ReviewDrug design, development and therapy2026
Anti-Lung Cancer Agent Discovery and Development: A Review of Cross-Platform Correlation Across in silico, Network Pharmacology, in vitro, and in vivo Assessments.
Review in Drug design, development and therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Lung cancer remains one of the leading causes of cancer-related mortality worldwide, highlighting the urgent need for more effective and clinically translatable therapeutic agents. In recent years, drug discovery strategies integrating computational modeling with experimental validation have gained increasing attention; however, their predictive consistency across biological scales remains a critical challenge. This review systematically synthesises evidence from eleven primary studies that evaluated anti-lung cancer agents across computational, cellular, and organism-level platforms within a single developmental continuum. Eligible studies were required to report either in silico target prediction/molecular docking or network pharmacology analysis (or both), in direct conjunction with in vitro cytotoxic evaluation and in vivo efficacy assessment. Relevant studies were identified using a structured Boolean keyword strategy integrating computational, cellular, animal-based, and lung cancer-specific terms. Across the analyzed studies, computational and network approaches consistently converged on key oncogenic signaling hubs, particularly PI3K/AKT-centered pathways and receptor tyrosine kinases. These predictions were corroborated by cellular assays demonstrating selective antiproliferative activity in lung cancer cell lines and subsequently validated in animal models showing significant tumor growth suppression with acceptable safety profiles. Notably, agents optimized through targeted delivery systems, formulation strategies, or rational combination therapies exhibited the most consistent cross-platform performance. Collectively, the findings highlight that robust anti-lung cancer efficacy is most reliably achieved when molecular interaction data, systems-level network engagement, cellular responses, and in vivo outcomes are coherently integrated. This integrated evaluation framework provides a rational and predictive foundation for future anti-lung cancer drug discovery and development.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.