Evidence map›Paper›PMID 27966538›Full record

ArticleNature communications2016

NQO1 inhibits proteasome-mediated degradation of HIF-1α.

Eun-Taex Oh, Jung-Whan Kim, Joon Mee Kim, Soo Jung Kim, Jae-Seon Lee, Soon-Sun Hong, Justin Goodwin, Robin J Ruthenborg, Myung Gu Jung, Hae-June Lee and 4 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 4% 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

101 citing papers in PubMed, 1 synthesis or guideline pooled it, 166 citations in OpenAlex.

  1. Pooled it
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41 more citing papers are in PubMed but not listed here.

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

14 authors at 4 institutions in 2 countries.

Eun-Taex OhDepartment of Biomedical Sciences, College of Medicine, Inha University, Incheon 22212, Republic of Korea.
Jung-Whan KimDepartment of Biological Sciences, The University of Texas at Dallas, Richardson, Texas 75080, USA.
Joon Mee KimDepartment of Pathology, College of Medicine, Inha University, Incheon 400-712, Republic of Korea.
Soo Jung KimDepartment of Biomedical Sciences, College of Medicine, Inha University, Incheon 22212, Republic of Korea.
Jae-Seon LeeDepartment of Biomedical Sciences, College of Medicine, Inha University, Incheon 22212, Republic of Korea.ORCID http://orcid.org/0000-0001-6002-5267
Soon-Sun HongDepartment of Biomedical Sciences, College of Medicine, Inha University, Incheon 22212, Republic of Korea.
Justin GoodwinDepartment of Biological Sciences, The University of Texas at Dallas, Richardson, Texas 75080, USA.
Robin J RuthenborgDepartment of Biological Sciences, The University of Texas at Dallas, Richardson, Texas 75080, USA.ORCID http://orcid.org/0000-0001-5542-6234
Myung Gu JungDivision of Radiation Effects, Korea Institute of Radiological and Medical Sciences, Seoul 139-706, Republic of Korea.
Hae-June LeeDivision of Radiation Effects, Korea Institute of Radiological and Medical Sciences, Seoul 139-706, Republic of Korea.
Chul-Ho LeeLaboratory Animal Center, Korea Research Institute of Bioscience and Biotechnology, Yuseong-gu, Daejeon 305-806, Republic of Korea.
Eun Sung ParkHypoxia-related Disease Research Center, College of Medicine, Inha University, Incheon 22212, Republic of Korea.
Chulhee KimDepartment of Polymer Science and Engineering, Inha University, Incheon 22212, Republic of Korea.
Heon Joo ParkHypoxia-related Disease Research Center, College of Medicine, Inha University, Incheon 22212, Republic of Korea.
Inha University · KRThe University of Texas at Dallas · USKorea Institute of Radiological and Medical Sciences · KRKorea Research Institute of Bioscience and Biotechnology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overexpression of NQO1 is associated with poor prognosis in human cancers including breast, colon, cervix, lung and pancreas. Yet, the molecular mechanisms underlying the pro-tumorigenic capacities of NQO1 have not been fully elucidated. Here we show a previously undescribed function for NQO1 in stabilizing HIF-1α, a master transcription factor of oxygen homeostasis that has been implicated in the survival, proliferation and malignant progression of cancers. We demonstrate that NQO1 directly binds to the oxygen-dependent domain of HIF-1α and inhibits the proteasome-mediated degradation of HIF-1α by preventing PHDs from interacting with HIF-1α. NQO1 knockdown in human colorectal and breast cancer cell lines suppresses HIF-1 signalling and tumour growth. Consistent with this pro-tumorigenic function for NQO1, high NQO1 expression levels correlate with increased HIF-1α expression and poor colorectal cancer patient survival. These results collectively reveal a function of NQO1 in the oxygen-sensing mechanism that regulates HIF-1α stability in cancers.

Indexed as

Breast NeoplasmsCell Line, TumorColorectal NeoplasmsGene Knockdown TechniquesHomeostasisHumansHypoxia-Inducible Factor 1, alpha SubunitNAD(P)H Dehydrogenase (Quinone)OxygenProteasome Endopeptidase ComplexProtein StabilityHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitNAD(P)H Dehydrogenase (Quinone)NQO1 protein, humanOxygenProteasome Endopeptidase Complex

Identifiers

PMID27966538
PMCPMC5171868
OpenAlexW2562940458

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.