Evidence map›Paper›PMID 36179047›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

FGFR redundancy limits the efficacy of FGFR4-selective inhibitors in hepatocellular carcinoma.

Zhanchao Tao, Yue Cui, Xilong Xu, Ting Han

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. 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
2.4field-weighted citation impact, top 10% 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, 29 citations in OpenAlex.

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  11. [Current status and new advancements in molecular imaging of liver cancer].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2024
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  14. Frequent loss ofiScience · 2024
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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

4 authors at 2 institutions in 1 country.

Zhanchao TaoGraduate School of Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China 100730.ORCID 0000-0002-2659-8632
Yue CuiNational Institute of Biological Sciences, Beijing, China 102206.ORCID 0000-0002-1338-4598
Xilong XuNational Institute of Biological Sciences, Beijing, China 102206.
Ting HanGraduate School of Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China 100730.ORCID 0000-0003-3168-8699
Beijing Normal University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant fibroblast growth factor 19 (FGF19) signaling mediated by its receptor, FGF receptor 4 (FGFR4), and coreceptor, klotho β (KLB), is a driver of hepatocellular carcinoma (HCC). Several potent FGFR4-selective inhibitors have been developed but have exhibited limited efficacy in HCC clinical trials. Here, by using HCC cell line models from the Cancer Cell Line Encyclopedia (CCLE) and the Liver Cancer Model Repository (LIMORE), we show that selective FGFR4 inactivation was not sufficient to inhibit cancer cell proliferation and tumor growth in FGF19-positive HCC. Moreover, genetic inactivation of

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsCell Line, TumorCell ProliferationFibroblast Growth FactorsHumansProtein Kinase InhibitorsReceptor, Fibroblast Growth Factor, Type 4FGFR4 protein, humanFibroblast Growth FactorsProtein Kinase InhibitorsReceptor, Fibroblast Growth Factor, Type 4FGF19FGFR4FGFR inhibitorHCCKLB

Identifiers

PMID36179047
PMCPMC9546626
OpenAlexW4298126050

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.