Evidence map›Paper›PMID 25405367›Full record

ReviewInternational journal of oncology2015

Role of the staphylococcal nuclease and tudor domain containing 1 in oncogenesis (review).

Nidhi Jariwala, Devaraja Rajasekaran, Jyoti Srivastava, Rachel Gredler, Maaged A Akiel, Chadia L Robertson, Luni Emdad, Paul B Fisher, Devanand Sarkar

Open access · hybridAbstract readReview
In one paragraph

Review in International journal of oncology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

46 citing papers in PubMed, 70 citations in OpenAlex.

  1. Review
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  12. Review
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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

9 authors at 1 institution in 1 country.

Nidhi JariwalaDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Devaraja RajasekaranDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Jyoti SrivastavaDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Rachel GredlerDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Maaged A AkielDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Chadia L RobertsonDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Luni EmdadDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Paul B FisherDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Devanand SarkarDepartment of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA, USA.
Virginia Commonwealth University · US

Funding

Training Grant in Digestive Diseases and Liver DiseasesT32DK007150 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI SANYAL, ARUN J · 1986 to 2017
$4.2M
Analysis of a novel regulator of hepatocellular carcinomaR01CA138540 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI SARKAR, DEVANAND · 2010 to 2014
$1.6M
AEG-1: Novel Gene Involved in Malignant GliomaR01CA134721 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI FISHER, PAUL B · 2009 to 2013
$1.5M
A novel mediator of obesity associated hepatocellular carcinoma (HCC)R21CA183954 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI SARKAR, DEVANAND · 2014 to 2015
$365k
NCI NIH HHS R01 CA134721NCI NIH HHS R01 CA138540NCI NIH HHS R21 CA183954NIDDK NIH HHS T32 DK007150
6 · The paper itself

Abstract

The staphylococcal nuclease and tudor domain containing 1 (SND1) is a multifunctional protein overexpressed in breast, prostate, colorectal and hepatocellular carcinomas and malignant glioma. Molecular studies have revealed the multifaceted activities of SND1 involved in regulating gene expression at transcriptional as well as post-transcriptional levels. Early studies identified SND1 as a transcriptional co-activator. SND1 is also a component of RNA-induced silencing complex (RISC) thus mediating RNAi function, a regulator of mRNA splicing, editing and stability, and plays a role in maintenance of cell viability. Such diverse actions allow the SND1 to modulate a complex array of molecular networks, thereby promoting carcinogenesis. Here, we describe the crucial role of SND1 in cancer development and progression, and highlight SND1 as a potential target for therapeutic intervention.

Indexed as

CarboxypeptidasesCell Transformation, NeoplasticEndonucleasesGene Expression Regulation, NeoplasticHumansMolecular Targeted TherapyNeoplasmsNuclear ProteinsRNA InterferenceRNA SplicingCarboxypeptidasesEndonucleasesNuclear ProteinsSCPEP1 protein, humanSND1 protein, human

Identifiers

PMID25405367
PMCPMC4277250
OpenAlexW2013151542

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.