Evidence map›Paper›PMID 30370649›Full record

ArticleCancer medicine2018

Focal adhesion kinase activation limits efficacy of Dasatinib in c-Myc driven hepatocellular carcinoma.

Xianqiong Liu, Xinhua Song, Jie Zhang, Zhong Xu, Li Che, Yu Qiao, Yunuen Ortiz Pedraza, Antonio Cigliano, Rosa M Pascale, Diego F Calvisi and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
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

12 authors at 5 institutions in 6 countries.

Xianqiong LiuSchool of Pharmacy, Hubei University of Chinese Medicine, Wuhan, Hubei, China.
Xinhua SongDepartment of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, California.
Jie ZhangDepartment of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, California.
Zhong XuDepartment of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, California.
Li CheDepartment of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, California.
Yu QiaoDepartment of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, California.
Yunuen Ortiz PedrazaDepartment of Bioengineering and Therapeutic Sciences and Liver Center, University of California, San Francisco, California.
Antonio CiglianoInstitute of Pathology, University of Greifswald, Greifswald, Germany.
Rosa M PascaleDepartment of Clinical and Experimental Medicine, University of Sassari, Sassari, Italy.
Diego F CalvisiInstitute of Pathology, University of Greifswald, Greifswald, Germany.
Yanju LiuSchool of Pharmacy, Hubei University of Chinese Medicine, Wuhan, Hubei, China.
Xin ChenSchool of Pharmacy, Hubei University of Chinese Medicine, Wuhan, Hubei, China.ORCID 0000-0002-9588-0164
University of California, San Francisco · USUniversity of Sassari · ITGuiyang Medical University · CNHubei University of Chinese Medicine · CNUniversitätsmedizin Greifswald · DE

Funding

UCSF Liver Core CenterP30DK026743 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Holger Willenbring · 1986 to 2026
$30.7M
Molecular Genetics of Liver CancersR01CA136606 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHEN, XIN · 2009 to 2016
$2.6M
Signaling cascades in cholangiocarcinoma developmentR01CA190606 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHEN, XIN · 2016 to 2020
$1.8M
Glutamine catabolism in c-Myc driven liver tumor developmentR21CA198490 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHEN, XIN · 2015 to 2016
$379k
NCI NIH HHS R01 CA136606NCI NIH HHS R01 CA190606NCI NIH HHS R21 CA198490NIDDK NIH HHS P30 DK026743
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a deadly malignancy with limited treatment options. Recently, it was found that Dasatinib treatment led to synthetic lethality in c-Myc high-expressing human cancer cells due to inhibition of p-Lyn. Overexpression of c-Myc is frequently seen in human HCC. We investigated the sensitivity to Dasatinib in vitro using HCC cell lines and in vivo using c-Myc mouse HCC model. We found that HCC cell line responsiveness to Dasatinib varied significantly. However, there was no correlation between c-Myc expression and IC

Indexed as

AnimalsAntineoplastic AgentsCarcinoma, HepatocellularCell Line, TumorDasatinibFemaleFocal Adhesion Protein-Tyrosine KinasesHumansLiver NeoplasmsMiceProtein Kinase InhibitorsProto-Oncogene Proteins c-mycAntineoplastic AgentsDasatinibFocal Adhesion Protein-Tyrosine KinasesProtein Kinase InhibitorsProto-Oncogene Proteins c-mycc-MycDasatinibfocal adhesion kinaseLynSrc

Identifiers

PMID30370649
PMCPMC6308083
OpenAlexW2899150764

What OpenQuestion holds

Textmetadata
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.