Evidence map›Paper›PMID 14965268›Full record

ReviewCurrent cancer drug targets2004

A dual role of cyclin E in cell proliferation and apoptosis may provide a target for cancer therapy.

S Mazumder, E L DuPree, A Almasan

Open access · greenAbstract readReview
In one paragraph

Review in Current cancer drug targets, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
2.5field-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

69 citing papers in PubMed, 127 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Styrylquinazoline derivatives as ABL inhibitors selective for different DFG orientations.Journal of enzyme inhibition and medicinal chemistry · 2023
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. The Pt(International journal of molecular sciences · 2022
    Article
  14. Article
  15. Molecular Patho-mechanisms of cervical cancer (MMP1).Annals of medicine and surgery (2012) · 2022
    Review
  16. Anti-cancer peptide-based therapeutic strategies in solid tumors.Cellular & molecular biology letters · 2022
    Article
  17. Article
  18. Article
  19. Article
  20. Cancers · 2021
    Article

9 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

3 authors at 2 institutions in 2 countries.

S MazumderDepartment of Cancer Biology, Lerner Research Institute, The Cleveland Clinic Foundation NB40, Cleveland, OH 44195, USA.
E L DuPree
A Almasan
Centre for Cancer Biology · AUCleveland State University · US

Funding

Signals for Commitment to Radiation Induces ApoptosisR01CA081504 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI ALMASAN, ALEXANDRU · 1999 to 2007
$1.6M
CYCLIN E AND GENOTOXIC STRESS INDUCED APOPTOSISR01CA082858 · NCI · CLEVELAND CLINIC FOUNDATION · PI ALMASAN, ALEXANDRU ALMASAN · 1999 to 2003
$818k
NCI NIH HHS CA 81504NCI NIH HHS CA 82858NCI NIH HHS R01 CA081504NCI NIH HHS R01 CA082858
6 · The paper itself

Abstract

Cyclin E is essential for progression through the G1-phase of the cell cycle and initiation of DNA replication by interacting with and activating its catalytic partner, the cyclin dependent kinase 2 (Cdk2). Rb, as well as Cdc6, NPAT, and nucleophosmin, critical components of cell proliferation and DNA replication, respectively, are targets of Cyclin E/Cdk2 phosphorylation. There are a number of putative binding sites for E2F in the cyclin E promoter region, suggesting an E2F-dependent regulation. Skp2 and Fbw7 are novel proteins, responsible for ubiquitin-dependent proteolysis of Cyclin E. The tight regulation of cyclin E expression, both at the transcriptional level and by ubiquitin-mediated proteolysis, indicates that it has a major role in the control of the G1- and S-phase transitions. Cyclin E is also transcriptionally regulated during radiation-induced apoptosis of hematopoietic cells. In addition to its biological roles, deregulated cyclin E expression has an established role in tumorigenesis. Cell cycle regulatory molecules, such as cyclin E, are frequently deregulated in different types of cancers, where overexpressed native or low molecular weight forms of Cyclin E have a significant role in oncogenesis. During apoptosis of hematopoietic cells, caspase-dependent proteolysis of Cyclin E generates a p18-Cyclin E variant. Understanding the role of Cyclin E in apoptosis may provide a novel target, which may be effective in cancer therapy. This review summarizes what is known about the biological role of cyclin E, its deregulation in cancer, and the opportunities it may provide as a target in clinical therapy.

Indexed as

Amino Acid SequenceAnimalsApoptosisCell DivisionCyclin EHumansMolecular Sequence DataNeoplasmsSequence Homology, Amino AcidCyclin E

Identifiers

PMID14965268
PMCPMC1307511
OpenAlexW2067776092

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.