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dc.contributor.authorTaghizadeh-Hesary, Farzad
dc.contributor.authorGhadyani, Mobina
dc.contributor.authorKashanchi, Fatah
dc.contributor.authorBehnam, Babak
dc.date.accessioned2024-09-06T15:10:07Z
dc.date.available2024-09-06T15:10:07Z
dc.date.issued2024-08-31
dc.identifierhttps://chesterrep.openrepository.com/bitstream/handle/10034/628986/cancers-16-03044.pdf?sequence=2
dc.identifier.citationTaghizadeh-Hesary, F., Ghadyani, M., Kashanchi, F., & Behnam, B. (2024). Exploring TSGA10 function: A crosstalk or controlling mechanism in the signaling pathway of carcinogenesis? Cancers, 16(17), article-number 3044. https://doi.org/10.3390/cancers16173044en_US
dc.identifier.doi10.3390/cancers16173044en_US
dc.identifier.urihttp://hdl.handle.net/10034/628986
dc.description.abstractCancer-specific antigens have been a significant area of focus in cancer treatment since their discovery in the mid-twentieth century. Cancer germline antigens are a class of antigens specifically overexpressed in germline tissues and cancer cells. Among these, TSGA10 (testis-specific gene antigen 10) is of great interest because of its crucial impact on cancer progression. Early studies explored TSGA10 expression in a variety of cancer types. More recent studies revealed that TSGA10 can suppress tumor progression by blocking cancer cell metabolism, angiogenesis, and metastasis. An open question regarding the TSGA10 is why cancer cells must express a protein that prevents their progression. To answer this question, we conducted a comprehensive review to engage the TSGA10 in the context of the current understanding of “malignant transformation”. This review demonstrated that TSGA10 expression level in cancer cells depends on the cancer stage across malignant transformation. In addition, we evaluated how TSGA10 expression can prevent the “cancer hallmarks”. Given this information, TSGA10 can be of great interest in developing effective targeted anti-cancer therapies.en_US
dc.description.sponsorshipUnfundeden_US
dc.languageen
dc.publisherMDPIen_US
dc.relation.urlhttps://www.mdpi.com/2072-6694/16/17/3044en_US
dc.rightsLicence for VoR version of this article: https://creativecommons.org/licenses/by/4.0/
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.subjectCanceren_US
dc.subjectTumor microenvironmenten_US
dc.subjectTSGA10en_US
dc.subjectTumor suppressoren_US
dc.subjectCancer germline antigenen_US
dc.titleExploring TSGA10 function: A crosstalk or controlling mechanism in the signaling pathway of carcinogenesis?en_US
dc.typeArticleen_US
dc.identifier.eissn2072-6694en_US
dc.contributor.departmentIran University of Medical Sciences; University of Chester; George Mason University; Avicenna Biotech Researchen_US
dc.identifier.journalCancersen_US
dc.date.updated2024-09-06T12:48:37Z
dc.date.accepted2024-08-28
rioxxterms.identifier.projectUnfundeden_US
rioxxterms.versionVoRen_US
dc.date.deposited2024-09-06en_US


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