Evidence map›Paper›PMID 27485116›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Tumor suppressor Fbxw7 antagonizes WNT signaling by targeting β-catenin for degradation in pancreatic cancer.

Jian-Xin Jiang, Cheng-Yi Sun, She Tian, Chao Yu, Mei-Yuan Chen, Hao Zhang

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

  1. Review
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  11. SCFEMBO reports · 2022
    Article
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  14. Article
  15. Article
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  18. Dickkopf-4 gene expression is associated with differentiation and lymph node metastasis in colorectal cancer.JGH open : an open access journal of gastroenterology and hepatology · 2019
    Article
  19. Review
  20. Review
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

6 authors.

Jian-Xin JiangDepartment of Biliary-Hepatic SurgeryAffiliated Hospital of Guiyang Medical College, Guiyang, 550001, China.
Cheng-Yi SunDepartment of Biliary-Hepatic SurgeryAffiliated Hospital of Guiyang Medical College, Guiyang, 550001, China. chengyisun2014@163.com.
She TianDepartment of Biliary-Hepatic SurgeryAffiliated Hospital of Guiyang Medical College, Guiyang, 550001, China.
Chao YuDepartment of Biliary-Hepatic SurgeryAffiliated Hospital of Guiyang Medical College, Guiyang, 550001, China.
Mei-Yuan ChenDepartment of Biliary-Hepatic SurgeryAffiliated Hospital of Guiyang Medical College, Guiyang, 550001, China.
Hao ZhangDepartment of Biliary-Hepatic SurgeryAffiliated Hospital of Guiyang Medical College, Guiyang, 550001, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer is one of the deadliest solid malignancies associated with aberrant Wnt signaling activation. Fbxw7 mutations have been implicated in the development of pancreatic cancer, whereas the exact mechanism of this ubiquitin ligase as a tumor suppressor remains unclear in pancreatic carcinogenesis. Here, we describe that Fbxw7 is downregulated upon pancreatic cancer development. Depletion of Fbxw7 results in tumor suppression in pancreatic cancer cells, while Fbxw7 overexpression inhibits pancreatic cancer cell proliferation and invasion. Considering the negative correlation between Fbxw7 and β-catenin, we find that Fbxw7 antagonizes Wnt signaling through targeting β-catenin for its degradation. Moreover, the inhibitory effect of Fbxw7 on pancreatic cancer cell proliferation is mainly executed by the destruction of the Wnt/β-catenin signaling pathway. We also reveal that c-myc, a widely accepted target of Fbxw7, is also transcriptionally regulated by the Fbxw7/β-catenin axis in pancreatic cancer cells. Collectively, our results demonstrate that Fbxw7 is a novel regulator of Wnt/β-catenin signaling-dependent regulation of pancreatic cancer cell growth and invasion, and inactivation of Fbxw7 in pancreatic cancer tissues might be the reason for the aberrant activation of Wnt signaling.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsApoptosisbeta CateninBiomarkers, TumorBlotting, WesternCell Cycle ProteinsCell ProliferationF-Box ProteinsF-Box-WD Repeat-Containing Protein 7FemaleHumansImmunoprecipitationMiceMice, Inbred BALB CMice, Nudebeta CateninBiomarkers, TumorCell Cycle ProteinsCTNNB1 protein, humanF-Box ProteinsF-Box-WD Repeat-Containing Protein 7FBXW7 protein, humanRNA, MessengerUbiquitinUbiquitin-Protein LigasesWnt ProteinsDegradationFbxw7InteractionPancreatic cancerWnt/β-catenin

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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.