<HashMap><database>iProX</database><scores/><additional><omics_type>Proteomics</omics_type><submitter>Limin Wang</submitter><species>Homo Sapiens</species><full_dataset_link>http://www.iprox.org/page/project.html?id=IPX0017774000</full_dataset_link><submitter_email>wanglimin@hebeu.edu.cn</submitter_email><submitter_affiliation>Hebei University of Engineering</submitter_affiliation><sample_protocol></sample_protocol><repository>iProX</repository><data_protocol></data_protocol><pubmed_abstract>Non-small cell lung cancer (NSCLC) remains a leading cause of cancer-related mortality worldwide, with limited therapeutic efficacy and severe side effects associated with conventional chemotherapy, creating an urgent need for safe and effective natural anti-tumor agents. Quercetagetin-rich marigold flavonoids (QG-MF), isolated from the lutein-extracted inflorescence residues of &lt;i>Tagetes erecta&lt;/i> L. (marigold), have been identified as bioactive polyphenols with potential anti-cancer properties, yet their anti-NSCLC activity and underlying molecular mechanisms remain elusive.&lt;h4>Aim of the study&lt;/h4>This study aimed to investigate the &lt;i>in vitro&lt;/i> and &lt;i>in vivo&lt;/i> inhibitory effects of QG-MF on NSCLC.&lt;h4>Methods&lt;/h4>&lt;i>In vitro&lt;/i> experiments were performed on A549 and H661 NSCLC cell lines: cell proliferation was detected by CCK-8 assay; cell migration and invasion were evaluated via wound healing and Transwell assays, respectively; cell apoptosis and cycle distribution were analyzed by flow cytometry; the expression levels of p53/p21 signaling pathway-related proteins were determined by Western blot. &lt;i>In vivo&lt;/i> anti-tumor efficacy of QG-MF was assessed using A549 NSCLC xenograft mouse models, with tumor volume and weight measured to evaluate tumor growth inhibition.&lt;h4>Results&lt;/h4>QG-MF significantly suppressed proliferation, migration and invasion, and induced apoptosis as well as cell cycle arrest in A549 and H661 cells in a concentration-dependent manner. Mechanistically, QG-MF upregulated the expression of p53, p21, Bax and caspase-3, and downregulated Bcl-2 in NSCLC cells. Furthermore, siRNA-mediated p53 silencing effectively abrogated the anti-proliferative and pro-apoptotic effects of QG-MF on NSCLC cells. &lt;i>In vivo&lt;/i>, QG-MF markedly inhibited the growth of A549 xenograft tumors in nude mice without obvious systemic toxicity.&lt;h4>Conclusion&lt;/h4>Our findings demonstrate that QG-MF exerts potent anti-NSCLC activity by inducing apoptosis and inhibiting proliferation/metastasis via the p53/p21 signaling pathway.</pubmed_abstract><pubmed_title>Quercetagetin-rich flavonoids from marigold induce apoptosis inhibit metastasis of non-small cell lung cancer via the p53/p21 signaling pathway.</pubmed_title><pubmed_authors>Dong Zhihuan Z, Cheng Xinying X, Lian Yunhe Y, Wu Di D, Liu Kaihui K, Feng Xue X, Xue Qiang Q, Chen Qingliang Q, Wang Limin L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Quercetagetin-rich flavonoids (QG-MF) from marigold induce apoptosis via activating p53/p21 pathway in non-small cell lung cancer cells</name><description>Label-free quantitative proteomics was applied to screen differentially expressed proteins in QG-MF-treated A549 lung cancer cells. Functional enrichment analysis and in vitro/in vivo validation confirmed the regulation of the p53/p21 signaling cascade. All mass spectrometry raw data and processed analytical files are deposited in compliance with MIAPE guidelines for ProteomeXchange.</description><dates><publication>Mon Jun 15 00:00:00 GMT+01:00 2026</publication></dates><accession>PXD079740</accession><cross_references><TAXONOMY>9606</TAXONOMY><pubmed>42434755</pubmed></cross_references></HashMap>