Evidence map›Paper›PMID 25973298›Full record

ArticleAmerican journal of cancer research2015

Minocycline attenuates hypoxia-inducible factor-1α expression correlated with modulation of p53 and AKT/mTOR/p70S6K/4E-BP1 pathway in ovarian cancer: in vitro and in vivo studies.

Parvin Ataie-Kachoie, Mohammad H Pourgholami, Farnaz Bahrami-B, Samina Badar, David L Morris

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

23 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  8. Review
  9. Theasaponin EMolecules (Basel, Switzerland) · 2021
    Article
  10. [Overexpression of lncRNA MEG3 inhibits proliferation and invasion of glioblastoma U251 cellsNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2021
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Biomedicines · 2019
    Review
  17. Review
  18. Article
  19. Article
  20. p53: key conductor of all anti-acne therapies.Journal of translational medicine · 2017
    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

5 authors at 2 institutions in 1 country.

Parvin Ataie-KachoieDepartment of Surgery, St George Hospital Sydney, Australia.
Mohammad H PourgholamiDepartment of Surgery, St George Hospital Sydney, Australia.
Farnaz Bahrami-BUniversity of New South Wales Department of Surgery, St George and Sutherland Clinical School Sydney, Australia.
Samina BadarUniversity of New South Wales Department of Surgery, St George and Sutherland Clinical School Sydney, Australia.
David L MorrisDepartment of Surgery, St George Hospital Sydney, Australia ; University of New South Wales Department of Surgery, St George and Sutherland Clinical School Sydney, Australia.
Sutherland Hospital · AUSt George Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypoxia-inducible factor (HIF)-1α is the key cellular survival protein under hypoxia, and is associated with tumor progression and angiogenesis. We have recently shown the inhibitory effects of minocycline on ovarian tumor growth correlated with attenuation of vascular endothelial growth factor (VEGF) and herein report a companion laboratory study to test if these effects were the result of HIF-1α inhibition. In vitro, human ovarian carcinoma cell lines (A2780, OVCAR-3 and SKOV-3) were utilized to examine the effect of minocycline on HIF-1 and its upstream pathway components to elucidate the underlying mechanism of action of minocycline. Mice harboring OVCAR-3 xenografts were treated with minocycline to assess the in vivo efficacy of minocycline in the context of HIF-1. Minocycline negatively regulated HIF-1α protein levels in a concentration-dependent manner and induced its degradation by a mechanism that is independent of prolyl-hydroxylation. The inhibition of HIF-1α was found to be associated with up-regulation of endogenous p53, a tumor suppressor with confirmed role in HIF-1α degradation. Further studies demonstrated that the effect of minocycline was not restricted to proteasomal degradation and that it also caused down-regulation of HIF-1α translation by suppressing the AKT/mTOR/p70S6K/4E-BP1 signaling pathway. Minocycline treatment of mice bearing established ovarian tumors, led to suppression of HIF-1α accompanied by up-regulation of p53 protein levels and inactivation of AKT/mTOR/p70S6K/4E-BP1 pathway. These data reveal the therapeutic potential of minocycline in ovarian cancer as an agent that targets the pro-oncogenic factor HIF-1α through multiple mechanisms.

Indexed as

AKTHIF-1MinocyclinemTORovarian cancerp53VEGF

Identifiers

PMID25973298
PMCPMC4396050
OpenAlexW2414984647

What OpenQuestion 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 OpenQuestion graph.