Evidence map›Paper›PMID 20236126›Full record

ReviewClinical genetics2010

Conquering the complex world of human septins: implications for health and disease.

E A Peterson, E M Petty

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

66 citing papers in PubMed, 133 citations in OpenAlex.

  1. Article
  2. Review
  3. Local RhoA activation induces septin recruitment.bioRxiv : the preprint server for biology · 2025
    Article
  4. Pre-TreatmentCancers · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Detection of free DNA septin 9 gene methylation in plasma.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2021
    Article
  14. Animal reproduction · 2021
    Article
  15. Review
  16. Article
  17. Frontiers in oncology · 2021
    Article
  18. Article
  19. The Structural Biology of Septins and Their Filaments: An Update.Frontiers in cell and developmental biology · 2021
    Review
  20. Article

6 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

2 authors at 1 institution in 1 country.

E A PetersonDepartment of Human Genetics, University of Michigan Medical School, Ann Arbor, MI, USA.
E M Petty
University of Michigan–Ann Arbor · US

Funding

PREDOCTORAL TRAINING IN GENETICST32GM007544 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MORAN, JOHN V. · 1985 to 2022
$11.3M
The role of SEPT9 in cell proliferation and oncogenesisR01CA072877 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PETTY, ELIZABETH M. · 1997 to 2010
$2.4M
The role of SEPT9_v1 in mammary tumorigenesisF31CA123639 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PETERSON, ESTHER A · 2007 to 2009
$63k
NCI NIH HHS 5F31CA12363902NCI NIH HHS F31 CA123639NCI NIH HHS R01 CA072877NCI NIH HHS R01CA072877NIGMS NIH HHS T32 GM007544
6 · The paper itself

Abstract

Septins are highly conserved filamentous proteins first characterized in budding yeast and subsequently identified in must eukaryotes. Septins can bind and hydrolyze GTP, which is intrinsically related to their formation of septin hexamers and functional protein interactions. The human septin family is composed of 14 loci, SEPT1-SEPT14, which encode dozens of different septin proteins. Their central GTPase and polybasic domain regions are highly conserved but they diverge in their N-terminus and/or C-terminus. The mechanism by which the different isoforms are generated is not yet well understood, but one can hypothesize that the use of different promoters and/or alternative splicing could give rise to these variants. Septins perform diverse cellular functions according to tissue expression and their interacting partners. Functions identified to date include cell division, chromosome segregation, protein scaffolding, cellular polarity, motility, membrane dynamics, vesicle trafficking, exocytosis, apoptosis, and DNA damage response. Their expression is tightly regulated to maintain proper filament assembly and normal cellular functions. Alterations of these proteins, by mutation or expression changes, have been associated with a variety of cancers and neurological diseases. The association of septins with cancer results from alterations of expression in solid tumors or translocations in leukemias [mixed lineage leukemia (MLL)]. Expression changes in septins have also been associated with neurological conditions such as Alzheimer's and Parkinson's disease, as well as retinopathies, hepatitis C, spermatogenesis and Listeria infection. Pathogenic mutations of SEPT9 were identified in the autosomal dominant neurological disorder hereditary neuralgic amyotrophy (HNA). Human septin research over the past decade has established their importance in cell biology and human disease. Further functional characterization of septins is crucial to our understanding of their possible diagnostic, prognostic, and therapeutic applications.

Indexed as

Alzheimer DiseaseAmino Acid SequenceDiseaseGTP-Binding ProteinsHumansMolecular Sequence DataMutationNeoplasmsNervous System DiseasesPhylogenyGTP-Binding Proteins

Identifiers

PMID20236126
PMCPMC5087971
OpenAlexW2053719629

What OpenQuestion holds

Textmetadata
LicenceTDM
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.