| Literature DB >> 33745426 |
Monireh Mohsenzadegan1, Parizad Bavandpour2, Mohammad Reza Nowroozi3, Erfan Amini3, Masoumeh Kourosh-Arami4, Seyed Ali Momeni5, Saied Bokaie6, Laleh Sharifi3.
Abstract
Targeting inhibitory receptors on T cells in the tumor sites can promote effective anti-tumor immunity in bladder cancer. Unfortunately, the main dilemma is that a large number of patients remain refractory to CTLA-4, PD-1, and PD-L1 blockade therapies. T-cell immunoglobulin and mucin domain 3 (Tim-3) is an inhibitory receptor expressed on T cells and innate immune cells. Both in vivo and in vitro data from patients with advanced cancers support the role of Tim-3 inhibition in satisfactory anti-tumor immunity. In bladder cancer, the expression level of Tim-3 significantly increases with advanced pathological grade and T stage. Therefore, rationality implies that designing novel monoclonal antibodies reactive with Tim-3 alone or in combination with other checkpoint inhibitors may indicate a favorable response in bladder cancer. Here, we aimed to investigate the possibility of targeting Tim-3 as a novel anti-cancer treatment for bladder cancer. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.Entities:
Keywords: Bladder cancer; T-cell immunoglobulin and mucin domain 3 (TIM-3); anti-cancer treatment.; checkpoint inhibitor; immunotherapy; inhibitory receptor; monoclonal antibodies
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Year: 2021 PMID: 33745426 DOI: 10.2174/1871530321666210310142141
Source DB: PubMed Journal: Endocr Metab Immune Disord Drug Targets ISSN: 1871-5303 Impact factor: 2.895