Evidence map›Paper›PMID 31195063›Full record

ArticleJournal of hepatology2019

Loss of Fbxw7 synergizes with activated Akt signaling to promote c-Myc dependent cholangiocarcinogenesis.

Jingxiao Wang, Haichuan Wang, Michele Peters, Ning Ding, Silvia Ribback, Kirsten Utpatel, Antonio Cigliano, Frank Dombrowski, Meng Xu, Xinyan Chen and 8 more

Open access · greenAbstract read
In one paragraph

Article in Journal of hepatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 2 pooled it
17.2field-weighted citation impact, top 1% 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

51 citing papers in PubMed, 2 syntheses or guidelines pooled it, 109 citations in OpenAlex.

  1. Guideline
  2. Molecular Targets and Signaling Pathways in Cholangiocarcinoma: A Systematic Review.Asian Pacific journal of cancer prevention : APJCP · 2023
    Pooled it
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  7. Co-repression ofbioRxiv : the preprint server for biology · 2026
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  14. Review
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  18. Transcriptional Up-Regulation of FBXW7 by KInternational journal of molecular sciences · 2024
    Article
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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

18 authors at 7 institutions in 4 countries.

Jingxiao WangSchool of Life Sciences, Beijing University of Chinese Medicine, Beijing, China; Department of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, CA, United States.
Haichuan WangDepartment of Liver Surgery, Liver Transplantation Division, West China Hospital, Sichuan University, Chengdu, China; Department of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, CA, United States; Laboratory of Liver Surgery, West China Hospital, Sichuan University, Chengdu, China.
Michele PetersInstitute of Pathology, University of Greifswald, Greifswald, Germany.
Ning DingDepartment of Gastroenterology, Beijing Chaoyang Hospital, Capital Medical University, Beijing, China.
Silvia RibbackInstitute of Pathology, University of Greifswald, Greifswald, Germany.
Kirsten UtpatelInstitute of Pathology, University of Regensburg, Regensburg, Germany.
Antonio CiglianoInstitute of Pathology, University of Greifswald, Greifswald, Germany; Institute of Pathology, University of Regensburg, Regensburg, Germany.
Frank DombrowskiInstitute of Pathology, University of Greifswald, Greifswald, Germany.
Meng XuDepartment of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, CA, United States; Department of General Surgery, The Second Hospital of Xi'an Jiaotong University, Xi'an Jiaotong University, Xi'an, China.
Xinyan ChenDepartment of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, CA, United States; Department of Pharmacy, Hubei University of Chinese Medicine, Wuhan, China.
Xinhua SongDepartment of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, CA, United States.
Li CheDepartment of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, CA, United States.
Matthias EvertInstitute of Pathology, University of Regensburg, Regensburg, Germany.
Antonio CossuUnit of Pathology, Azienda Ospedaliero Universitaria Sassari, Sassari, Italy.
John GordanDepartment of Medicine, University of California, San Francisco, CA, United States.
Yong ZengDepartment of Liver Surgery, Liver Transplantation Division, West China Hospital, Sichuan University, Chengdu, China; Laboratory of Liver Surgery, West China Hospital, Sichuan University, Chengdu, China. Electronic address: zengyong@medmail.com.cn.
Xin ChenDepartment of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, CA, United States. Electronic address: xin.chen@ucsf.edu.
Diego F CalvisiInstitute of Pathology, University of Greifswald, Greifswald, Germany; Institute of Pathology, University of Regensburg, Regensburg, Germany. Electronic address: diego.calvisi@klinik.uni-regensburg.de.
University of California, San Francisco · USUniversität Greifswald · DEUniversitätsmedizin Greifswald · DEAzienda Ospedaliero Universitaria di Sassari · ITBeijing University of Chinese Medicine · CNCapital Medical University · CNUniversity of Regensburg · DE

