Evidence map›Paper›PMID 25196934›Full record

ArticleMarine drugs2014

Tricyclic guanidine alkaloids from the marine sponge Acanthella cavernosa that stabilize the tumor suppressor PDCD4.

Tanja Grkovic, Johanna S Blees, Magdalena M Bayer, Nancy H Colburn, Cheryl L Thomas, Curtis J Henrich, Megan L Peach, James B McMahon, Tobias Schmid, Kirk R Gustafson

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 15% 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, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. GenusMarine drugs · 2023
    Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Control Mechanisms of the Tumor Suppressor PDCD4: Expression and Functions.International journal of molecular sciences · 2019
    Review
  8. Review
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

10 authors at 4 institutions in 2 countries.

Tanja GrkovicMolecular Targets Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA. t.grkovic@griffith.edu.au.
Johanna S BleesMolecular Targets Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA. M_Bajer@gmx.de.
Magdalena M BayerInstitute of Biochemistry I, Faculty of Medicine, Goethe-University Frankfurt, 60590 Frankfurt, Germany. M_Bajer@gmx.de.
Nancy H ColburnLaboratory of Cancer Prevention, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA. colburna@mail.nih.gov.
Cheryl L ThomasMolecular Targets Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA. cltterry@mail.nih.gov.
Curtis J HenrichMolecular Targets Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA. henrichcj@mail.nih.gov.
Megan L PeachBasic Science Program, Leidos Biomedical Research, Inc., Chemical Biology Laboratory, Frederick National Laboratory for Cancer Research, Frederick, MD 21702, USA. mpeach@helix.nih.gov.
James B McMahonMolecular Targets Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA. mcmahoja@mail.nih.gov.
Tobias SchmidInstitute of Biochemistry I, Faculty of Medicine, Goethe-University Frankfurt, 60590 Frankfurt, Germany. M_Bajer@gmx.de.
Kirk R GustafsonMolecular Targets Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702, USA. gustafki@mail.nih.gov.
Target (United States) · USGoethe University Frankfurt · DELeidos (United States) · USNational Cancer Institute · US

Funding

Natural Products Discovery and Characterization Through Network CollaborationsZIABC011568 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI DU, LIN · 2014 to 2025
$17.2M
CCR NIH HHS HHSN261200800001CIntramural NIH HHSNCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

A cell-based high-throughput screen that assessed the cellular stability of a tumor suppressor protein PDCD4 (Programmed cell death 4) was used to identify a new guanidine-containing marine alkaloid mirabilin K (3), as well as the known compounds mirabilin G (1) and netamine M (2). The structures of these tricyclic guanidine alkaloids were established from extensive spectroscopic analyses. Compounds 1 and 2 inhibited cellular degradation of PDCD4 with EC50 values of 1.8 μg/mL and 2.8 μg/mL, respectively. Mirabilin G (1) and netamine M (2) are the first marine natural products reported to stabilize PDCD4 under tumor promoting conditions.

Indexed as

AlkaloidsAnimalsApoptosis Regulatory ProteinsGuanidineHEK293 CellsHumansOleanolic AcidPoriferaRNA-Binding ProteinsSaponinsTumor Suppressor ProteinsAlkaloidsApoptosis Regulatory ProteinsGuanidinemirabilinOleanolic AcidPDCD4 protein, humanRNA-Binding ProteinsSaponinsTumor Suppressor Proteins

Identifiers

PMID25196934
PMCPMC4145332
OpenAlexW2075067705

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.