Evidence map›Paper›PMID 26621835›Full record

ArticleOncotarget2016

Negative correlation of ITCH E3 ubiquitin ligase and miRNA-106b dictates metastatic progression in pancreatic cancer.

Zhu-Lin Luo, Hui-Jun Luo, Chen Fang, Long Cheng, Zhu Huang, Ruiwu Dai, Kun Li, Fu-Zhou Tian, Tao Wang, Li-Jun Tang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

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  8. The Risks of miRNA Therapeutics: In a Drug Target Perspective.Drug design, development and therapy · 2021
    Review
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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 2 institutions in 2 countries.

Zhu-Lin LuoDepartment of General Surgery, Chengdu Military General Hospital, Chengdu, Sichuan 610083, P. R. China.
Hui-Jun LuoDepartment of Biochemistry and Molecular Biology, Mayo Clinic Arizona, Scottsdale, AZ 85259, USA.
Chen FangChengdu Military Institute for Drug and Instrument Control, Chengdu, Sichuan 610020, P. R. China.
Long ChengDepartment of General Surgery, Chengdu Military General Hospital, Chengdu, Sichuan 610083, P. R. China.
Zhu HuangDepartment of General Surgery, Chengdu Military General Hospital, Chengdu, Sichuan 610083, P. R. China.
Ruiwu DaiDepartment of General Surgery, Chengdu Military General Hospital, Chengdu, Sichuan 610083, P. R. China.
Kun LiMedical Central Laboratory, Chengdu Military General Hospital, Chengdu, Sichuan 610083, P. R. China.
Fu-Zhou TianDepartment of General Surgery, Chengdu Military General Hospital, Chengdu, Sichuan 610083, P. R. China.
Tao WangDepartment of General Surgery, Chengdu Military General Hospital, Chengdu, Sichuan 610083, P. R. China.
Li-Jun TangDepartment of General Surgery, Chengdu Military General Hospital, Chengdu, Sichuan 610083, P. R. China.
Chengdu Military General Hospital · CNMayo Clinic in Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer is one of the major malignancies and cause for mortality across the world, with recurrence and metastatic progression remaining the single largest cause of pancreatic cancer mortality. Hence it is imperative to develop novel biomarkers of pancreatic cancer prognosis. The E3 ubiquitin ligase ITCH has been previously reported to inhibit the tumor suppressive Hippo signaling by suppressing LATS1/2 in breast cancer and chronic lymphocytic leukemia. However, the role of ITCH in pancreatic cancer progression has not been described. Here we report that ITCH transcript and protein expression mimic metastatic trait in pancreatic cancer patients and cell lines. Loss-of-function studies of ITCH showed that the gene product is responsible for inducing metastasis in vivo. We furthermore show that hsa-miR-106b, which itself is down regulated in metastatic pancreatic cancer, directly interacts and inhibit ITCH expression. ITCH and hsa-miR-106b are thus potential biomarkers for pancreatic cancer prognosis.

Indexed as

Cell Movement3' Untranslated RegionsAnimalsBinding SitesBiomarkers, TumorCell Line, TumorFemaleGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticHeterograftsHumansKaplan-Meier EstimateMice, NudeMicroRNAsNeoplasm MetastasisPancreatic Neoplasms3' Untranslated RegionsBiomarkers, TumorITCH protein, humanMicroRNAsMIRN106 microRNA, humanRepressor ProteinsUbiquitin-Protein LigasesITCHmetastasismiR-106bpancreatic cancerYAP

Identifiers

PMID26621835
PMCPMC4811474
OpenAlexW2184586321

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.