mProX™ Human ALK Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 ALK inhibitors inhibit or partially inhibit the proliferation of neuroblastoma cell lines harboring ALK aberrations.
Dose response curves of neuroblastoma cell lines with ALK mutations or increased expression subjected to ceritinib, crizotinib, alectinib, and PF06463922, four ALK inhibitors.
Ref: Wang, Hui Qin, et al. "Combined ALK and MDM2 inhibition increases antitumor activity and overcomes resistance in human ALK mutant neuroblastoma cell lines and xenograft models." Elife 6 (2017): e17137.
Pubmed: 28425916
DOI: 10.7554/eLife.17137
Research Highlights
When treating ALK-positive non-small-cell lung cancer (NSCLC), alexib, a highly selective inhibitor of anaplastic lymphoma kinase (ALK), has demonstrated systemic and central nervous system (CNS) efficacy.
Peters, Solange, et al. "Alectinib versus crizotinib in untreated ALK-positive non-small-cell lung cancer." New England Journal of Medicine 377.9 (2017): 829-838.
Pubmed:
28586279
DOI:
10.1056/NEJMoa1704795
When crizotinib was no longer effective for treating patients with ALK-positive NSCLC, alexitab demonstrated clinical activity and was well tolerated. Therefore, individuals with ALK-positive illness who have not responded well to crizotinib may benefit from alectinib therapy.
Shaw, Alice T., et al. "Alectinib in ALK-positive, crizotinib-resistant, non-small-cell lung cancer: a single-group, multicentre, phase 2 trial." The lancet oncology 17.2 (2016): 234-242.
Pubmed:
26708155
DOI:
10.1016/S1470-2045(15)00488-X