Evidence map›Paper›PMID 23674690›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

End-binding proteins sensitize microtubules to the action of microtubule-targeting agents.

Renu Mohan, Eugene A Katrukha, Harinath Doodhi, Ihor Smal, Erik Meijering, Lukas C Kapitein, Michel O Steinmetz, Anna Akhmanova

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. 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
4.2field-weighted citation impact, top 6% 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, 111 citations in OpenAlex.

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  10. Phase separation of +TIP networks regulates microtubule dynamics.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  14. Theory of tip structure-dependent microtubule catastrophes and damage-induced microtubule rescues.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

8 authors at 3 institutions in 2 countries.

Renu MohanCell Biology, Faculty of Science, Utrecht University, 3584 CH, Utrecht, The Netherlands.
Eugene A Katrukha
Harinath Doodhi
Ihor Smal
Erik Meijering
Lukas C Kapitein
Michel O Steinmetz
Anna Akhmanova
Utrecht University · NLErasmus University Rotterdam · NLPaul Scherrer Institute · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microtubule-targeting agents (MTAs) are widely used for treatment of cancer and other diseases, and a detailed understanding of the mechanism of their action is important for the development of improved microtubule-directed therapies. Although there is a large body of data on the interactions of different MTAs with purified tubulin and microtubules, much less is known about how the effects of MTAs are modulated by microtubule-associated proteins. Among the regulatory factors with a potential to have a strong impact on MTA activity are the microtubule plus end-tracking proteins, which control multiple aspects of microtubule dynamic instability. Here, we reconstituted microtubule dynamics in vitro to investigate the influence of end-binding proteins (EBs), the core components of the microtubule plus end-tracking protein machinery, on the effects that MTAs exert on microtubule plus-end growth. We found that EBs promote microtubule catastrophe induction in the presence of all MTAs tested. Analysis of microtubule growth times supported the view that catastrophes are microtubule age dependent. This analysis indicated that MTAs affect microtubule aging in multiple ways: destabilizing MTAs, such as colchicine and vinblastine, accelerate aging in an EB-dependent manner, whereas stabilizing MTAs, such as paclitaxel and peloruside A, induce not only catastrophes but also rescues and can reverse the aging process.

Indexed as

Models, BiologicalBridged Bicyclo Compounds, HeterocyclicCellular SenescenceColchicineDepsipeptidesGreen Fluorescent ProteinsHeLa CellsHumansLactonesMicroscopy, FluorescenceMicrotubule-Associated ProteinsMicrotubulesPaclitaxelPodophyllotoxinStatistics, NonparametricStilbenesBridged Bicyclo Compounds, HeterocyclicColchicineDepsipeptidesdolastatin 15fosbretabulinGreen Fluorescent ProteinsLactonesMicrotubule-Associated ProteinsPaclitaxelpeloruside APodophyllotoxinStilbenesTubulin ModulatorsVinblastineEB1EB3

Identifiers

PMID23674690
PMCPMC3670352
OpenAlexW2026682681

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.