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Developing Oncolytic Viruses for the Treatment of Cervical Cancer
Cervical cancer represents one of the most important malignancies among women worldwide. Current therapeutic approaches for cervical cancer are reported not only to be inadequate for metastatic cervical cancer, but are also considered as cytotoxic for several patients leading to serious side effects...
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Published in: | Cells (Basel, Switzerland) Switzerland), 2023-07, Vol.12 (14), p.1838 |
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description | Cervical cancer represents one of the most important malignancies among women worldwide. Current therapeutic approaches for cervical cancer are reported not only to be inadequate for metastatic cervical cancer, but are also considered as cytotoxic for several patients leading to serious side effects, which can have negative implications on the quality of life of women. Therefore, there is an urgent need for the development of innovative and effective treatment options. Oncolytic viruses can eventually become effective biological agents, since they preferentially infect and kill cancer cells, while leaving the normal tissue unaffected. Moreover, they are also able to leverage the host immune system response to limit tumor growth. This review aims to systematically describe and discuss the different types of oncolytic viruses generated for targeting cervical cancer cells, as well as the outcome of the combination of virotherapy with conventional therapies. Although many preclinical studies have evaluated the therapeutic efficacy of oncolytic viruses in cervical cancer, the number of clinical trials so far is limited, while their oncolytic properties are currently being tested in clinical trials for the treatment of other malignancies. |
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Current therapeutic approaches for cervical cancer are reported not only to be inadequate for metastatic cervical cancer, but are also considered as cytotoxic for several patients leading to serious side effects, which can have negative implications on the quality of life of women. Therefore, there is an urgent need for the development of innovative and effective treatment options. Oncolytic viruses can eventually become effective biological agents, since they preferentially infect and kill cancer cells, while leaving the normal tissue unaffected. Moreover, they are also able to leverage the host immune system response to limit tumor growth. This review aims to systematically describe and discuss the different types of oncolytic viruses generated for targeting cervical cancer cells, as well as the outcome of the combination of virotherapy with conventional therapies. Although many preclinical studies have evaluated the therapeutic efficacy of oncolytic viruses in cervical cancer, the number of clinical trials so far is limited, while their oncolytic properties are currently being tested in clinical trials for the treatment of other malignancies.</description><identifier>ISSN: 2073-4409</identifier><identifier>EISSN: 2073-4409</identifier><identifier>DOI: 10.3390/cells12141838</identifier><identifier>PMID: 37508503</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adenoviruses ; Angiogenesis ; cancer immunotherapy ; Cancer therapies ; Care and treatment ; Cell cycle ; Cell growth ; Cervical cancer ; Clinical trials ; Cytotoxicity ; FDA approval ; Human papillomavirus ; Immune system ; Immunotherapy ; innate immunity ; Malignancy ; Medical prognosis ; Medical screening ; Metastases ; Metastasis ; Oncolysis ; oncolytic viruses ; Prevention ; Proteins ; Quality of life ; Review ; Tumors ; viral vectors ; virotherapy ; Viruses</subject><ispartof>Cells (Basel, Switzerland), 2023-07, Vol.12 (14), p.1838</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 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/). 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Current therapeutic approaches for cervical cancer are reported not only to be inadequate for metastatic cervical cancer, but are also considered as cytotoxic for several patients leading to serious side effects, which can have negative implications on the quality of life of women. Therefore, there is an urgent need for the development of innovative and effective treatment options. Oncolytic viruses can eventually become effective biological agents, since they preferentially infect and kill cancer cells, while leaving the normal tissue unaffected. Moreover, they are also able to leverage the host immune system response to limit tumor growth. This review aims to systematically describe and discuss the different types of oncolytic viruses generated for targeting cervical cancer cells, as well as the outcome of the combination of virotherapy with conventional therapies. Although many preclinical studies have evaluated the therapeutic efficacy of oncolytic viruses in cervical cancer, the number of clinical trials so far is limited, while their oncolytic properties are currently being tested in clinical trials for the treatment of other malignancies.