>human amniotic epithelial cells</subject><subject>Humans</subject><subject>Immune response</subject><subject>Immunotherapy</subject><subject>Lymphocytes T</subject><subject>Medical research</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Molecular modelling</subject><subject>Organs</subject><subject>Placenta</subject><subject>prophylaxis</subject><subject>Reproductive organs</subject><subject>Spleen</subject><subject>Stem cells</subject><subject>Surface markers</subject><subject>Tumor cells</subject><subject>Tumors</subject><subject>Vaccination</subject><subject>Vaccines</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kD1PwzAQhi0EoqUw8AeQJSaGtLaTJvGIKj6KKrEAq-U4Z9WVYxcnoeq_xyWFjckn33PPnV6ErimZUkLYzGzUNKV0zk_QmBJeJITR-Skaxx5JCprmI3TRthtCIkOyczRinKacMjZGXx9SKeNkZ7zDO9Ot8bpvpMOyccZ3RmHYxk-wRlqswNoWK-80BAxag-rMF-Bt8N2hjAITB3HTB-MAN74Gi73GC29jS9bgvJIhLvONvERnWtoWro7vBL0_PrwtnpPV69Nycb9KVFqWPMkZqcuCV8BIofJ4NM2rokjnGYG05hmrgcm80mVGONVK5bTKlJSRrKSsKyDpBN0O3njkZw9tJza-Dy6uFJRzTrKCsixSdwOlgm_bAFpsg2lk2AtKxCFhERMWPwlH9uZo7KsG6j_yN9IIzAZgZyzs_zeJ5ctiUH4DicyGkw</recordid><startdate>20180401</startdate><enddate>20180401</enddate><creator>Tabatabaei, M.</creator><creator>Mosaffa, N.</creator><creator>Ghods, R.</creator><creator>Nikoo, S.</creator><creator>Kazemnejad, S.</creator><creator>Khanmohammadi, M.</creator><creator>Mirzadeghan, E.</creator><creator>Mahmoudi, A.R.</creator><creator>Bolouri, M.R.</creator><creator>Falak, R.</creator><creator>Keshavarzi, B.</creator><creator>Ramezani, M.</creator><creator>Zarnani, A.H.</creator><general>Wiley Subscription Services, Inc</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>7T5</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><orcidid>https://orcid.org/0000-0003-4503-299X</orcidid></search><sort><creationdate>20180401</creationdate><title>Vaccination with human amniotic epithelial cells confer effective protection in a murine model of Colon adenocarcinoma</title><author>Tabatabaei, M. ; Mosaffa, N. ; Ghods, R. ; Nikoo, S. ; Kazemnejad, S. ; Khanmohammadi, M. ; Mirzadeghan, E. ; Mahmoudi, A.R. ; Bolouri, M.R. ; Falak, R. ; Keshavarzi, B. ; Ramezani, M. ; Zarnani, A.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3889-620d879be207c691316b773540e3d942de2a6bf84091fcc61b4caac69baadbe03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Adenocarcinoma</topic><topic>Adenocarcinoma - immunology</topic><topic>Adenocarcinoma - pathology</topic><topic>Amnion</topic><topic>Amniotic membrane</topic><topic>Animal models</topic><topic>Animals</topic><topic>Antigens</topic><topic>anti‐tumor immunity</topic><topic>Cancer</topic><topic>Cancer immunotherapy</topic><topic>cancer vaccine</topic><topic>Cancer vaccines</topic><topic>Cancer Vaccines - pharmacology</topic><topic>Carcinogenesis</topic><topic>Cell surface</topic><topic>Colon cancer</topic><topic>Colonic Neoplasms - immunology</topic><topic>Colonic Neoplasms - pathology</topic><topic>Colorectal cancer</topic><topic>Cytotoxicity</topic><topic>Disease Models, Animal</topic><topic>Embryo cells</topic><topic>Epithelial Cells</topic><topic>Ethical standards</topic><topic>Ethics</topic><topic>Female</topic><topic>human amniotic epithelial cells</topic><topic>Humans</topic><topic>Immune response</topic><topic>Immunotherapy</topic><topic>Lymphocytes T</topic><topic>Medical research</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Molecular modelling</topic><topic>Organs</topic><topic>Placenta</topic><topic>prophylaxis</topic><topic>Reproductive organs</topic><topic>Spleen</topic><topic>Stem cells</topic><topic>Surface markers</topic><topic>Tumor cells</topic><topic>Tumors</topic><topic>Vaccination</topic><topic>Vaccines</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tabatabaei, M.</creatorcontrib><creatorcontrib>Mosaffa, N.</creatorcontrib><creatorcontrib>Ghods, R.</creatorcontrib><creatorcontrib>Nikoo, S.</creatorcontrib><creatorcontrib>Kazemnejad, S.</creatorcontrib><creatorcontrib>Khanmohammadi, M.</creatorcontrib><creatorcontrib>Mirzadeghan, E.</creatorcontrib><creatorcontrib>Mahmoudi, A.R.</creatorcontrib><creatorcontrib>Bolouri, M.R.</creatorcontrib><creatorcontrib>Falak, R.</creatorcontrib><creatorcontrib>Keshavarzi, B.</creatorcontrib><creatorcontrib>Ramezani, M.</creatorcontrib><creatorcontrib>Zarnani, A.H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tabatabaei, M.</au><au>Mosaffa, N.</au><au>Ghods, R.</au><au>Nikoo, S.</au><au>Kazemnejad, S.</au><au>Khanmohammadi, M.</au><au>Mirzadeghan, E.</au><au>Mahmoudi, A.R.</au><au>Bolouri, M.R.</au><au>Falak, R.</au><au>Keshavarzi, B.</au><au>Ramezani, M.</au><au>Zarnani, A.