Evidence map›Paper›PMID 25590830›Full record

ArticleJournal of natural products2015

Cytotoxic activity of rearranged drimane meroterpenoids against colon cancer cells via down-regulation of β-catenin expression.

In Hyun Hwang, Joonseok Oh, Wei Zhou, Seoyoung Park, Joo-Hyun Kim, Amar G Chittiboyina, Daneel Ferreira, Gyu Yong Song, Sangtaek Oh, MinKyun Na and 1 more

Abstract read
In one paragraph

Article in Journal of natural products, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
  2. Review
  3. GenusMolecules (Basel, Switzerland) · 2022
    Review
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  7. 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

11 authors.

In Hyun Hwang†Department of Chemistry, University of Iowa, Iowa City, Iowa 52242, United States.
Joonseok Oh
Wei Zhou§College of Pharmacy, Chungnam National University, Yuseong-gu, Daejeon 305-764, Republic of Korea.
Seoyoung Park⊥Department of Bio and Fermentation Convergence Technology, Kookmin University, Seoul 136-702, Republic of Korea.
Joo-Hyun Kim⊥Department of Bio and Fermentation Convergence Technology, Kookmin University, Seoul 136-702, Republic of Korea.
Amar G Chittiboyina
Daneel Ferreira
Gyu Yong Song§College of Pharmacy, Chungnam National University, Yuseong-gu, Daejeon 305-764, Republic of Korea.
Sangtaek Oh⊥Department of Bio and Fermentation Convergence Technology, Kookmin University, Seoul 136-702, Republic of Korea.
MinKyun Na§College of Pharmacy, Chungnam National University, Yuseong-gu, Daejeon 305-764, Republic of Korea.
Mark T Hamann

Funding

Natural Product HCV Drugs from Rare Plant-Microbe InteractionsR01AT007318 · NCCIH · UNIVERSITY OF MISSISSIPPI · PI HAMANN, MARK T · 2012 to 2016
$1.6M
NCCIH NIH HHS R01 AT007318NCCIH NIH HHS R01AT007318
6 · The paper itself

Abstract

Colorectal cancer has emerged as a major cause of death in Western countries. Down-regulation of β-catenin expression has been considered a promising approach for cytotoxic drug formulation. Eight 4,9-friedodrimane-type sesquiterpenoids (1-8) were acquired using the oxidative potential of Verongula rigida on bioactive metabolites from two Smenospongia sponges. Compounds 3 and 4 contain a 2,2-dimethylbenzo[d]oxazol-6(2H)-one moiety as their substituted heterocyclic residues, which is unprecedented in such types of meroterpenoids. Gauge-invariant atomic orbital NMR chemical shift calculations were employed to investigate stereochemical details with support of the application of advanced statistics such as CP3 and DP4. Compounds 2 and 8 and the mixture of 3 and 4 suppressed β-catenin response transcription (CRT) via degrading β-catenin and exhibited cytotoxic activity on colon cancer cells, implying that their anti-CRT potential is, at least in part, one of their underlying antineoplastic mechanisms.

Indexed as

Antineoplastic Agentsbeta CateninColonic NeoplasmsDown-RegulationDrug Screening Assays, AntitumorHumansMolecular StructurePolycyclic SesquiterpenesSesquiterpenesTerpenesAntineoplastic Agentsbeta CatenindrimanePolycyclic SesquiterpenesSesquiterpenesTerpenes

Identifiers

PMID25590830
PMCPMC4380199

What OpenQuestion holds

Textmetadata
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.