Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 238
Gene Symbol: ALK
ALK
0.070 Biomarker phenotype BEFREE We subjected our ALK TKI-refractory cancer cells along with parental cancer cells to systematic miRNA expression arrays. 30791979 2019
Entrez Id: 238
Gene Symbol: ALK
ALK
0.070 GeneticVariation phenotype BEFREE While few of the mechanisms of clinical resistance to ALK inhibitors such as gene mutation are well known, there are others that are not well covered. 29143801 2017
Entrez Id: 238
Gene Symbol: ALK
ALK
0.070 GeneticVariation phenotype BEFREE Early data point to <i>ALK</i> G1202R and <i>ALK</i> E1210K as potential mechanisms of clinical resistance to brigatinib. 28435288 2017
Entrez Id: 238
Gene Symbol: ALK
ALK
0.070 Biomarker phenotype BEFREE Therefore, c-Met overexpression, HER-2 gene amplification, and SPTBN1-ALK gene fusion can coexist in lung adenocarcinoma and may become a potential biomarker of cancer refractory to crizotinib, chemotherapy, and radiotherapy as well as of a relatively poor prognosis. 27496196 2016
Entrez Id: 238
Gene Symbol: ALK
ALK
0.070 GeneticVariation phenotype BEFREE For example, the combination of ALK and MAPK kinase (MEK) inhibitors was active in an ALK-positive resistant tumor that had developed a MAP2K1 activating mutation, and the combination of EGFR and fibroblast growth factor receptor (FGFR) inhibitors was active in an EGFR mutant resistant cancer with a mutation in FGFR3. 25394791 2014
Entrez Id: 238
Gene Symbol: ALK
ALK
0.070 Biomarker phenotype BEFREE While excellent clinical response has been observed in many patients, the acquisition of clinical resistance to ALK inhibition highlights the need for development of second-generation ALK kinase inhibitors and/or combination therapies that target downstream signaling mediators or antibody drug conjugates. 23696342 2013
Entrez Id: 238
Gene Symbol: ALK
ALK
0.070 Biomarker phenotype BEFREE Our study identifies multiple novel mutations in ALK that may confer clinical resistance to crizotinib, suggests that crizotinib's narrow selectivity window may underlie its susceptibility to such resistance and demonstrates that a more potent ALK inhibitor may be effective at overcoming resistance. 22034911 2011