Evidence map›Paper›PMID 24037088›Full record

ArticleCell death and differentiation2013

HINCUTs in cancer: hypoxia-induced noncoding ultraconserved transcripts.

J Ferdin, N Nishida, X Wu, M S Nicoloso, M Y Shah, C Devlin, H Ling, M Shimizu, K Kumar, M A Cortez and 13 more

Abstract read
In one paragraph

Article in Cell death and differentiation, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing 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

64 citing papers in PubMed.

  1. Review
  2. Article
  3. GANAB andInternational journal of molecular sciences · 2022
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Integrative Map ofGenes · 2021
    Article
  13. The Role of lncRNA in the Development of Tumors, including Breast Cancer.International journal of molecular sciences · 2021
    Review
  14. Hypoxia-Induced Non-Coding RNAs Controlling Cell Viability in Cancer.International journal of molecular sciences · 2021
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

4 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

23 authors.

J Ferdin1] Department of Experimental Therapeutics, The Center for RNA Interference and Non-Coding RNAs, MD Anderson Cancer Center, The University of Texas, So Campus Research Building 3, 1881 East Road, Houston, TX 77030, USA [2] Chair of Genetics, Animal Biotechnology and Immunology, Department of Animal Science, Biotechnical Faculty, University of Ljubljana, Groblje 3 1230, Domzale, Slovenia.
N Nishida
X Wu
M S Nicoloso
M Y Shah
C Devlin
H Ling
M Shimizu
K Kumar
M A Cortez
M Ferracin
Y Bi
D Yang
B Czerniak
W Zhang
T D Schmittgen
M P Voorhoeve
M J Reginato
M Negrini
R V Davuluri
T Kunej
M Ivan
G A Calin

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
University of Texas M.D. Anderson Cancer SPORE-LeukemiaP50CA100632 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KONOPLEVA, MARINA Y · 2003 to 2023
$43.7M
Targeting the p53 pathway for reversal of oral premalignancyP50CA097007 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MYERS, JEFFREY NICHOLAS · 2002 to 2012
$26.1M
Role of Hypoxia-Induced miR-210 in Tumor MetabolismR01CA155332 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI IVAN, MIRCEA · 2011 to 2015
$1.7M
Role of nutrient sensor O-GlcNAc transferase in regulating cancerR01CA155413 · NCI · DREXEL UNIVERSITY · PI REGINATO, MAURICIO J. · 2011 to 2015
$1.7M
MicroRNAs and other non-coding RNAs in Colorectal MetastasisR01CA135444 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI CALIN, GEORGE A., DAVULURI, RAMANA V · 2009 to 2010
$651k
NCI NIH HHS CA135444NCI NIH HHS CA16672NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA097007NCI NIH HHS P50 CA100632NCI NIH HHS R01 CA135444NCI NIH HHS R01 CA155332NCI NIH HHS R01 CA155332-01A1NCI NIH HHS R01 CA155413
6 · The paper itself

Abstract

Recent data have linked hypoxia, a classic feature of the tumor microenvironment, to the function of specific microRNAs (miRNAs); however, whether hypoxia affects other types of noncoding transcripts is currently unknown. Starting from a genome-wide expression profiling, we demonstrate for the first time a functional link between oxygen deprivation and the modulation of long noncoding transcripts from ultraconserved regions, termed transcribed-ultraconserved regions (T-UCRs). Interestingly, several hypoxia-upregulated T-UCRs, henceforth named 'hypoxia-induced noncoding ultraconserved transcripts' (HINCUTs), are also overexpressed in clinical samples from colon cancer patients. We show that these T-UCRs are predominantly nuclear and that the hypoxia-inducible factor (HIF) is at least partly responsible for the induction of several members of this group. One specific HINCUT, uc.475 (or HINCUT-1) is part of a retained intron of the host protein-coding gene, O-linked N-acetylglucosamine transferase, which is overexpressed in epithelial cancer types. Consistent with the hypothesis that T-UCRs have important function in tumor formation, HINCUT-1 supports cell proliferation specifically under hypoxic conditions and may be critical for optimal O-GlcNAcylation of proteins when oxygen tension is limiting. Our data gives a first glimpse of a novel functional hypoxic network comprising protein-coding transcripts and noncoding RNAs (ncRNAs) from the T-UCRs category.

Indexed as

Cell HypoxiaCell Line, TumorConserved SequenceDNA, NeoplasmDown-RegulationEnhancer Elements, GeneticGene Expression Regulation, NeoplasticGenetic LociHumansHypoxia-Inducible Factor 1, alpha SubunitN-AcetylglucosaminyltransferasesNeoplasmsReproducibility of ResultsRNA, MessengerRNA, UntranslatedTranscription, GeneticDNA, NeoplasmHypoxia-Inducible Factor 1, alpha SubunitN-AcetylglucosaminyltransferasesRNA, MessengerRNA, UntranslatedUDP-N-acetylglucosamine-peptide beta-N-acetylglucosaminyltransferase

Identifiers

PMID24037088
PMCPMC3824588

What OpenQuestion holds

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Registered trials

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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.