Evidence map›Paper›PMID 23236423›Full record

ArticlePloS one2012

Elevated expression of the serine-arginine protein kinase 1 gene in ovarian cancer and its role in Cisplatin cytotoxicity in vitro.

Kunle Odunsi, Paulette Mhawech-Fauceglia, Christopher Andrews, Amy Beck, Olajumoke Amuwo, Shashikant Lele, Jennifer D Black, Ruea-Yea Huang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
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  7. Review
  8. Frontiers in cellular and infection microbiology · 2022
    Article
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  19. The many faces of SRPK1.The Journal of pathology · 2017
    Article
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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

8 authors at 2 institutions in 1 country.

Kunle OdunsiDepartment of Gynecologic Oncology, Roswell Park Cancer Institute, Buffalo, New York, USA.
Paulette Mhawech-Fauceglia
Christopher Andrews
Amy Beck
Olajumoke Amuwo
Shashikant Lele
Jennifer D Black
Ruea-Yea Huang
Roswell Park Comprehensive Cancer Center · USUniversity at Buffalo, State University of New York · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI MARK G FRATTINI · 1985 to 2026
$116.6M
REGULATION OF CYCLIN D1 EXPRESSION IN THE INTESTINER01DK060632 · NIDDK · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BLACK, JENNIFER D. · 2002 to 2014
$2.6M
Regulation of cyclin D1 expression in the intestineR56DK060632 · NIDDK · ROSWELL PARK CANCER INSTITUTE CORP · PI BLACK, JENNIFER D. · 2009 to 2009
$373k
Identification of Novel Cisplatin Resistance GenesR21CA107303 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI HUANG, RUEA-YEA · 2004 to 2005
$325k
NCI NIH HHS CA 107303NCI NIH HHS CA16056NCI NIH HHS P30 CA016056NCI NIH HHS R21 CA107303NIDDK NIH HHS DK60632NIDDK NIH HHS R01 DK060632NIDDK NIH HHS R56 DK060632
6 · The paper itself

Abstract

Alternatively spliced variants of several oncogenes and tumor suppressors have been shown to be important for their tumorigenicity. In the present study we have tested whether serine-arginine protein kinase 1 (SRPK1), a major regulator of splicing factors, is involved in ovarian cancer progression and plays a role in chemo-sensitivity. By Western blot analyses, SRPK1 protein was found to be overexpressed in 4 out of 6 ovarian cancer cell lines as compared with an immortalized ovarian surface epithelial cell line; and in 55% of ovarian tumor samples as compared with non-neoplastic ovarian tissue samples. Reduction of SRPK1 expression using small interfering RNA (siRNA) encoding small hairpin RNA in ovarian cancer cells led to (i) reduced cell proliferation rate, slower cell cycle progression and compromised anchorage-independent growth and migration ability in vitro, (ii) decreased level of phosphorylation of multiple serine-arginine proteins, and P44/42MAPK and AKT proteins, and (iii) enhanced sensitivity to cisplatin. Together, these results suggest that elevated SRPK1 expression may play a role in ovarian tumorigenesis and SRPK1 may be a potential target for ovarian cancer therapy.

Indexed as

Antineoplastic AgentsApoptosisCarcinomaCell CycleCell Line, TumorCell ProliferationCell Transformation, NeoplasticCisplatinCytotoxinsFemaleGene Expression Regulation, NeoplasticHumansOvarian NeoplasmsPhosphorylationProtein Serine-Threonine KinasesRNA, Small InterferingAntineoplastic AgentsCisplatinCytotoxinsProtein Serine-Threonine KinasesRNA, Small InterferingSRPK1 protein, human

Identifiers

PMID23236423
PMCPMC3517604
OpenAlexW1991142042

What OpenQuestion holds

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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.