Evidence map›Paper›PMID 29851214›Full record

ArticleJournal of cellular and molecular medicine2018

In vitro and clinical data analysis of Osteopontin as a prognostic indicator in colorectal cancer.

Ran Wei, Janet Pik Ching Wong, Peng Lyu, Xinping Xi, Olivia Tong, Shu-Dong Zhang, Hiu Fung Yuen, Senji Shirasawa, Hang Fai Kwok

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
8.9field-weighted citation impact, top 2% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 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

9 authors at 4 institutions in 4 countries.

Ran WeiFaculty of Health Sciences, University of Macau, Taipa, Macau.
Janet Pik Ching WongFaculty of Health Sciences, University of Macau, Taipa, Macau.
Peng LyuFaculty of Health Sciences, University of Macau, Taipa, Macau.
Xinping XiFaculty of Health Sciences, University of Macau, Taipa, Macau.
Olivia TongFaculty of Health Sciences, University of Macau, Taipa, Macau.
Shu-Dong ZhangNorthern Ireland Centre for Stratified Medicine, Biomedical Sciences Research Institute, University of Ulster, Londonderry, UK.
Hiu Fung YuenInstitute of Molecular and Cell Biology, A*STAR, Singapore City, Singapore.
Senji ShirasawaDepartment of Cell Biology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Hang Fai KwokFaculty of Health Sciences, University of Macau, Taipa, Macau.ORCID 0000-0002-6349-4517
University of Macau · MOAgency for Science, Technology and Research · SGFukuoka University · JPUniversity of Ulster · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteopontin (OPN) has been shown to promote colorectal cancer (CRC) progression; however, the mechanism of OPN-induced CRC progression is largely unknown. In this study, we found that OPN overexpression led to enhanced anchorage-independent growth, cell migration and invasion in KRAS gene mutant cells but to a lesser extent in KRAS wild-type cells. OPN overexpression also induced PI3K signalling, expression of Snail and Matrix metallopeptidase 9 (MMP9), and suppressed the expression of E-cadherin in KRAS mutant cells. In human CRC specimens, a high-level expression of OPN significantly predicted poorer survival in CRC patients and OPN expression was positively correlated with MMP9 expression, and negatively correlated with E-cadherin expression. Furthermore, we have found that 15 genes were co-upregulated in OPN highly expression CRC and a list of candidate drugs that may have potential to reverse the secreted phosphoprotein 1 (SPP1) gene signature by connectivity mapping. In summary, OPN is a potential prognostic indicator and therapeutic target for colon cancer.

Indexed as

Gene Expression Regulation, NeoplasticAntigens, CDBiomarkers, TumorCadherinsCell Line, TumorCell MovementColorectal NeoplasmsDisease ProgressionHumansMatrix Metalloproteinase 9Neoplasm InvasivenessOsteopontinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins p21(ras)Signal TransductionSnail Family Transcription FactorsAntigens, CDBiomarkers, TumorCadherinsCDH1 protein, humanKRAS protein, humanMatrix Metalloproteinase 9MMP9 protein, humanOsteopontinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins p21(ras)SNAI1 protein, humanSnail Family Transcription FactorsSPP1 protein, humancolorectal cancerconnectivity mappingOsteopontinsurvival

Identifiers

PMID29851214
PMCPMC6111822
OpenAlexW2807282637

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.