Evidence map›Paper›PMID 38255882›Full record

ReviewInternational journal of molecular sciences2024

Natural Product-Based Glycolysis Inhibitors as a Therapeutic Strategy for Epidermal Growth Factor Receptor-Tyrosine Kinase Inhibitor-Resistant Non-Small Cell Lung Cancer.

Wonyoung Park, Jung Ho Han, Shibo Wei, Eun-Sun Yang, Se-Yun Cheon, Sung-Jin Bae, Dongryeol Ryu, Hwan-Suck Chung, Ki-Tae Ha

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
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  11. Cytotoxicity and Multi-Enzyme Inhibition ofPlants (Basel, Switzerland) · 2024
    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

9 authors at 5 institutions in 1 country.

Wonyoung ParkDepartment of Korean Medical Science, School of Korean Medicine, Pusan National University, Yangsan 50612, Republic of Korea.
Jung Ho HanKorean Medicine Application Center, Korea Institute of Oriental Medicine, Daegu 41062, Republic of Korea.ORCID 0000-0001-8471-6513
Shibo WeiDepartment of Molecular Cell Biology, School of Medicine, Sungkyunkwan University, Suwon 16419, Republic of Korea.ORCID 0000-0001-9283-9804
Eun-Sun YangKorean Medical Research Center for Healthy Aging, Pusan National University, Yangsan 50612, Republic of Korea.
Se-Yun CheonKorean Medical Research Center for Healthy Aging, Pusan National University, Yangsan 50612, Republic of Korea.
Sung-Jin BaeDepartment of Molecular Biology and Immunology, Kosin University College of Medicine, Busan 49267, Republic of Korea.ORCID 0000-0001-8975-0876
Dongryeol RyuDepartment of Biomedical Science and Engineering, Gwangju Institute of Science and Technology, Gwangju 61005, Republic of Korea.ORCID 0000-0001-5905-6760
Hwan-Suck ChungKorean Medicine Application Center, Korea Institute of Oriental Medicine, Daegu 41062, Republic of Korea.ORCID 0000-0002-5901-0217
Ki-Tae HaDepartment of Korean Medical Science, School of Korean Medicine, Pusan National University, Yangsan 50612, Republic of Korea.ORCID 0000-0001-6283-0171
Pusan National University · KRKorea Institute of Oriental Medicine · KRGwangju Institute of Science and Technology · KRKosin University · KRSungkyunkwan University · KR

Funding

National Research Foundation of Korea NRF-2021R1A4A1025662National Research Foundation of Korea NRF-2022R1A2C2005130National Research Foundation of Korea RS-2023-00237776
6 · The paper itself

Abstract

Non-small cell lung cancer (NSCLC) is a leading cause of cancer-related deaths worldwide. Targeted therapy against the epidermal growth factor receptor (EGFR) is a promising treatment approach for NSCLC. However, resistance to EGFR tyrosine kinase inhibitors (TKIs) remains a major challenge in its clinical management. EGFR mutation elevates the expression of hypoxia-inducible factor-1 alpha to upregulate the production of glycolytic enzymes, increasing glycolysis and tumor resistance. The inhibition of glycolysis can be a potential strategy for overcoming EGFR-TKI resistance and enhancing the effectiveness of EGFR-TKIs. In this review, we specifically explored the effectiveness of pyruvate dehydrogenase kinase inhibitors and lactate dehydrogenase A inhibitors in combating EGFR-TKI resistance. The aim was to summarize the effects of these natural products in preclinical NSCLC models to provide a comprehensive understanding of the potential therapeutic effects. The study findings suggest that natural products can be promising inhibitors of glycolytic enzymes for the treatment of EGFR-TKI-resistant NSCLC. Further investigations through preclinical and clinical studies are required to validate the efficacy of natural product-based glycolytic inhibitors as innovative therapeutic modalities for NSCLC.

Indexed as

Biological ProductsCarcinoma, Non-Small-Cell LungLung NeoplasmsErbB ReceptorsGlycolysisHumansTyrosine Kinase InhibitorsBiological ProductsErbB ReceptorsTyrosine Kinase InhibitorsEGFR-TKIglycolysis inhibitorLDHAnatural productsNSCLCPDK

Identifiers

PMID38255882
PMCPMC10815680
OpenAlexW4390737009

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.