Evidence mapPaperPMID 41359225Full record

ReviewArchives of pharmacal research2026

Harnessing transcriptomics for discovery of natural products to overcome acquired cancer resistance.

Heerim Yeo, Sang-Yun Kim, Sang-Min Park

Abstract readReview
PubMed Publisher
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

3 authors.

Heerim Yeo *College of Pharmacy, Chungnam National University, Daejeon, 34134, Republic of Korea.
Sang-Yun Kim *College of Pharmacy, Chungnam National University, Daejeon, 34134, Republic of Korea.
Sang-Min ParkCollege of Pharmacy, Chungnam National University, Daejeon, 34134, Republic of Korea. smpark@cnu.ac.kr.ORCID http://orcid.org/0000-0003-2915-0742

Funding

Korea Institute of Oriental Medicine KSN1722122National Research Foundation of Korea RS-2023-00210923National Research Foundation of Korea RS-2025-25397599
6 · The paper itself

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

Antineoplastic AgentsBiological ProductsDrug DiscoveryDrug Resistance, NeoplasmNeoplasmsTranscriptomeAnimalsGene Expression ProfilingHumansAntineoplastic AgentsBiological ProductsAcquired resistanceBioinformaticsDrug repurposingSystems pharmacologyTargeted therapyTranscriptomics

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.