Targeting cancer cells: from historic methods to modern chimeric antigen receptor (CAR) T-Cell strategies

dc.contributor.authorSaleh, Kochar Khasro
dc.contributor.authorDalkilic, Semih
dc.contributor.authorDalkilic, Lutfiye Kadioglu
dc.contributor.authorHamarashid, Bahra Radhaa
dc.contributor.authorKirbag, Sevda
dc.date.accessioned2026-08-12T17:08:30Z
dc.date.issued2020
dc.departmentFırat Üniversitesi
dc.description.abstractCancer therapy and diagnosis have long been challenges for humans. Despite accumulated knowledge and information, there are many complications and difficulties with cancer therapy and diagnosis. The challenges of cancer treatment are modified according to the new forms that have been discovered by researchers. Each stage of development has involved new techniques for cancer therapy, culminating in the modern immunotherapy approach using chimeric antigen receptor (CAR) cytotoxic T lymphocytes. This strategy is an example of the latest version of cancer cell therapy. Chimeric antigen receptor T-cell therapy drew interest soon after its implementation by researchers as a new strategy to control various types of cancer cells, and it is considered a living drug in the body that detects and destroys cancer cells in a long-term manner, with CAR T-cells remaining as memory cells. CAR T-cell therapy has shown remarkable effects against both primary acute lymphoblastic leukemia (ALL) and relapsed ALL, with a high remission rate observed in adults and children (approximately 90%). Although the use of CAR T-cell therapy for solid tumors has encountered obstacles associated with the microenvironment and immunosuppression, researchers are poised to improve effective CAR T-cell therapy for solid tumors. In this mini review, we describe some attempts that have applied CAR T-cells from the past and present; in addition, it contains many aspects of new anticancer strategies featuring CAR T-cells, especially CAR T-cell killing mechanisms.
dc.identifier.doi10.3934/Allergy.2020004
dc.identifier.endpage49
dc.identifier.issn2575-615X
dc.identifier.issue2
dc.identifier.orcid0000-0002-4337-8236
dc.identifier.orcid0000-0002-6892-247X
dc.identifier.startpage32
dc.identifier.urihttps://doi.org/10.3934/Allergy.2020004
dc.identifier.urihttps://hdl.handle.net/11508/50101
dc.identifier.volume4
dc.identifier.wosWOS:000544812600002
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherAmer Inst Mathematical Sciences-Aims
dc.relation.ispartofAims Allergy and Immunology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WoS_20260511
dc.subjectcancer
dc.subjectimmunotherapy
dc.subjectchimeric antigen receptor T-cell
dc.titleTargeting cancer cells: from historic methods to modern chimeric antigen receptor (CAR) T-Cell strategies
dc.typeReview Article

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