Funding

UCSF Liver Core CenterP30DK026743 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Holger Willenbring · 1986 to 2026
$30.7M
Role of Cancer-Associated Fibroblasts in CholangiocarcinomaR01CA228483 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHEN, XIN, SCHWABE, ROBERT F. · 2018 to 2022
$3.1M
Yap and beta-catenin interactions in liver: Implications in PathophysiologyR01CA204586 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHEN, XIN, MONGA, SATDARSHAN SINGH · 2016 to 2020
$2.1M
Signaling cascades in cholangiocarcinoma developmentR01CA190606 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHEN, XIN · 2016 to 2020
$1.8M
NCI NIH HHS R01 CA190606NCI NIH HHS R01 CA204586NCI NIH HHS R01 CA228483NIDDK NIH HHS P30 DK026743
6 · The paper itself

Abstract

BACKGROUND &

aimsThe ubiquitin ligase F-box and WD repeat domain-containing 7 (FBXW7) is recognized as a tumor suppressor in many cancer types due to its ability to promote the degradation of numerous oncogenic target proteins. Herein, we aimed to elucidate its role in intrahepatic cholangiocarcinoma (iCCA).

methodsHerein, we first confirmed that FBXW7 gene expression was reduced in human iCCA specimens. To identify the molecular mechanisms by which FBXW7 dysfunction promotes cholangiocarcinogenesis, we generated a mouse model by hydrodynamic tail vein injection of Fbxw7ΔF, a dominant negative form of Fbxw7, either alone or in association with an activated/myristylated form of AKT (myr-AKT). We then confirmed the role of c-MYC in human iCCA cell lines and its relationship to FBXW7 expression in human iCCA specimens.

resultsFBXW7 mRNA expression is almost ubiquitously downregulated in human iCCA specimens. While forced overexpression of Fbxw7ΔF alone did not induce any appreciable abnormality in the mouse liver, co-expression with AKT triggered cholangiocarcinogenesis and mice had to be euthanized by 15 weeks post-injection. At the molecular level, a strong induction of Fbxw7 canonical targets, including Yap, Notch2, and c-Myc oncoproteins, was detected. However, only c-MYC was consistently confirmed as a FBXW7 target in human CCA cell lines. Most importantly, selected ablation of c-Myc completely impaired iCCA formation in AKT/Fbxw7ΔF mice, whereas deletion of either Yap or Notch2 only delayed tumorigenesis in the same model. In human iCCA specimens, an inverse correlation between the expression levels of FBXW7 and c-MYC transcriptional activity was observed.

conclusionsDownregulation of FBXW7 is ubiquitous in human iCCA and cooperates with AKT to induce cholangiocarcinogenesis in mice via c-Myc-dependent mechanisms. Targeting c-MYC might represent an innovative therapy against iCCA exhibiting low FBXW7 expression. LAY SUMMARY: There is mounting evidence that FBXW7 functions as a tumor suppressor in many cancer types, including intrahepatic cholangiocarcinoma, through its ability to promote the degradation of numerous oncoproteins. Herein, we have shown that the low expression of FBXW7 is ubiquitous in human cholangiocarcinoma specimens. This low expression is correlated with increased c-MYC activity, leading to tumorigenesis. Our findings suggest that targeting c-MYC might be an effective treatment for intrahepatic cholangiocarcinoma.

Indexed as

CholangiocarcinomaLiver NeoplasmsAdaptor Proteins, Signal TransducingAnimalsCarcinogenesisCell Cycle ProteinsDisease Models, AnimalF-Box-WD Repeat-Containing Protein 7Genes, Tumor SuppressorHumansMiceMolecular Targeted TherapyProto-Oncogene Proteins c-mycReceptor, Notch2Signal TransductionTumor Cells, CulturedAdaptor Proteins, Signal TransducingCell Cycle ProteinsF-Box-WD Repeat-Containing Protein 7Fbxw7 protein, mouseMyc protein, mouseNotch2 protein, mouseProto-Oncogene Proteins c-mycReceptor, Notch2Yap1 protein, mouseYAP-Signaling ProteinsCholangiocarcinogenesisCholangiocarcinoma murine modelc-MycFBXW7Notch2Yap

Identifiers

PMID31195063
PMCPMC6773530
OpenAlexW2949088233

What OpenQuestion holds

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LicenceTDM
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.