</description><subject>Adenoviruses</subject><subject>Angiogenesis</subject><subject>cancer immunotherapy</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Cell cycle</subject><subject>Cell growth</subject><subject>Cervical cancer</subject><subject>Clinical trials</subject><subject>Cytotoxicity</subject><subject>FDA approval</subject><subject>Human papillomavirus</subject><subject>Immune system</subject><subject>Immunotherapy</subject><subject>innate immunity</subject><subject>Malignancy</subject><subject>Medical prognosis</subject><subject>Medical screening</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Oncolysis</subject><subject>oncolytic viruses</subject><subject>Prevention</subject><subject>Proteins</subject><subject>Quality of life</subject><subject>Review</subject><subject>Tumors</subject><subject>viral vectors</subject><subject>virotherapy</subject><subject>Viruses</subject><issn>2073-4409</issn><issn>2073-4409</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1v1DAQhiMEolXpkSuKxIVLip3xV05otYW2UqVeClfLccZbr5J4sZOV-u9x2FK6iPHB1viZdzzjKYr3lFwANOSzxb5PtKaMKlCvitOaSKgYI83rF-eT4jylLcmmqKCEvy1OQHKiOIHTYnWJe-zDzo-b8m60oX-cvC1_-DgnTKULsZwesLyPaKYBx6kMrlxj3Htr-nJtRovxXfHGmT7h-dN-Vnz_9vV-fV3d3l3drFe3leWsmSorpWCSSlCdqVktrKW86zrVokRGRS2o4IqioxItqSlxAiwFzq2TBhRyOCtuDrpdMFu9i34w8VEH4_VvR4gbbWJ-fI8aWsagoRRtzsnatmm4U4DOkFZIIVXW-nLQ2s3tgJ3NlUXTH4ke34z-QW_CXlMCMpvICp-eFGL4OWOa9ODT8h1mxDAnXaul9UoAy-jHf9BtmOOYe7VQQECxuvlLbUyuwI8u5MR2EdUryVVDeQMLdfEfKq8OB2_DiM5n_1FAdQiwMaQU0T0XSYleZkgfzVDmP7zszDP9Z2LgF5zLvxI</recordid><startdate>20230701</startdate><enddate>20230701</enddate><creator>Kalafati, Eleni</creator><creator>Drakopoulou, Ekati</creator><creator>Anagnou, Nicholas P</creator><creator>Pappa, Kalliopi I</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-7130-5192</orcidid><orcidid>https://orcid.org/0000-0001-6246-3885</orcidid></search><sort><creationdate>20230701</creationdate><title>Developing Oncolytic Viruses for the Treatment of Cervical Cancer</title><author>Kalafati, Eleni ; Drakopoulou, Ekati ; Anagnou, Nicholas P ; Pappa, Kalliopi I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c549t-c776471738da2426cc15ddd8be7e4162616581ef17ec0210f63c1355cf7a38e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adenoviruses</topic><topic>Angiogenesis</topic><topic>cancer immunotherapy</topic><topic>Cancer therapies</topic><topic>Care and treatment</topic><topic>Cell cycle</topic><topic>Cell growth</topic><topic>Cervical cancer</topic><topic>Clinical trials</topic><topic>Cytotoxicity</topic><topic>FDA approval</topic><topic>Human papillomavirus</topic><topic>Immune system</topic><topic>Immunotherapy</topic><topic>innate immunity</topic><topic>Malignancy</topic><topic>Medical prognosis</topic><topic>Medical screening</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Oncolysis</topic><topic>oncolytic viruses</topic><topic>Prevention</topic><topic>Proteins</topic><topic>Quality of life</topic><topic>Review</topic><topic>Tumors</topic><topic>viral vectors</topic><topic>virotherapy</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kalafati, Eleni</creatorcontrib><creatorcontrib>Drakopoulou, Ekati</creatorcontrib><creatorcontrib>Anagnou, Nicholas P</creatorcontrib><creatorcontrib>Pappa, Kalliopi I</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest - 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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJÂ Directory of Open Access Journals</collection><jtitle>Cells (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kalafati, Eleni</au><au>Drakopoulou, Ekati</au><au>Anagnou, Nicholas P</au><au>Pappa, Kalliopi I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Developing Oncolytic Viruses for the Treatment of Cervical Cancer</atitle><jtitle>Cells (Basel, Switzerland)</jtitle><addtitle>Cells</addtitle><date>2023-07-01</date><risdate>2023</risdate><volume>12</volume><issue>14</issue><spage>1838</spage><pages>1838-</pages><issn>2073-4409</issn><eissn>2073-4409</eissn><abstract>Cervical cancer represents one of the most important malignancies among women worldwide. 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subjects | Adenoviruses Angiogenesis cancer immunotherapy Cancer therapies Care and treatment Cell cycle Cell growth Cervical cancer Clinical trials Cytotoxicity FDA approval Human papillomavirus Immune system Immunotherapy innate immunity Malignancy Medical prognosis Medical screening Metastases Metastasis Oncolysis oncolytic viruses Prevention Proteins Quality of life Review Tumors viral vectors virotherapy Viruses |
title | Developing Oncolytic Viruses for the Treatment of Cervical Cancer |
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