Evidence map›Paper›PMID 12145320›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

Enhanced microtubule-dependent trafficking and p53 nuclear accumulation by suppression of microtubule dynamics.

Paraskevi Giannakakou, Michel Nakano, Kyriacos C Nicolaou, Aurora O'Brate, Jian Yu, Mikhail V Blagosklonny, Urs F Greber, Tito Fojo

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

81 citing papers in PubMed, 202 citations in OpenAlex.

  1. Article
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  10. Tirbanibulin for Actinic Keratosis: Insights into the Mechanism of Action.Clinical, cosmetic and investigational dermatology · 2022
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  15. Article
  16. Evaluation of Eribulin Combined with Irinotecan for Treatment of Pediatric Cancer Xenografts.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Article
  17. Article
  18. Review
  19. Article
  20. Article

21 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 1 institution in 1 country.

Paraskevi GiannakakouWinship Cancer Institute, Emory University School of Medicine, Atlanta, GA 30322, USA. paraskevi_giannakakou@emory.org
Michel Nakano
Kyriacos C Nicolaou
Aurora O'Brate
Jian Yu
Mikhail V Blagosklonny
Urs F Greber
Tito Fojo
National Cancer Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor suppressor protein p53 localizes to microtubules (MT) and, in response to DNA damage, is transported to the nucleus via the MT minus-end-directed motor protein dynein. Dynein is also responsible for MT-mediated nuclear targeting of adenovirus type 2 (Ad2). Here we show that treatment with low concentrations of MT-targeting compounds (MTCs) that do not disrupt the MT network but are known to suppress MT dynamics enhanced p53 nuclear accumulation, and the activation of the p53-downstream target genes. p53 nuclear accumulation required binding of MTCs to MTs and enhanced the induction of p53-up-regulated modulator of apoptosis (PUMA) mRNA and apoptosis on challenging cells with the DNA-damaging drug adriamycin. Low concentrations of MTCs enhanced the rate of movement of fluorescent Ad2 to the nucleus and increased the nuclear targeting efficiency of Ad2. We propose that suppression of MT dynamics by low concentrations of MTCs enhances MT-dependent trafficking toward the minus ends of MTs and facilitates nuclear targeting.

Indexed as

EpothilonesNuclear ProteinsAdenoviruses, HumanApoptosisBiological TransportCell NucleusColchicineDoxorubicinHeLa CellsHumansMacrolidesMicrotubulesNocodazolePaclitaxelProto-Oncogene ProteinsProto-Oncogene Proteins c-mdm2ColchicineDoxorubicinepothilone Aepothilone BEpothilonesMacrolidesMDM2 protein, humanNocodazoleNuclear ProteinsPaclitaxelProto-Oncogene ProteinsProto-Oncogene Proteins c-mdm2TubulinTumor Suppressor Protein p53Vincristine

Identifiers

PMID12145320
PMCPMC125062
OpenAlexW2042145670

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.