Evidence map›Paper›PMID 30050307›Full record

ArticleOncoTargets and therapy2018

Expression of protein disulfide isomerase A3 precursor in colorectal cancer.

Zhaowei Yang, Juan Liu, Qinghong Shi, Yang Chao, Yanqing Di, Jing Sun, Jiebing Zhang, Lihong Huang, Honghua Guo, Chengyan He

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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 18 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

10 authors at 1 institution in 1 country.

Zhaowei YangLaboratory Medicine Center, China-Japan Union Hospital of Jilin University, Changchun, China, chengyanhe469@vip.sina.com.
Juan LiuDepartment of Digestive Internal Medicine, Qian Wei Hospital of Jilin Province, Changchun, China.
Qinghong ShiLaboratory Medicine Center, China-Japan Union Hospital of Jilin University, Changchun, China, chengyanhe469@vip.sina.com.
Yang ChaoDepartment of Digestive Internal Medicine, China-Japan Union Hospital of Jilin University, Changchun, China, guohonghua_2015@163.com.
Yanqing DiDepartment of Digestive Internal Medicine, China-Japan Union Hospital of Jilin University, Changchun, China, guohonghua_2015@163.com.
Jing SunDepartment of Digestive Internal Medicine, China-Japan Union Hospital of Jilin University, Changchun, China, guohonghua_2015@163.com.
Jiebing ZhangDepartment of Digestive Internal Medicine, China-Japan Union Hospital of Jilin University, Changchun, China, guohonghua_2015@163.com.
Lihong HuangDepartment of Geriatrics, China-Japan Union Hospital of Jilin University, Changchun, China.
Honghua GuoDepartment of Digestive Internal Medicine, China-Japan Union Hospital of Jilin University, Changchun, China, guohonghua_2015@163.com.
Chengyan HeLaboratory Medicine Center, China-Japan Union Hospital of Jilin University, Changchun, China, chengyanhe469@vip.sina.com.
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOver 20% of colorectal cancer (CRC) patients seek medical attention for the first time when they are in the advanced stages of CRC. Thus, early and reliable detection of CRC is critical to early diagnosis of CRC. Protein disulfide isomerase A3 precursor (PDIA3) has been implicated in various types of cancers. However, little is known about PDIA3 in CRC.

methodsIn this study, we screened PDIA3 expression in CRC tissues and cell lines. Small interfering RNA (siRNA) was introduced into SW480 cells to knockdown PDIA3 expression. The effect of PDIA3 in cell growth was evaluated.

resultsSignificant upregulation of PDIA3 expression was found in CRC tissues as compared with adjacent non-cancer tissues, and was found in established CRC cell lines (SW480, HCT116, CACO2, NCM460 and HT-29). In SW480 cells, knockdown of PDIA3 expression with siRNA resulted in subcellular morphological change, reduced cell proliferation and increased apoptosis.

conclusionPDIA3 inhibition could suppress CRC, likely through inducing apoptosis. PDIA3 could be a potential therapeutic target for CRC.

Indexed as

apoptosiscolorectal cancerPDIA3proteomicssiRNA

Identifiers

PMID30050307
PMCPMC6056171
OpenAlexW2884656252

What OpenQuestion holds

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Registered trials

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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.