Evidence map›Paper›PMID 25728752›Full record

ArticleMolecules and cells2015

Cell Proliferation and Motility Are Inhibited by G1 Phase Arrest in 15-kDa Selenoprotein-Deficient Chang Liver Cells.

Jeyoung Bang, Jang Hoe Huh, Ji-Woon Na, Qiao Lu, Bradley A Carlson, Ryuta Tobe, Petra A Tsuji, Vadim N Gladyshev, Dolph L Hatfield, Byeong Jae Lee

Open access · diamondAbstract read
In one paragraph

Article in Molecules and cells, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. "Alphabet" Selenoproteins: Their Characteristics and Physiological Roles.International journal of molecular sciences · 2023
    Review
  3. "Alphabet" Selenoproteins: Implications in Pathology.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Magnolol pretreatment attenuates heat stress-induced IEC-6 cell injury.Journal of Zhejiang University. Science. B · 2016
    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

10 authors at 3 institutions in 2 countries.

Jeyoung BangSchool of Biological Sciences, Seoul National University, Seoul, 151-742 Korea.
Jang Hoe HuhSchool of Biological Sciences, Seoul National University, Seoul, 151-742 Korea.
Ji-Woon NaSchool of Biological Sciences, Seoul National University, Seoul, 151-742 Korea.
Qiao LuSchool of Biological Sciences, Seoul National University, Seoul, 151-742 Korea.
Bradley A CarlsonMouse Cancer Genetics Program, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Ryuta TobeMouse Cancer Genetics Program, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Petra A TsujiDepartment of Biological Sciences, Towson University, Towson, MD 21252.
Vadim N GladyshevBrigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Dolph L HatfieldMouse Cancer Genetics Program, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Byeong Jae LeeSchool of Biological Sciences, Seoul National University, Seoul, 151-742 Korea.
Seoul National University · KRHarvard University · USTowson University · US

Funding

Selenoproteins as Targets for Cancer PreventionR01CA080946 · NCI · UNIVERSITY OF NEBRASKA LINCOLN · PI GLADYSHEV, VADIM N. · 2001 to 2018
$4.5M
Selenium in Health and its incorporation into Protein as SelenocysteineZIABC011620 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HATFIELD, DOLPH · 2015 to 2016
$587k
Intramural NIH HHSNCI NIH HHS CA080946NCI NIH HHS NIH CA080946NCI NIH HHS R01 CA080946
6 · The paper itself

Abstract

The 15-kDa selenoprotein (Sep15) is a selenoprotein residing in the lumen of the endoplasmic reticulum (ER) and implicated in quality control of protein folding. Herein, we established an inducible RNAi cell line that targets Sep15 mRNA in Chang liver cells. RNAi-induced Sep15 deficiency led to inhibition of cell proliferation, whereas cell growth was resumed after removal of the knockdown inducer. Sep15-deficient cells were arrested at the G1 phase by upregulating p21 and p27, and these cells were also characterized by ER stress. In addition, Sep15 deficiency led to the relocation of focal adhesions to the periphery of the cell basement and to the decrease of the migratory and invasive ability. All these changes were reversible depending on Sep15 status. Rescuing the knockdown state by expressing a silent mutant Sep15 mRNA that is resistant to siRNA also reversed the phenotypic changes. Our results suggest that SEP15 plays important roles in the regulation of the G1 phase during the cell cycle as well as in cell motility in Chang liver cells, and that this selenoprotein offers a novel functional link between the cell cycle and cell motility.

Indexed as

G1 PhaseCell LineCell MovementCell ProliferationHumansRNA, Small InterferingSelenoproteinsRNA, Small InterferingSELENOF protein, humanSelenoproteins15-kDa selenoproteincell cycle arrestcell proliferationcyclin Eselenium

Identifiers

PMID25728752
PMCPMC4443288
OpenAlexW1854904450

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.