Evidence map›Paper›PMID 26650241›Full record

ArticlePloS one2015

Hes1 Increases the Invasion Ability of Colorectal Cancer Cells via the STAT3-MMP14 Pathway.

M T Weng, P N Tsao, H L Lin, C C Tung, M C Change, Y T Chang, J M Wong, S C Wei

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 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 1 institution in 1 country.

M T WengDepartment of Internal Medicine, Far-Eastern Memorial Hospital, New Taipei, Taiwan.
P N TsaoDepartment of Pediatrics, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.
H L LinDepartment of Internal Medicine, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.
C C TungDepartment of Integrated Diagnostics & Therapeutics, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.
M C ChangeDepartment of Internal Medicine, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.
Y T ChangDepartment of Internal Medicine, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.
J M WongDepartment of Internal Medicine, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.
S C WeiDepartment of Internal Medicine, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.
National Taiwan University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Notch pathway contributes to self-renewal of tumor-initiating cell and inhibition of normal colonic epithelial cell differentiation. Deregulated expression of Notch1 and Jagged1 is observed in colorectal cancer. Hairy/enhancer of split (HES) family, the most characterized targets of Notch, involved in the development of many cancers. In this study, we explored the role of Hes1 in the tumorigenesis of colorectal cancer. Knocking down Hes1 induced CRC cell senescence and decreased the invasion ability, whereas over-expression of Hes1 increased STAT3 phosphorylation activity and up-regulated MMP14 protein level. We further explored the expression of Hes1 in human colorectal cancer and found high Hes1 mRNA expression is associated with poor prognosis in CRC patients. These findings suggest that Hes1 regulates the invasion ability through the STAT3-MMP14 pathway in CRC cells and high Hes1 expression is a predictor of poor prognosis of CRC.

Indexed as

Cellular SenescenceColorectal NeoplasmsHumansMatrix Metalloproteinase 14Neoplasm InvasivenessPhosphorylationSignal TransductionSTAT3 Transcription FactorTranscription Factor HES-1Up-RegulationHES1 protein, humanMatrix Metalloproteinase 14MMP14 protein, humanSTAT3 protein, humanSTAT3 Transcription FactorTranscription Factor HES-1

Identifiers

PMID26650241
PMCPMC4674118
OpenAlexW2190442201

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.