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10.18632/oncotarget.19929

http://scihub22266oqcxt.onion/10.18632/oncotarget.19929
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suck abstract from ncbi


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pmid28969098      Oncotarget 2017 ; 8 (38): 64607-21
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  • CAR-T cell therapy in ovarian cancer: from the bench to the bedside #MMPMID28969098
  • Zhu X; Cai H; Zhao L; Ning L; Lang J
  • Oncotarget 2017[Sep]; 8 (38): 64607-21 PMID28969098show ga
  • Ovarian cancer (OC) is the most lethal gynecological malignancy and is responsible for most gynecological cancer deaths. Apart from conventional surgery, chemotherapy, and radiotherapy, chimeric antigen receptor-modified T (CAR-T) cells as a representative of adoptive cellular immunotherapy have received considerable attention in the research field of cancer treatment. CARs combine antigen specificity and T-cell-activating properties in a single fusion molecule. Several preclinical experiments and clinical trials have confirmed that adoptive cell immunotherapy using typical CAR-engineered T cells for OC is a promising treatment approach with striking clinical efficacy; moreover, the emerging CAR-Ts targeting various antigens also exert great potential. However, such therapies have side effects and toxicities, such as cytokine-associated and ?on-target, off-tumor? toxicities. In this review, we systematically detail and highlight the present knowledge of CAR-Ts including the constructions, vectors, clinical applications, development challenges, and solutions of CAR-T-cell therapy for OC. We hope to provide new insight into OC treatment for the future.
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