Evidence map›Paper›PMID 42718449›Full record

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.

Sandra Megantara, Rohani Rohani, M Rahmatullah Zakaria, M Theodorik S Biu, Ezatul Ezleen Kamarulzaman, Agus Rusdin

Abstract readReview
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Sandra MegantaraDepartment of Analytical Pharmacy and Medicinal Chemistry, Faculty of Pharmacy, Universitas Padjadjaran (UNPAD), Bandung, Indonesia.ORCID 0000-0003-4951-7740
Rohani RohaniDepartment of Pharmacology and Clinical Pharmacy, Faculty of Pharmacy, Universitas Padjadjaran (UNPAD), Bandung, Indonesia.ORCID 0009-0004-9366-5235
M Rahmatullah ZakariaTechnology Development Division, Research & Development Pharma, PT. Kalbe Farma, Bekasi, Indonesia.
M Theodorik S BiuPolice Medical and Health Center (Pusdokkes), Indonesian National Police, Jakarta, Indonesia.
Ezatul Ezleen KamarulzamanDepartment of Pharmaceutical Chemistry, School of Pharmaceutical Sciences, Universiti Sains Malaysia, Pulau Pinang, Malaysia.ORCID 0000-0003-0635-1023
Agus RusdinDepartment of Pharmacy, Jakarta Global University, Depok, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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

Antineoplastic AgentsComputer SimulationDrug DevelopmentDrug DiscoveryLung NeoplasmsNetwork PharmacologyAnimalsCell ProliferationHumansSignal TransductionAntineoplastic Agentsanticancercancerclinical trialin silicoin vitroin vivo

Identifiers

PMID42718449
PMCPMC13553333

What OpenQuestion holds

Textmetadata
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Registered trials

None linked

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.