Evidence map›Paper›PMID 23920124›Full record

ArticleCancer letters2013

Guggulsterone decreases proliferation and metastatic behavior of pancreatic cancer cells by modulating JAK/STAT and Src/FAK signaling.

Muzafar A Macha, Satyanarayana Rachagani, Suprit Gupta, Priya Pai, Moorthy P Ponnusamy, Surinder K Batra, Maneesh Jain

Open access · greenAbstract read
In one paragraph

Article in Cancer letters, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
4.9field-weighted citation impact, top 5% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 87 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
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  7. Review
  8. Molecules (Basel, Switzerland) · 2022
    Article
  9. Article
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  11. Observational
  12. Article
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  16. Article
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  18. Oncostatin M receptor, positively regulated by SP1, promotes gastric cancer growth and metastasis upon treatment with Oncostatin M.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2019
    Article
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  20. 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

7 authors at 1 institution in 1 country.

Muzafar A MachaDepartment of Biochemistry and Molecular Biology, Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, Omaha, NE 68198-5870, USA.
Satyanarayana Rachagani
Suprit Gupta
Priya Pai
Moorthy P Ponnusamy
Surinder K Batra
Maneesh Jain
University of Nebraska Medical Center · US

Funding

Tissue CoreP50CA127297 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI HOLLINGSWORTH, MICHAEL A. · 2008 to 2018
$17.1M
Project 9 - Renal Drug Targeting for the Treatment of Lupus NephritisP20GM103480 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BRONICH, TATIANA K · 2012 to 2017
$13.3M
Early Diagnosis of Pancreatic CancerU01CA111294 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BATRA, SURINDER K., HOLLINGSWORTH, MICHAEL A. · 2004 to 2015
$7.1M
MOLECULAR STUDIES ON MUC4 MUCIN GENER01CA078590 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BATRA, SURINDER K. · 1998 to 2011
$2.5M
Novel deregulated genes in the etiology and progression of human prostate cancerR01CA138791 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BATRA, SURINDER K. · 2010 to 2014
$1.9M
Smoking and pancreatic cancerR01CA133774 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BATRA, SURINDER K. · 2008 to 2012
$1.8M
Molecular Markers for the Diagnosis of Pancreatic CancerR01CA131944 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BATRA, SURINDER K. · 2008 to 2012
$1.5M
Novel Combination Therapy Against Pancreatic CancerR21CA156037 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI JAIN, MANEESH · 2011 to 2012
$354k
EGFRvIII in Pancreatic CancerR03CA139285 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI JAIN, MANEESH · 2009 to 2010
$149k
Targeting MUC4 for chemosensitization of pancreatic cancerR03CA167342 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BATRA, SURINDER K. · 2012 to 2013
$143k
NCI NIH HHS P50 CA127297NCI NIH HHS R01 CA078590NCI NIH HHS R01 CA131944NCI NIH HHS R01 CA133774NCI NIH HHS R01 CA138791NCI NIH HHS R01 CA78590NCI NIH HHS R03 CA 139285NCI NIH HHS R03 CA139285NCI NIH HHS R03 CA167342NCI NIH HHS R21 CA156037NCI NIH HHS U01 CA111294NIGMS NIH HHS P20 GM103480PHS HHS U54163120
6 · The paper itself

Abstract

Inadequate efficacy, high toxicity and drug resistance associated with existing chemotherapeutic agents mandate a need for novel therapeutic strategies for highly aggressive Pancreatic Cancer (PC). Guggulsterone (GS) exhibits potent anti-proliferative effects against various cancer cells and has emerged as an attractive candidate for use in complementary or preventive cancer therapies. However, the knowledge regarding the therapeutic potential of GS in PC is still limited and needs to be explored. We studied the effect of GS on PC cell growth, motility and invasion and elucidated the molecular mechanisms associated with its anti-tumor effects. Treatment of Capan1 and CD18/HPAF PC cells with GS resulted in dose- and time-dependent growth inhibition and decreased colony formation. Further, GS treatment induced apoptosis and cell cycle arrest as assessed by Annexin-V assay and FACS analysis. Increased apoptosis following GS treatment was accompanied with Bad dephosphorylation and its translocation to the mitochondria, increased Caspase-3 activation, decreased Cyclin D1, Bcl-2 and xIAP expression. Additionally, GS treatment decreased motility and invasion of PC cells by disrupting cytoskeletal organization, inhibiting activation of FAK and Src signaling and decreased MMP9 expression. More importantly, GS treatment decreased mucin MUC4 expression in Capan1 and CD18/HPAF cells through transcriptional regulation by inhibiting Jak/STAT pathway. In conclusion, our results support the utility of GS as a potential therapeutic agent for lethal PC.

Indexed as

ApoptosisCell Cycle ProteinsCell Line, TumorCell MovementCell ProliferationCytoskeletonDose-Response Relationship, DrugFocal Adhesion Kinase 1HumansImmunoblottingIsoenzymesJanus KinasesMicroscopy, ConfocalMucin-4Neoplasm MetastasisPancreatic NeoplasmsCell Cycle ProteinsFocal Adhesion Kinase 1IsoenzymesJanus KinasesMUC4 protein, humanMucin-4pregna-4,17-diene-3,16-dionePregnenedionesPTK2 protein, humansrc-Family KinasesSTAT1 protein, humanSTAT1 Transcription FactorSTAT3 protein, humanSTAT3 Transcription FactorSTAT Transcription Factors3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromideApoptosisCell proliferationEB1EMTepithelial to mechenchymal transitionFarnesoid X receptorFXRGSGuggulesteroneGuggulsteronehead and neck squamous cell carcinomaHNSCCMotilityMTTMUC4MUC4 mucinmucin4pancreatic cancerPancreatic cancerPCsignal transduction and activator of transcriptionsiRNAsmall interfering RNASTAT

Identifiers

PMID23920124
PMCPMC3825785
OpenAlexW2102181807

What OpenQuestion holds

Textmetadata
LicenceTDM
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.