Evidence map›Paper›PMID 25389774›Full record

ArticlePloS one2014

Potent anti-cancer effect of 3'-hydroxypterostilbene in human colon xenograft tumors.

Tzu-Chun Cheng, Ching-Shu Lai, Min-Ching Chung, Nagabhushanam Kalyanam, Muhammed Majeed, Chi-Tang Ho, Yuan-Soon Ho, Min-Hsiung Pan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 47 citations in OpenAlex.

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  16. Marine steroid derived from Acropora formosa enhances mitochondrial-mediated apoptosis in non-small cell lung cancer cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
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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

8 authors at 5 institutions in 2 countries.

Tzu-Chun ChengGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Ching-Shu LaiInstitute of Food Science and Technology, National Taiwan University, Taipei, Taiwan.
Min-Ching ChungInstitute of Food Science and Technology, National Taiwan University, Taipei, Taiwan.
Nagabhushanam KalyanamSabinsa Corporation, East Windsor, New Jersey, United States of America.
Muhammed MajeedSabinsa Corporation, East Windsor, New Jersey, United States of America.
Chi-Tang HoDepartment of Food Science, Rutgers University, New Brunswick, New Jersey, United States of America.
Yuan-Soon HoGraduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan; Department of Laboratory Medicine, Taipei Medical University Hospital, Taipei, Taiwan; School of Medical Laboratory Science and Biotechnology, College of Medical Science and Technology, Taipei Medical University, Taipei, Taiwan; Comprehensive Cancer Center, Taipei Medical University, Taipei, Taiwan.
Min-Hsiung PanInstitute of Food Science and Technology, National Taiwan University, Taipei, Taiwan; Department of Medical Research, China Medical University Hospital, China Medical University, Taichung, Taiwan.
National Taiwan University · TWSabin Vaccine Institute · USTaipei Medical University · TWChina Medical University Hospital · TWRutgers, The State University of New Jersey · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here we report that 3'-hydroxypterostilbene (HPSB), a natural pterostilbene analogue, was more potent than pterostilbene against the growth of human cancer cells (COLO 205, HCT-116, and HT-29) with measured IC50 values of 9.0, 40.2, and 70.9 µM, respectively. We found that HPSB effectively inhibited the growth of human colon cancer cells by inducing apoptosis and autophagy. Autophagy occurred at an early stage and was observed through the formation of acidic vesicular organelles and microtubule-associated protein 1 light chain 3-II production. At the molecular levels, the results from western blot analysis showed that HPSB significantly down-regulated phosphatidylinositol 3-kinase (PI3K)/Akt and mitogen-activated protein kinases (MAPKs) signalings including decreased the phosphorylation of mammalian target of rapamycin (mTOR). Significant therapeutic effects were demonstrated in vivo by treating nude mice bearing COLO 205 tumor xenografts with HPSB (10 mg/kg i.p.). These inhibitory effects were accompanied by mechanistic down-regulation of the protein levels of cyclooxygenase-2 (COX-2), matrix metallopeptidase-9 (MMP-9), vascular endothelial growth factor (VEGF), and cyclin D1, as well as by the induction of apoptosis in colon tumors. Our findings suggest that HPSB could serve as a novel promising agent for colon cancer treatment.

Indexed as

AnimalsAntineoplastic AgentsApoptosisAutophagyCell Line, TumorCell ProliferationCell SurvivalColonic NeoplasmsCyclin D1Cyclooxygenase 2HumansInhibitory Concentration 50MaleMAP Kinase Signaling SystemMatrix Metalloproteinase 9Mice3'-hydroxypterostilbeneAntineoplastic AgentsCyclin D1Cyclooxygenase 2Matrix Metalloproteinase 9Phosphatidylinositol 3-KinasepterostilbeneStilbenesVascular Endothelial Growth Factor A

Identifiers

PMID25389774
PMCPMC4229093
OpenAlexW2125970611

What OpenQuestion holds

Textmetadata
LicenceCC0
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.