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Vaccination with human amniotic epithelial cells confer effective protection in a murine model of Colon adenocarcinoma</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2018-04-01</date><risdate>2018</risdate><volume>142</volume><issue>7</issue><spage>1453</spage><epage>1466</epage><pages>1453-1466</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><abstract>As a prophylactic cancer vaccine, human amniotic membrane epithelial cells (hAECs) conferred effective protection in a murine model of colon cancer. The immunized mice mounted strong cross‐protective CTL and antibody responses. Tumor burden was significantly reduced in tumor‐bearing mice after immunization with hAECs. Placental cancer immunotherapy could be a promising approach for primary prevention of cancer. In spite of being the star of therapeutic strategies for cancer treatment, the results of immunotherapeutic approaches are still far from expectations. In this regard, primary prevention of cancer using prophylactic cancer vaccines has gained considerable attention. The immunologic similarities between cancer development and placentation have helped researchers to unravel molecular mechanisms responsible for carcinogenesis and to take advantage of stem cells from reproductive organs to elicit robust anti‐cancer immune responses. Here, we showed that vaccination of mice with human amniotic membrane epithelial cells (hAECs) conferred effective protection against colon cancer and led to expansion of systemic and splenic cytotoxic T cell population and induction of cross‐protective cytotoxic responses against tumor cells. Vaccinated mice mounted tumor‐specific Th1 responses and produced cross‐reactive antibodies against cell surface markers of cancer cells. Tumor burden was also significantly reduced in tumor‐bearing mice immunized with hAECs. Our findings pave the way for potential future application of hAECs as an effective prophylactic cancer vaccine. What's new? Cancer stem cells are immunologically similar to embryonic stem cells (ESCs). In particular, both express antigens that are elevated in the presence of cancer. Ethical issues surrounding the use of ESCs have motivated the search for additional cell types with similar stem properties. Our study shows, in a murine model of colon cancer, that placenta‐derived human amniotic membrane epithelial cells (hAECs) can elicit a strong anticancer immune response, effectively protecting animals against colon tumor development. In mice with tumors, hAEC treatment lessened tumor burden significantly. The findings suggest that placental cancer immunotherapy is a promising approach for cancer prevention.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29139122</pmid><doi>10.1002/ijc.31159</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-4503-299X</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0020-7136
ispartof International journal of cancer, 2018-04, Vol.142 (7), p.1453-1466
issn 0020-7136
1097-0215
language eng
recordid cdi_proquest_journals_1999047124
source MEDLINE; EZB-FREE-00999 freely available EZB journals; Wiley Online Library All Journals
subjects Adenocarcinoma
Adenocarcinoma - immunology
Adenocarcinoma - pathology
Amnion
Amniotic membrane
Animal models
Animals
Antigens
anti‐tumor immunity
Cancer
Cancer immunotherapy
cancer vaccine
Cancer vaccines
Cancer Vaccines - pharmacology
Carcinogenesis
Cell surface
Colon cancer
Colonic Neoplasms - immunology
Colonic Neoplasms - pathology
Colorectal cancer
Cytotoxicity
Disease Models, Animal
Embryo cells
Epithelial Cells
Ethical standards
Ethics
Female
human amniotic epithelial cells
Humans
Immune response
Immunotherapy
Lymphocytes T
Medical research
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Molecular modelling
Organs
Placenta
prophylaxis
Reproductive organs
Spleen
Stem cells
Surface markers
Tumor cells
Tumors
Vaccination
Vaccines
title Vaccination with human amniotic epithelial cells confer effective protection in a murine model of Colon adenocarcinoma
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T06%3A05%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Vaccination%20with%20human%20amniotic%20epithelial%20cells%20confer%20effective%20protection%20in%20a%20murine%20model%20of%20Colon%20adenocarcinoma&rft.jtitle=International%20journal%20of%20cancer&rft.au=Tabatabaei,%20M.&rft.date=2018-04-01&rft.volume=142&rft.issue=7&rft.spage=1453&rft.epage=1466&rft.pages=1453-1466&rft.issn=0020-7136&rft.eissn=1097-0215&rft_id=info:doi/10.1002/ijc.31159&rft_dat=%3Cproquest_cross%3E1999047124%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1999047124&rft_id=info:pmid/29139122&rfr_iscdi=true