Evidence map›Paper›PMID 28256037›Full record

ArticleCancer science2017

Novel small molecule inhibiting CDCP1-PKCδ pathway reduces tumor metastasis and proliferation.

Katsuhiko Nakashima, Takamasa Uekita, Shigenobu Yano, Jun-Ichi Kikuchi, Ruri Nakanishi, Nozomi Sakamoto, Keisuke Fukumoto, Akihiro Nomoto, Keisuke Kawamoto, Takashi Shibahara 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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
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  8. Pancreatic Ductal Adenocarcinoma: The Dawn of the Era of Nuclear Medicine?International journal of molecular sciences · 2021
    Review
  9. Article
  10. Review
  11. Article
  12. Exploring the Role ofFrontiers in bioengineering and biotechnology · 2020
    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

12 authors at 6 institutions in 2 countries.

Katsuhiko NakashimaDivision of Refractory and Advanced Cancer, National Cancer Center Research Institute, Tokyo, Japan.ORCID http://orcid.org/0000-0003-2970-1049
Takamasa UekitaDepartment of Applied Chemistry, National Defense Academy, Yokosuka, Japan.
Shigenobu YanoGraduate School of Materials Science, Nara Institute of Science and Technology, Nara, Japan.
Jun-Ichi KikuchiGraduate School of Materials Science, Nara Institute of Science and Technology, Nara, Japan.
Ruri NakanishiDivision of Refractory and Advanced Cancer, National Cancer Center Research Institute, Tokyo, Japan.
Nozomi SakamotoDepartment of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Osaka, Japan.
Keisuke FukumotoDepartment of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Osaka, Japan.
Akihiro NomotoDepartment of Applied Chemistry, Graduate School of Engineering, Osaka Prefecture University, Osaka, Japan.
Keisuke KawamotoDepartment of Chemistry, Graduate School of Natural Science, Kanazawa University, Kanazawa, Japan.
Takashi ShibaharaDepartment of Chemistry, Okayama University of Science, Okayama, Japan.
Hideki YamaguchiDivision of Refractory and Advanced Cancer, National Cancer Center Research Institute, Tokyo, Japan.
Ryuichi SakaiDivision of Refractory and Advanced Cancer, National Cancer Center Research Institute, Tokyo, Japan.
National Cancer Research Institute · GBOsaka Prefecture University · JPNara Institute of Science and Technology · JPKanazawa University · JPNational Defense Academy of Japan · JPOkayama University of Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CUB domain-containing protein-1 (CDCP1) is a trans-membrane protein predominantly expressed in various cancer cells and involved in tumor progression. CDCP1 is phosphorylated at tyrosine residues in the intracellular domain by Src family kinases and recruits PKCδ to the plasma membrane through tyrosine phosphorylation-dependent association with the C2 domain of PKCδ, which in turn induces a survival signal in an anchorage-independent condition. In this study, we used our cell-free screening system to identify a small compound, glycoconjugated palladium complex (Pd-Oqn), which significantly inhibited the interaction between the C2 domain of PKCδ and phosphorylated CDCP1. Immunoprecipitation assays demonstrated that Pd-Oqn hindered the intercellular interaction of phosphorylated CDCP1 with PKCδ and also suppressed the phosphorylation of PKCδ but not that of ERK or AKT. In addition, Pd-Oqn inhibited the colony formation of gastric adenocarcinoma 44As3 cells in soft agar as well as their invasion. In mouse models, Pd-Oqn markedly reduced the peritoneal dissemination of gastric adenocarcinoma cells and the tumor growth of pancreatic cancer orthotopic xenografts. These results suggest that the novel compound Pd-Oqn reduces tumor metastasis and growth by inhibiting the association between CDCP1 and PKCδ, thus potentially representing a promising candidate among therapeutic reagents targeting protein-protein interaction.

Indexed as

A549 CellsAnimalsCell AdhesionCell LineCell Line, TumorCell MovementCell ProliferationHEK293 CellsHumansMaleMAP Kinase Signaling SystemMiceMice, Inbred BALB CMice, NudeNeoplasm MetastasisNeoplasm ProteinsNeoplasm ProteinsProtein Kinase C-deltaProto-Oncogene Proteins c-aktSmall Molecule LibrariesCDCP1chemical screeningmetastasisPKCδSrc

Identifiers

PMID28256037
PMCPMC5448658
OpenAlexW2594176311

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.