Evidence map›Paper›PMID 10454591›Full record

ArticleMolecular and cellular biology1999

Disruption of retinoblastoma protein family function by human papillomavirus type 16 E7 oncoprotein inhibits lens development in part through E2F-1.

J McCaffrey, L Yamasaki, N J Dyson, E Harlow, A E Griep

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.1field-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

17 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Review
  3. Cell Cycle Proteins as Key Regulators of Postmitotic Cell Death.The Yale journal of biology and medicine · 2019
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Cell cycle regulation in the developing lens.Seminars in cell & developmental biology · 2006
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

5 authors at 2 institutions in 1 country.

J McCaffreyDepartment of Anatomy, University of Wisconsin Medical School, Madison, Wisconsin 53706, USA.
L Yamasaki
N J Dyson
E Harlow
A E Griep
Massachusetts General Hospital · USUniversity of Wisconsin–Madison · US

Funding

Regulation of Ocular Lens Development by PDZ ProteinsR01EY009091 · NEI · UNIVERSITY OF WISCONSIN-MADISON · PI GRIEP, ANNE E · 1992 to 2011
$5.3M
RB-DEPENDENT PATHWAYS AND MURINE LENS DEVF32EY006709 · NEI · UNIVERSITY OF WISCONSIN MADISON · PI MCCAFFREY, JENNIFER · 1995 to 1997
–
NEI NIH HHS F32 EY006709NEI NIH HHS F32-EY06709NEI NIH HHS R01 EY009091NEI NIH HHS R01-EY09091
6 · The paper itself

Abstract

Complexes between the retinoblastoma protein (pRb) and the transcription factor E2F-1 are thought to be important for regulating cell proliferation. We have shown previously that the E7 oncoprotein from human papillomavirus type 16, dependent upon its binding to pRb proteins, induces proliferation, disrupts differentiation, and induces apoptosis when expressed in the differentiating, or fiber, cells of the ocular lenses in transgenic mice. Mice that carry a null mutation in E2F-1 do not exhibit any defects in proliferation and differentiation in the lens. By examining the lens phenotype in mice that express E7 on an E2F-1 null background, we now show genetic evidence that E7's ability to alter the fate of fiber cells is partially dependent on E2F-1. On the other hand, E2F-1 status does not affect E7-induced proliferation in the undifferentiated lens epithelium. These data provide genetic evidence that E2F-1, while dispensible for normal fiber cell differentiation, is one mediator of E7's activity in vivo and that the requirement for E2F-1 is context dependent. These data suggest that an important role for pRb-E2F-1 complex during fiber cell differentiation is to negatively regulate cell cycle progression, thereby allowing completion of the differentiation program to occur.

Indexed as

Carrier ProteinsCell Cycle ProteinsDNA-Binding ProteinsAnimalsAnimals, NewbornApoptosisCell CycleCell DifferentiationCell DivisionDNAE2F1 Transcription FactorE2F Transcription FactorsFemaleHumansLens, CrystallineMiceArid4a protein, mouseCarrier ProteinsCell Cycle ProteinsDNADNA-Binding ProteinsE2F1 protein, humanE2f1 protein, mouseE2F1 Transcription FactorE2F Transcription FactorsNuclear Proteinsoncogene protein E7, Human papillomavirus type 16Oncogene Proteins, ViralPapillomavirus E7 ProteinsRetinoblastoma-Binding Protein 1Transcription Factor DP1Transcription Factors

Identifiers

PMID10454591
PMCPMC84615
OpenAlexW2158269177

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.