Evidence map›Paper›PMID 22153075›Full record

ArticleCell2011

The STARD9/Kif16a kinesin associates with mitotic microtubules and regulates spindle pole assembly.

Jorge Z Torres, Matthew K Summers, David Peterson, Matthew J Brauer, James Lee, Silvia Senese, Ankur A Gholkar, Yu-Chen Lo, Xingye Lei, Kenneth Jung and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 12% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 83 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Involvement of kinesins in skeletal dysplasia: a review.American journal of physiology. Cell physiology · 2024
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Reduction in Absolute Neutrophil Counts in Patient on Clozapine Infected with COVID-19.International journal of environmental research and public health · 2021
    Review
  13. Article
  14. Article
  15. Phospho-regulation of mitotic spindle assembly.Cytoskeleton (Hoboken, N.J.) · 2020
    Review
  16. Article
  17. Article
  18. Dissecting the mechanisms of cell division.The Journal of biological chemistry · 2019
    Review
  19. 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

14 authors at 3 institutions in 1 country.

Jorge Z TorresDepartment of Pathology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA 94305, USA. torres@chem.ucla.edu
Matthew K Summers
David Peterson
Matthew J Brauer
James Lee
Silvia Senese
Ankur A Gholkar
Yu-Chen Lo
Xingye Lei
Kenneth Jung
David C Anderson
David P Davis
Lisa Belmont
Peter K Jackson
University of California, Los Angeles · USStanford University · USUniversity of Oregon · US

Funding

CYCLIN CONTROL OF DNA REPLICATIONR01GM054811 · NIGMS · STANFORD UNIVERSITY · PI JACKSON, PETER KENT · 1996 to 2005
$1.9M
Molecular Mechanisms of Drosophila Gonad MorphogenesisR01GM063023 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI VAN DOREN, MARK B · 2001 to 2005
$1.3M
NIGMS NIH HHS R01 GM054811NIGMS NIH HHS R01 GM063023
6 · The paper itself

Abstract

During cell division, cells form the microtubule-based mitotic spindle, a highly specialized and dynamic structure that mediates proper chromosome transmission to daughter cells. Cancer cells can show perturbed mitotic spindles and an approach in cancer treatment has been to trigger cell killing by targeting microtubule dynamics or spindle assembly. To identify and characterize proteins necessary for spindle assembly, and potential antimitotic targets, we performed a proteomic and genetic analysis of 592 mitotic microtubule copurifying proteins (MMCPs). Screening for regulators that affect both mitosis and apoptosis, we report the identification and characterization of STARD9, a kinesin-3 family member, which localizes to centrosomes and stabilizes the pericentriolar material (PCM). STARD9-depleted cells have fragmented PCM, form multipolar spindles, activate the spindle assembly checkpoint (SAC), arrest in mitosis, and undergo apoptosis. Interestingly, STARD9-depletion synergizes with the chemotherapeutic agent taxol to increase mitotic death, demonstrating that STARD9 is a mitotic kinesin and a potential antimitotic target.

Indexed as

ApoptosisMitosisAmino Acid SequenceCarrier ProteinsCell Line, TumorCentriolesHeLa CellsHumansMicrotubule ProteinsMicrotubulesMolecular Sequence DataNeoplasmsPhylogenyProteomeSequence AlignmentSpindle ApparatusCarrier ProteinsMicrotubule ProteinsProteomeSTARD9 protein, human

Identifiers

PMID22153075
PMCPMC4180425
OpenAlexW2031805768

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.