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10.1681/asn.2022070750 173 RanJ.AiY.NiJ.ZhangY.ChenJ.WangT.et al (2025)
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In contrast, other targeted inhibitors—including Erlotinib and Gefitinib (targeting wild-type EGFR), Afatinib and WZ4002 (targeting mutant EGFR), and Tinodasertib and Tomivosertib (targeting MNK2 for MAPK inhibition)—failed to recapitulate the same degree of cell death-inducing effects of Osimertinib in A172, LN229, U251, and U87 glioblastoma cells (Supplementary Fig
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