Evidence map›Paper›PMID 26317792›Full record

ArticleOncotarget2015

Specificity protein (Sp) transcription factors and metformin regulate expression of the long non-coding RNA HULC.

Shruti U Gandhy, Parisa Imanirad, Un-Ho Jin, Vijayalekshmi Nair, Eric Hedrick, Yating Cheng, J Christopher Corton, KyoungHyun Kim, Stephen Safe

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 33 citations in OpenAlex.

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  13. Metformin and Breast Cancer: Molecular Targets.Journal of mammary gland biology and neoplasia · 2019
    Review
  14. Review
  15. Review
  16. HULC: an oncogenic long non-coding RNA in human cancer.Journal of cellular and molecular medicine · 2017
    Review
  17. Review
  18. Article
  19. Article
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

9 authors at 4 institutions in 1 country.

Shruti U GandhyInstitute of Biosciences and Technology, Texas A&M Health Sciences Center, Houston, TX, USA.
Parisa ImaniradDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, TX, USA.
Un-Ho JinInstitute of Biosciences and Technology, Texas A&M Health Sciences Center, Houston, TX, USA.
Vijayalekshmi NairDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, TX, USA.
Eric HedrickDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, TX, USA.
Yating ChengDepartment of Veterinary Physiology and Pharmacology, Texas A&M University, College Station, TX, USA.
J Christopher CortonIntegrated Systems Toxicology Division, US-EPA, MD B143-06, Research Triangle Park, NC, USA.
KyoungHyun KimDepartment of Environmental Health, University of Cincinnati, Cincinnati, OH, USA.
Stephen SafeInstitute of Biosciences and Technology, Texas A&M Health Sciences Center, Houston, TX, USA.
Texas A&M University · USTexas A&M Health Science Center · USEnvironmental Protection Agency · USUniversity of Cincinnati · US

Funding

TARGETED GENOMICS FACILITY COREP30ES023512 · NIEHS · TEXAS A&M AGRILIFE RESEARCH · PI THREADGILL, DAVID W. · 2014 to 2017
$3.3M
NIEHS NIH HHS P30 ES023512NIEHS NIH HHS P30-ES023512
6 · The paper itself

Abstract

Specificity protein 1 (Sp1) transcription factor (TF) regulates expression of long non-coding RNAs (lncRNAs) in hepatocellular carcinoma (HCC) cells. RNA interference (RNAi) studies showed that among several lncRNAs expressed in HepG2, SNU-449 and SK-Hep-1 cells, highly upregulated in liver cancer (HULC) was regulated not only by Sp1 but also Sp3 and Sp4 in the three cell lines. Knockdown of Sp transcription factors and HULC by RNAi showed that they play important roles in HCC cell proliferation, survival and migration. The relative contribution of Sp1, Sp3, Sp4 and HULC on these responses in HepG2, SNU-449 and SK-Hep-1 cells were cell context- and response-dependent. In the poorly differentiated SK-Hep-1 cells, knockdown of Sp1 or HULC resulted in genomic and morphological changes, indicating that Sp1 and Sp1-regulated HULC are important for maintaining the mesenchymal phenotype in this cell line. Genomic analysis showed an inverse correlation between expression of genes after knockdown of HULC and expression of those genes in liver tumors from patients. The antidiabetic drug metformin down-regulates Sp proteins in pancreatic cancer, and similar results including decreased HULC expression were observed in HepG2, SNU-449 and SK-Hep-1 cells treated with metformin, indicating that metformin and other antineoplastic agents that target Sp proteins may have clinical applications for HCC chemotherapy.

Indexed as

Antineoplastic AgentsCarcinoma, HepatocellularCell MovementCell ProliferationCell SurvivalDose-Response Relationship, DrugGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseHep G2 CellsHumansLiver NeoplasmsMetforminNeoplasm InvasivenessPhenotypeRNA InterferenceRNA, Long NoncodingAntineoplastic AgentsHULC long non-coding RNA, humanMetforminRNA, Long NoncodingSp Transcription FactorsHCCHULCIncRNAsSp proteins

Identifiers

PMID26317792
PMCPMC4694907
OpenAlexW1503579609

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.