ArticleInternational journal of molecular sciences2026
From Mechanisms to Therapeutic Innovation in Non-Small Cell Lung Cancer: A Knowledge-Depth Translational Mapping with Experimental Validation.
Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Abstract
backgroundNon-small-cell lung cancer (NSCLC) research has transitioned from tumor-intrinsic mechanisms to immune-driven therapeutic innovation; however, the translation of mechanistic insights into clinically actionable strategies remains incompletely defined.
methodsA total of 1213 records were retrieved from the Web of Science Core Collection (SCI-Expanded) (2009-2025). After data cleaning and duplicate removal (n = 13), 1200 publications were analyzed. Bibliometrix (R) and CiteSpace were used for performance analysis, keyword mapping, thematic evolution, and co-citation clustering.
resultsAnnual scientific production increased markedly after 2018, paralleling the expansion of immunotherapy. Keyword co-occurrence identified three major thematic domains (>40 high-frequency keywords) linking molecular mechanisms, biomarkers, and therapeutic strategies. Thematic mapping highlighted immunotherapy, tumor microenvironment, and PD-1 as dominant motor themes, while resistance-related pathways formed a central mechanistic-translational axis. Thematic evolution demonstrated a shift from EGFR-targeted therapy to epithelial-mesenchymal transition (EMT)-centered resistance and subsequently to immune-dominant strategies. Co-citation clustering produced robust structures (Q ≈ 0.62; silhouette ≈ 0.84), identifying EMT as a persistent mechanistic hub. Pilot ELISA validation confirmed significant increases in TGF-β1 (~2.05-fold), IL-6 (~2.59-fold), CCL2 (~2.10-fold), and PD-L1 (~2.56-fold) under EMT-inducing conditions (
conclusionsThis integrative approach provides a quantitative and experimentally supported framework linking mechanistic insights to therapeutic innovation in NSCLC.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.