Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 2 de 2
Filtrer
Plus de filtres










Base de données
Gamme d'année
1.
Molecules ; 28(2)2023 Jan 11.
Article de Anglais | MEDLINE | ID: mdl-36677787

RÉSUMÉ

Global reaction route mapping (GRRM) analysis for compounds with the formula C4H5NO allowed for the detection of the corresponding "Guinness molecules" 000 and 001, as well as around 150 other stable minima of the same composition. The results suggest that compounds of similar functionality form a kind of "Stability Island" with their free energies of formation falling within s relatively limited range.

2.
Immunity ; 56(1): 143-161.e11, 2023 01 10.
Article de Anglais | MEDLINE | ID: mdl-36630913

RÉSUMÉ

Although T cells can exert potent anti-tumor immunity, a subset of T helper (Th) cells producing interleukin-22 (IL-22) in breast and lung tumors is linked to dismal patient outcome. Here, we examined the mechanisms whereby these T cells contribute to disease. In murine models of lung and breast cancer, constitutional and T cell-specific deletion of Il22 reduced metastases without affecting primary tumor growth. Deletion of the IL-22 receptor on cancer cells decreases metastasis to a degree similar to that seen in IL-22-deficient mice. IL-22 induced high expression of CD155, which bound to the activating receptor CD226 on NK cells. Excessive activation led to decreased amounts of CD226 and functionally impaired NK cells, which elevated the metastatic burden. IL-22 signaling was also associated with CD155 expression in human datasets and with poor patient outcomes. Taken together, our findings reveal an immunosuppressive circuit activated by T cell-derived IL-22 that promotes lung metastasis.


Sujet(s)
Interleukines , Tumeurs , Récepteurs viraux , Lymphocytes T auxiliaires , Animaux , Humains , Souris , Antigènes de différenciation des lymphocytes T/métabolisme , Interleukines/génétique , Interleukines/métabolisme , Cellules tueuses naturelles/métabolisme , Tumeurs/métabolisme , Liaison aux protéines , Lymphocytes T auxiliaires/métabolisme ,
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE