Evidence map›Paper›PMID 38792080›Full record

ArticleMolecules (Basel, Switzerland)2024

3-Hydroxytanshinone Inhibits the Activity of Hypoxia-Inducible Factor 1-α by Interfering with the Function of α-Enolase in the Glycolytic Pathway.

Tae Hyun Son, Shin-Hye Kim, Hye-Lim Shin, Dongsoo Kim, Hwan Gyu Kim, Yongseok Choi, Sik-Won Choi

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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

7 authors.

Tae Hyun SonSchool of Life Sciences and Biotechnology, Korea University, Seoul 02841, Republic of Korea.
Shin-Hye KimForest Biomaterials Research Center, National Institute of Forest Science (NIFoS), Jinju 52817, Republic of Korea.ORCID 0000-0002-8886-1133
Hye-Lim ShinForest Biomaterials Research Center, National Institute of Forest Science (NIFoS), Jinju 52817, Republic of Korea.
Dongsoo KimForest Biomaterials Research Center, National Institute of Forest Science (NIFoS), Jinju 52817, Republic of Korea.
Hwan Gyu KimDepartment of Biological Sciences, Jeonbuk National University, Jeonju 54896, Republic of Korea.
Yongseok ChoiSchool of Life Sciences and Biotechnology, Korea University, Seoul 02841, Republic of Korea.
Sik-Won ChoiForest Biomaterials Research Center, National Institute of Forest Science (NIFoS), Jinju 52817, Republic of Korea.ORCID 0000-0003-1726-2536

Funding

the Forest Biomaterials Research Center of the National Institute of Forest Science FP0400-2022-01-2024
6 · The paper itself

Abstract

Tumor cells in hypoxic conditions control cancer metabolism and angiogenesis by expressing HIF-1α. Tanshinone is a traditional Chinese medicine that has been shown to possess antitumor properties and exerts a therapeutic impact on angiogenesis. However, the precise molecular mechanism responsible for the antitumor activity of 3-Hydroxytanshinone (3-HT), a type of tanshinone, has not been fully understood. Therefore, our study aimed to investigate the mechanism by which 3-HT regulates the expression of HIF-1α. Our findings demonstrate that 3-HT inhibits HIF-1α activity and expression under hypoxic conditions. Additionally, 3-HT inhibits hypoxia-induced angiogenesis by suppressing the expression of VEGF. Moreover, 3-HT was found to directly bind to α-enolase, an enzyme associated with glycolysis, resulting in the suppression of its activity. This inhibition of α-enolase activity by 3-HT leads to the blockade of the glycolytic pathway and a decrease in glycolysis products, ultimately altering HIF1-α expression. Furthermore, 3-HT negatively regulates the expression of HIF-1α by altering the phosphorylation of AMP-activated protein kinase (AMPK). Our study's findings elucidate the mechanism by which 3-HT regulates HIF-1α through the inhibition of the glycolytic enzyme α-enolase and the phosphorylation of AMPK. These results suggest that 3-HT holds promise as a potential therapeutic agent for hypoxia-related angiogenesis and tumorigenesis.

Indexed as

GlycolysisHypoxia-Inducible Factor 1, alpha SubunitPhosphopyruvate HydrataseAbietanesCell HypoxiaCell Line, TumorHumansHuman Umbilical Vein Endothelial CellsNeovascularization, PathologicVascular Endothelial Growth Factor AAbietanesHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitPhosphopyruvate HydratasetanshinoneVascular Endothelial Growth Factor A3-HydroxytanshinoneglycolysisHIF-1αhypoxiaα-enolase

Identifiers

PMID38792080
PMCPMC11123766

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.