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1.
Frontiers of Medicine ; (4): 805-822, 2023.
Article Dans Anglais | WPRIM | ID: wpr-1010820

Résumé

Immunotherapies based on immune checkpoint blockade (ICB) have significantly improved patient outcomes and offered new approaches to cancer therapy over the past decade. To date, immune checkpoint inhibitors (ICIs) of CTLA-4 and PD-1/PD-L1 represent the main class of immunotherapy. Blockade of CTLA-4 and PD-1/PD-L1 has shown remarkable efficacy in several specific types of cancers, however, a large subset of refractory patients presents poor responsiveness to ICB therapy; and the underlying mechanism remains elusive. Recently, numerous studies have revealed that metabolic reprogramming of tumor cells restrains immune responses by remodeling the tumor microenvironment (TME) with various products of metabolism, and combination therapies involving metabolic inhibitors and ICIs provide new approaches to cancer therapy. Nevertheless, a systematic summary is lacking regarding the manner by which different targetable metabolic pathways regulate immune checkpoints to overcome ICI resistance. Here, we demonstrate the generalized mechanism of targeting cancer metabolism at three crucial immune checkpoints (CTLA-4, PD-1, and PD-L1) to influence ICB therapy and propose potential combined immunotherapeutic strategies co-targeting tumor metabolic pathways and immune checkpoints.


Sujets)
Humains , Anticorps monoclonaux/pharmacologie , Antigène CD274/antagonistes et inhibiteurs , Antigène CTLA-4/antagonistes et inhibiteurs , Inhibiteurs de points de contrôle immunitaires/pharmacologie , Tumeurs/traitement médicamenteux , Récepteur-1 de mort cellulaire programmée , Microenvironnement tumoral
2.
Chinese Journal of Physical Medicine and Rehabilitation ; (12)2003.
Article Dans Chinois | WPRIM | ID: wpr-682085

Résumé

0.05). (2) The average squeezing anal pressure and the duration of anal squeezing decreased in the experiment group, which were significantly different from those in the control group ( P

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