Evidence map›Paper›PMID 24954011›Full record

ReviewSeminars in cancer biology2014

Snail nuclear transport: the gateways regulating epithelial-to-mesenchymal transition?

Irfana Muqbil, Jack Wu, Amro Aboukameel, Ramzi M Mohammad, Asfar S Azmi

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in cancer biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
3.6field-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

55 citing papers in PubMed, 82 citations in OpenAlex.

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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

5 authors at 2 institutions in 2 countries.

Irfana MuqbilDepartment of Oncology, Karmanos Cancer Institute, USA.
Jack WuDepartment of Oncology, Karmanos Cancer Institute, USA.
Amro AboukameelDepartment of Oncology, Karmanos Cancer Institute, USA.
Ramzi M MohammadDepartment of Oncology, Karmanos Cancer Institute, USA; Division of Research, Hamad Medical Corporation, Doha, Qatar.
Asfar S AzmiDepartment of Pathology, Wayne State University, School of Medicine, Detroit, MI, USA. Electronic address: azmia@karmanos.org.
The Barbara Ann Karmanos Cancer Institute · USWayne State University · US

Funding

Differential Network Interrogations of Epithelial to Mesenchymal TransitionR21CA175974 · NCI · WAYNE STATE UNIVERSITY · PI MOHAMMAD, RAMZI M., REDDY, CHANDAN · 2013 to 2014
$359k
Development of Small Molecule Crm-1 Inhibitor for Pancreatic Cancer TherapyR21CA169848 · NCI · WAYNE STATE UNIVERSITY · PI MOHAMMAD, RAMZI M. · 2012 to 2013
$354k
NCI NIH HHS 1R21CA17597401NCI NIH HHS R21 1R21CA16984801NCI NIH HHS R21 CA169848NCI NIH HHS R21 CA175974
6 · The paper itself

Abstract

Epithelial-to-mesenchymal transition (EMT) and the reverse process (MET) play central role in organ developmental biology. It is a fine tuned process that when disturbed leads to pathological conditions especially cancers with aggressive and metastatic behavior. Snail is an oncogene that has been well established to be a promoter of EMT through direct repression of epithelial morphology promoter E-cadherin. It can function in the nucleus, in the cytosol and as discovered recently, extracellularly through secretory vesicular structures. The intracellular transport of snail has for long been shown to be regulated by the nuclear pore complex. One of the Karyopherins, importin alpha, mediates snail import, while exportin 1 (Xpo1) also known as chromosome maintenance region 1 (CRM1) is its major nuclear exporter. A number of additional biological regulators are emerging that directly modulate Snail stability by altering its subcellular localization. These observations indicate that targeting the nuclear transport machinery could be an important and as of yet, unexplored avenue for therapeutic intervention against the EMT processes in cancer. In parallel, a number of novel agents that disrupt nuclear transport have recently been discovered and are being explored for their anti-cancer effects in the early clinical settings. Through this review we provide insights on the mechanisms regulating snail subcellular localization and how this impacts EMT. We discuss strategies on how the nuclear transport function can be harnessed to rein in EMT through modulation of snail signaling.

Indexed as

Active Transport, Cell NucleusEpithelial-Mesenchymal TransitionAnimalsHumansNeoplasmsSnail Family Transcription FactorsTranscription FactorsSnail Family Transcription FactorsTranscription FactorsCRM1EMTKaryopherinNuclear transportXpo1

Identifiers

PMID24954011
PMCPMC4165636
OpenAlexW2055312095

What OpenQuestion holds

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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.