ReviewArchives of pharmacal research2026
Harnessing transcriptomics for discovery of natural products to overcome acquired cancer resistance.
Review in Archives of pharmacal research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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
2 citing papers in PubMed.
- Wogonin Ameliorates the Oxidative Stress, Apoptosis, and Extracellular Matrix Degradation of Nucleus Pulposus Cells Mediated byInternational journal of molecular sciences · 2026Article
- Palmaturbine Inhibits Pancreatic Ductal Adenocarcinoma by Suppressing the JAK2/STAT3 Signaling Pathway.International journal of molecular sciences · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
Targeted cancer therapy is often compromised by the development of acquired drug resistance. Beyond genetic mutations, recent studies underscore the role of non-genetic plasticity and adaptive network rewiring in driving this resistance. Overcoming this challenge requires innovative approaches, including the integration of transcriptomics and natural product research. Natural products are chemically diverse agents that can modulate multiple resistance pathways due to their polypharmacological properties. In parallel, transcriptomic profiling of drug-exposed cells provides genome-wide snapshots of resistance states and reveals how candidate compounds remodel these cells. This review summarizes the methods by which transcriptomics facilitates the identification of natural products that overcome resistance to targeted therapies. It outlines the canonical resistance mechanisms and highlights the natural products that reverse these adaptive networks at the molecular level. It then discusses how systematic transcriptomic workflows, including differential expression profiling, pathway analysis, and perturbome matching, elucidate the modes of action of natural compounds. This data-driven framework facilitates the discovery of novel agents, supports drug repurposing, and guides the rational design of combination therapies to restore drug sensitivity. Finally, it addresses clinical translation barriers and emerging computational frontiers, such as multi-omics and artificial intelligence, which will increasingly play vital roles in harnessing the therapeutic potential of natural products in patients with resistant cancers.
Indexed as
Identifiers
41359225What Socratic 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 Socratic graph.