PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 33895784-0 2021 Combination efficacy of ruxolitinib with standard-of-care drugs in CRLF2-rearranged Ph-like acute lymphoblastic leukemia. ruxolitinib 24-35 cytokine receptor like factor 2 Homo sapiens 67-72 34591931-8 2021 Moreover, differences in sensitivity of two CRLF2-drivenBCP-ALL cell lines to ruxolitinib were also seen. ruxolitinib 78-89 cytokine receptor like factor 2 Homo sapiens 44-49 34505882-8 2021 In summary, IKZF1 deletion and a switch from cytokine dependence to activated BCR-like signaling phenotype represent putative mechanisms of ruxolitinib resistance in this case, recapitulating preclinical data on resistance to JAK inhibition in CRLF2-rearranged Philadelphia chromosome-like acute lymphoblastic leukemia. ruxolitinib 140-151 cytokine receptor like factor 2 Homo sapiens 244-249 33895784-7 2021 Based on these findings, we conducted preclinical in vivo drug testing and demonstrated that ruxolitinib enhanced the in vivo efficacy of an induction-type regimen consisting of vincristine, dexamethasone, and L-asparaginase in 2/3 CRLF2-rearranged Ph-like ALL xenografts. ruxolitinib 93-104 cytokine receptor like factor 2 Homo sapiens 232-237 33895784-8 2021 Overall, our findings support evaluating the addition of ruxolitinib to conventional induction regimens for the treatment of CRLF2-rearranged Ph-like ALL. ruxolitinib 57-68 cytokine receptor like factor 2 Homo sapiens 125-130 27449287-4 2016 Of note, CRLF2 over-expression was associated with poor prognosis in the high risk (HR) subgroup where CRLF2-high patients were more frequently allocated.Interestingly, although in T-ALL CRLF2 protein was localized mainly in the cytoplasm, in CRLF2-high blasts we found a trend towards a stronger TSLP-induced pSTAT5 response, sensitive to the JAK inhibitor Ruxolitinib.In conclusion, CRLF2 over-expression is a poor prognostic marker identifying a subset of HR T-ALL patients that could benefit from alternative therapy, potentially targeting the CRLF2 pathway. ruxolitinib 358-369 cytokine receptor like factor 2 Homo sapiens 9-14 27777238-7 2017 Combined gedatolisib and ruxolitinib treatment of CRLF2/JAK-mutant models more effectively inhibited ALL proliferation than either inhibitor alone (P < .001) and further enhanced survival. ruxolitinib 25-36 cytokine receptor like factor 2 Homo sapiens 50-55 25976292-1 2015 BACKGROUND: Ruxolitinib, an orally bioavailable JAK1/JAK2 inhibitor, may treat cancers with CRLF2 and/or JAK pathway mutations. ruxolitinib 12-23 cytokine receptor like factor 2 Homo sapiens 92-97