Evidence map›Paper›PMID 12032846›Full record

ArticleOncogene2002

Human telomerase accelerates growth of lens epithelial cells through regulation of the genes mediating RB/E2F pathway.

Hua Xiang, Juan Wang, Yingwei Mao, Mingyao Liu, Venkat N Reddy, David Wan-Cheng Li

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

30 citing papers in PubMed, 86 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Non-canonical roles of canonical telomere binding proteins in cancers.Cellular and molecular life sciences : CMLS · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. MST-312 induces G2/M cell cycle arrest and apoptosis in APL cells through inhibition of telomerase activity and suppression of NF-κB pathway.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Sumoylation activates the transcriptional activity of Pax-6, an important transcription factor for eye and brain development.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  20. 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

6 authors at 3 institutions in 1 country.

Hua XiangDepartment of Molecular Biology, University of Medicine and Dentistry of New Jersey School of Osteopathic Medicine, Stratford, New Jersey, NJ 08084, USA.
Juan Wang
Yingwei Mao
Mingyao Liu
Venkat N Reddy
David Wan-Cheng Li
Rowan University · USTexas A&M University System · USUniversity of Michigan–Ann Arbor · US

Funding

STUDY OF INTRAOCULAR TRANSPORTR01EY000484 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI REDDY, VENKAT N · 1985 to 2004
$1.5M
APOPTOSIS--LENS DIFFERENTIATION AND CATARACT DEVELOPMENTR29EY011372 · NEI · UNIV OF MED/DENT NJ-SCH OSTEOPATHIC MED · PI LI, DAVID W · 1996 to 2000
$126k
STUDY OF INTRAOCULAR TRANSPORT AND METABOLISMR37EY000484 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI REDDY, VENKAT N · 1989 to 1998
–
NEI NIH HHS EY 00484NEI NIH HHS EY 07003NEI NIH HHS EY 11372
6 · The paper itself

Abstract

Telomerase is a specialized reverse transcriptase that extends telomeres of eukaryotic chromosomes. The catalytic core of human telomerase is composed of an RNA template known as hTER (human telomerase RNA) and a protein subunit named hTERT (human telomerase reverse transcriptase). We have been studying other functions of the telomerase besides its major role in telomere maintenance. In our previous work, we have demonstrated that the hTERT can functionally interact with a rabbit TER to regulate expression of other genes and also attenuate the induced apoptosis. Here we report that overexpression of hTERT in a human lens epithelial cell line accelerates growth of the transfected lens epithelial cells. Associated with the acceleration of cell growth, expression of p53, p21 and GCIP (Grap2 cyclin-D interacting protein) is downregulated in the hTERT-transfected cells. With the downregulation of p21 and GCIP, the retinoblastoma protein (RB) is completely hyperphosphorylated in the hTERT-transfected cells. As expected, in the presence of RB hyperphosphorylation, the E2F transactivity is upregulated. Inhibition of telomerase activity abolishes the observed growth acceleration and also the related molecular changes. Furthermore, expression of hTERT in telomerase-negative human lens epithelial cells derived from primary cultures also accelerates growth of the transfected cells. Taken together, our results suggest that hTERT, when overexpressed in human lens epithelial cells, accelerates cell growth rate through regulation of RB/E2F pathway and possibly other genes.

Indexed as

Cell Cycle ProteinsDNA-Binding ProteinsGene Expression RegulationSignal TransductionBlotting, WesternCell DivisionCell LineE2F Transcription FactorsEpithelial CellsHumansLens, CrystallinePhosphorylationRetinoblastoma ProteinReverse Transcriptase Polymerase Chain ReactionRNA, MessengerTelomeraseCell Cycle ProteinsDNA-Binding ProteinsE2F Transcription FactorsRetinoblastoma ProteinRNA, MessengerTelomeraseTranscription Factors

Identifiers

PMID12032846
OpenAlexW2325329824

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.