<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(4)</volume><submitter>Zhang X</submitter><pubmed_abstract>Insufficient infiltration or dysfunction of lymphocytes in the tumor immune microenvironment is considered to be a contributing factor to poor immunotherapy outcomes in solid tumors. Necroptosis, a form of immunogenic cell death, has attracted increasing interest because of its unique role in regulating tumor immune responses. CL-387785, a third-generation EGFR inhibitor, has been reported to inhibit tumors by regulating the cell cycle and inducing apoptosis; however, the underlying mechanisms remain unclear. In this study, we demonstrated that CL-387785 effectively suppressed the malignant phenotype of melanoma and lung cancer and confirmed that cancer cells undergo necroptosis, as evidenced by morphological and protein-level analyses. Further in vivo and in vitro experiments revealed tha</pubmed_abstract><journal>International journal of biological sciences</journal><pagination>2085-2100</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12905644</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Targeted Induction of Cancer Cell Necroptosis Potentiates Anti-PD-1 Immunotherapy via CD80 Activation.</pubmed_title><pmcid>PMC12905644</pmcid><pubmed_authors>Zhang D</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Peng C</pubmed_authors><pubmed_authors>Xiong S</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Zhou Z</pubmed_authors><pubmed_authors>Liu W</pubmed_authors><pubmed_authors>Zhu S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Targeted Induction of Cancer Cell Necroptosis Potentiates Anti-PD-1 Immunotherapy via CD80 Activation.</name><description>Insufficient infiltration or dysfunction of lymphocytes in the tumor immune microenvironment is considered to be a contributing factor to poor immunotherapy outcomes in solid tumors. Necroptosis, a form of immunogenic cell death, has attracted increasing interest because of its unique role in regulating tumor immune responses. CL-387785, a third-generation EGFR inhibitor, has been reported to inhibit tumors by regulating the cell cycle and inducing apoptosis; however, the underlying mechanisms remain unclear. In this study, we demonstrated that CL-387785 effectively suppressed the malignant phenotype of melanoma and lung cancer and confirmed that cancer cells undergo necroptosis, as evidenced by morphological and protein-level analyses. Further in vivo and in vitro experiments revealed tha</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026</publication><modification>2026-07-15T22:19:08.729Z</modification><creation>2026-07-09T10:20:30.463Z</creation></dates><accession>S-EPMC12905644</accession><cross_references><pubmed>41694588</pubmed><doi>10.7150/ijbs.121690</doi></cross_references></HashMap>