Evidence map›Paper›PMID 30214242›Full record

ArticleOncoTargets and therapy2018

SRPK1 is a poor prognostic indicator and a novel potential therapeutic target for human colorectal cancer.

Nan Yi, Mingbing Xiao, Feng Jiang, Zhaoxiu Liu, Wenkai Ni, Cuihua Lu, Runzhou Ni, Weichang Chen

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 31% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 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

8 authors at 2 institutions in 1 country.

Nan YiDepartment of Gastroenterology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, People's Republic of China, weichangchensz@163.com.
Mingbing XiaoDepartment of Gastroenterology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, People's Republic of China, weichangchensz@163.com.
Feng JiangDepartment of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, People's Republic of China.
Zhaoxiu LiuDepartment of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, People's Republic of China.
Wenkai NiDepartment of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, People's Republic of China.
Cuihua LuDepartment of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, People's Republic of China.
Runzhou NiDepartment of Gastroenterology, Affiliated Hospital of Nantong University, Nantong, Jiangsu 226001, People's Republic of China.
Weichang ChenDepartment of Gastroenterology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, People's Republic of China, weichangchensz@163.com.
Nantong University · CNSoochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSerine/arginine protein kinase 1 (SRPK1) is a protein kinase that belongs to the serine/arginine-rich domain family of splicing factors which are essential for splice-site selection, especially the modulation for RNA metabolism, localization, and translation. High expression of SRPK1 has been found in numerous human cancers, but its mechanism in colorectal cancer (CRC) is still rarely reported. PURPOSE: To investigate the expression of SRPK1 in CRC tissues and cells and determine its functions and mechanism in CRC.

methodsThe expression of SRPK1 was explored in human CRC patients and cells by immunohistochemistry, real-time quantitative PCR, and Western blot; Cell Counting Kit-8, Transwell, flow cytometry, and tube formation assay were used to investigate the CRC cell viability, migration, apoptosis, and angiogenesis, respectively.

resultsSRPK1 was overexpressed in CRC tumor tissues and cells, and correlated with tumor node metastasis stage; inhibition of SRPK1 by siRNA resulted in decreased cell growth and migration, significantly increased apoptosis, and suppressed angiogenesis.

conclusionSRPK1 can be a prognostic indicator of CRC and may be a therapeutic target for CRC.

Indexed as

angiogenesisapoptosiscolorectal cancergrowthserine/arginine protein kinase 1

Identifiers

PMID30214242
PMCPMC6128266
OpenAlexW2889457844

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.