Evidence map›Paper›PMID 28122154›Full record

ArticleCancer science2017

Protein kinase A inhibition facilitates the antitumor activity of xanthohumol, a valosin-containing protein inhibitor.

Yuki Shikata, Tetsuro Yoshimaru, Masato Komatsu, Hiroto Katoh, Reiko Sato, Shuhei Kanagaki, Yasumasa Okazaki, Shinya Toyokuni, Etsu Tashiro, Shumpei Ishikawa and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Lipid metabolism reprogramming and its potential targets in cancer.Cancer communications (London, England) · 2018
    Review
  8. 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 4 institutions in 1 country.

Yuki ShikataDepartment of Biosciences and Informatics, Faculty of Science and Technology, Keio University, Yokohama, Japan.ORCID http://orcid.org/0000-0003-0203-1794
Tetsuro YoshimaruDivision of Genome Medicine, Institute for Genome Research, Tokushima University, Tokushima, Japan.
Masato KomatsuDivision of Genome Medicine, Institute for Genome Research, Tokushima University, Tokushima, Japan.
Hiroto KatohDepartment of Genomic Pathology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Reiko SatoDepartment of Genomic Pathology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Shuhei KanagakiDepartment of Biosciences and Informatics, Faculty of Science and Technology, Keio University, Yokohama, Japan.
Yasumasa OkazakiDepartment of Pathology and Biological Responses, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.
Shinya ToyokuniDepartment of Pathology and Biological Responses, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan.ORCID http://orcid.org/0000-0002-5757-1109
Etsu TashiroDepartment of Biosciences and Informatics, Faculty of Science and Technology, Keio University, Yokohama, Japan.
Shumpei IshikawaDepartment of Genomic Pathology, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.
Toyomasa KatagiriDivision of Genome Medicine, Institute for Genome Research, Tokushima University, Tokushima, Japan.
Masaya ImotoDepartment of Biosciences and Informatics, Faculty of Science and Technology, Keio University, Yokohama, Japan.ORCID http://orcid.org/0000-0002-9645-5426
Keio University · JPTokushima University · JPTokyo Medical and Dental University · JPNagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Xanthohumol (XN), a simple prenylated chalcone, can be isolated from hops and has the potential to be a cancer chemopreventive agent against several human tumor cell lines. We previously identified valosin-containing protein (VCP) as a target of XN; VCP can also play crucial roles in cancer progression and prognosis. Therefore, we investigated the molecular mechanisms governing the contribution of VCP to the antitumor activity of XN. Several human tumor cell lines were treated with XN to investigate which human tumor cell lines are sensitive to XN. Several cell lines exhibited high sensitivity to XN both in vitro and in vivo. shRNA screening and bioinformatics analysis identified that the inhibition of the adenylate cyclase (AC) pathway synergistically facilitated apoptosis induced by VCP inhibition. These results suggest that there is crosstalk between the AC pathway and VCP function, and targeting both VCP and the AC pathway is a potential chemotherapeutic strategy for a subset of tumor cells.

Indexed as

Xenograft Model Antitumor AssaysA549 CellsAdenosine TriphosphatasesAdenylyl CyclasesAnimalsApoptosisBlotting, WesternCell Cycle ProteinsCell Line, TumorCell ProliferationCyclic AMP-Dependent Protein KinasesFemaleFlavonoidsHCT116 CellsHeLa CellsHT29 CellsAdenosine TriphosphatasesAdenylyl CyclasesBIRC5 protein, humanCell Cycle ProteinsCyclic AMP-Dependent Protein KinasesFlavonoidsInhibitor of Apoptosis ProteinsIntracellular Signaling Peptides and ProteinsPropiophenonesprotein kinase modulatorSurvivinValosin Containing ProteinVCP protein, humanVcp protein, mousexanthohumolAdenylate cyclaseantitumor activityapoptosisvalosin-containing proteinxanthohumol

Identifiers

PMID28122154
PMCPMC5406609
OpenAlexW2581183830

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.