Evidence map›Paper›PMID 25659153›Full record

ArticlePloS one2015

Tanshinone IIA inhibits HIF-1α and VEGF expression in breast cancer cells via mTOR/p70S6K/RPS6/4E-BP1 signaling pathway.

Guobing Li, Changyu Shan, Lei Liu, Ting Zhou, Jing Zhou, Xiaoye Hu, Yibiao Chen, Hongjuan Cui, Ning Gao

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
27.1field-weighted citation impact, top 1% 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

53 citing papers in PubMed, 94 citations in OpenAlex.

  1. Effect of Moxibustion on HIF-1Pain research & management · 2019
    Trial
  2. Review
  3. Article
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  6. Review
  7. Article
  8. Review
  9. Article
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  15. Review
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  17. Frontiers in pharmacology · 2022
    Review
  18. Frontiers in pharmacology · 2022
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Guobing LiCollege of Pharmacy, Third Military Medical University, Chongqing, China.
Changyu ShanCollege of Pharmacy, Third Military Medical University, Chongqing, China.
Lei LiuCollege of Pharmacy, Third Military Medical University, Chongqing, China.
Ting ZhouCollege of Pharmacy, Third Military Medical University, Chongqing, China.
Jing ZhouCollege of Pharmacy, Third Military Medical University, Chongqing, China.
Xiaoye HuCollege of Pharmacy, Third Military Medical University, Chongqing, China.
Yibiao ChenState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.
Hongjuan CuiState Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing, China.
Ning GaoCollege of Pharmacy, Third Military Medical University, Chongqing, China.
Army Medical University · CNSouthwest University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypoxia-inducible factor 1α (HIF-1α) and vascular endothelial growth factor (VEGF) play important roles in angiogenesis and tumor growth. Tanshinone IIA (T2A) is a novel antiangiogenic agent with promising antitumor effects; however, the molecular mechanism underlying the antiangiogenic effects of T2A remains unclear. In the present study, we provided evidence showing that T2A inhibited angiogenesis and breast cancer growth by down-regulating VEGF expression. Specifically, T2A repressed HIF-1α expression at the translational level and inhibited the transcriptional activity of HIF-1α, which led to the down-regulation of VEGF expression. Suppression of HIF-1α synthesis by T2A correlated with strong dephosphorylation of mammalian target of rapamycin (mTOR) and its effectors ribosomal protein S6 kinase (p70S6K) and eukaryotic initiation factor 4E-binding protein-1 (4E-BP1), a pathway regulating HIF-1α expression at the translational level. In addition, we also found that T2A inhibited the angiogenesis and growth of human breast cancer xenografts in nude mice through suppression of HIF-1α and VEGF. Our study provides novel perspectives and potential targets for the treatment of human breast cancer.

Indexed as

AbietanesAdaptor Proteins, Signal TransducingAnimalsAntineoplastic Agents, PhytogenicBreast NeoplasmsCell Cycle ProteinsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansHypoxia-Inducible Factor 1, alpha SubunitMiceMice, NudeNeoplasm ProteinsNeovascularization, PathologicPhosphoproteinsAbietanesAdaptor Proteins, Signal TransducingAntineoplastic Agents, PhytogenicCell Cycle ProteinsEIF4EBP1 protein, humanHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMTOR protein, humanNeoplasm ProteinsPhosphoproteinsRibosomal Protein S6Ribosomal Protein S6 Kinases, 70-kDatanshinoneTOR Serine-Threonine KinasesVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID25659153
PMCPMC4320086
OpenAlexW2016580965

What OpenQuestion holds

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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.