Evidence map›Paper›PMID 28076793›Full record

ArticleCell reports2017

Chloroquine-Inducible Par-4 Secretion Is Essential for Tumor Cell Apoptosis and Inhibition of Metastasis.

Ravshan Burikhanov, Nikhil Hebbar, Sunil K Noothi, Nidhi Shukla, James Sledziona, Nathália Araujo, Meghana Kudrimoti, Qing Jun Wang, David S Watt, Danny R Welch and 3 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04011410 (Phase 2 Study of Hydroxychloroquine to Increase Tumor Suppressor PAR-4 Levels in Oligometastatic Prostate Cancer), which is not on this map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.3field-weighted citation impact, top 8% 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.

NCT04011410 phase2completednot on this mapstarted 2019, after this paper: background citation

Phase 2 Study of Hydroxychloroquine to Increase Tumor Suppressor PAR-4 Levels in Oligometastatic Prostate Cancer

TypeinterventionalSponsorPatrick HensleyRan2019 to 2024Enrolled20ConditionsProstate Cancer RecurrentArmsHydroxychloroquine Sulfate 200Mg Tab
3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Cancer Cell Dormancy in the Bone Microenvironment.Current osteoporosis reports · 2025
    Review
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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

13 authors at 6 institutions in 2 countries.

Ravshan BurikhanovDepartment of Radiation Medicine, University of Kentucky, Lexington, KY 40356, USA.
Nikhil HebbarGraduate Center for Toxicology and Cancer Biology, University of Kentucky, Lexington, KY 40356, USA.
Sunil K NoothiDepartment of Microbiology, Immunology and Molecular Genetics, University of Kentucky, Lexington, KY 40356, USA.
Nidhi ShuklaGraduate Center for Toxicology and Cancer Biology, University of Kentucky, Lexington, KY 40356, USA.
James SledzionaGraduate Center for Toxicology and Cancer Biology, University of Kentucky, Lexington, KY 40356, USA.
Nathália AraujoGraduate Center for Toxicology and Cancer Biology, University of Kentucky, Lexington, KY 40356, USA.
Meghana KudrimotiDepartment of Radiation Medicine, University of Kentucky, Lexington, KY 40356, USA.
Qing Jun WangGraduate Center for Toxicology and Cancer Biology, University of Kentucky, Lexington, KY 40356, USA; Molecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40356, USA.
David S WattMolecular and Cellular Biochemistry, University of Kentucky, Lexington, KY 40356, USA; Lucille Parker Markey Cancer Center, University of Kentucky, Lexington, KY 40356, USA.
Danny R WelchDepartment of Cancer Biology, University of Kansas, Kansas City, KS 66160, USA.
Jodi MaranchieDepartment of Urology, University of Pittsburgh, Pittsburgh, PA 15232, USA.
Akihiro HaradaDepartment of Cell Biology, Osaka University, Osaka 565-0871, Japan.
Vivek M RangnekarDepartment of Radiation Medicine, University of Kentucky, Lexington, KY 40356, USA; Graduate Center for Toxicology and Cancer Biology, University of Kentucky, Lexington, KY 40356, USA; Department of Microbiology, Immunology and Molecular Genetics, University of Kentucky, Lexington, KY 40356, USA; Lucille Parker Markey Cancer Center, University of Kentucky, Lexington, KY 40356, USA. Electronic address: vmrang01@email.uky.edu.
University of Kentucky · USThe Graduate Center, CUNY · USMarkey Cancer Center · USOsaka University · JPThe University of Kansas Cancer Center · USUniversity of Pittsburgh · US

Funding

University of Kentucky Markey Cancer Center Support Grant ECIA SupplementP30CA177558 · NCI · UNIVERSITY OF KENTUCKY · PI KATHLEEN L. O'CONNOR · 2013 to 2026
$38.3M
UNDERSTANDING THE MOLECULAR BASIS OF EPIGENETIC TRANSCRIPTIONAL SILENCINGP20RR020171 · NCRR · UNIVERSITY OF KENTUCKY · PI LOUIS HERSH, LOUIS HERSH LOUIS HERSH · 2004 to 2011
$16.5M
TRAINING GRANT IN MOLECULAR MECHANISMS OF TOXICITY.T32ES007266 · NIEHS · UNIVERSITY OF KENTUCKY · PI LIU, XIAOQI, MELLON, ISABEL W · 1990 to 2020
$3.7M
Interdisciplinary Research Training in Cancer BiologyT32CA165990 · NCI · UNIVERSITY OF KENTUCKY · PI Bernard Mark Evers, KATHLEEN L. O'CONNOR · 2013 to 2026
$3.2M
Role of Tcl1 and Par-4 in regulation of chronic lymphocytic leukemiaR01CA165469 · NCI · UNIVERSITY OF KENTUCKY · PI BONDADA, SUBBARAO, RANGNEKAR, VIVEK M · 2013 to 2017
$1.9M
Suppression of Prostate Tumor Growth and Metastasis by Inhibition of VimentinR01CA187273 · NCI · UNIVERSITY OF KENTUCKY · PI RANGNEKAR, VIVEK M · 2015 to 2019
$1.7M
Regulation of Par-4 Secretion in Normal Cells for Paracrine Action in Tumor CellsR21CA179283 · NCI · UNIVERSITY OF KENTUCKY · PI RANGNEKAR, VIVEK M · 2014 to 2015
$359k
NCI NIH HHS P30 CA177558NCI NIH HHS R01 CA165469NCI NIH HHS R01 CA187273NCI NIH HHS R21 CA179283NCI NIH HHS T32 CA165990NCRR NIH HHS P20 RR020171NIEHS NIH HHS T32 ES007266
6 · The paper itself

Abstract

The induction of tumor suppressor proteins capable of cancer cell apoptosis represents an attractive option for the re-purposing of existing drugs. We report that the anti-malarial drug, chloroquine (CQ), is a robust inducer of Par-4 secretion from normal cells in mice and cancer patients in a clinical trial. CQ-inducible Par-4 secretion triggers paracrine apoptosis of cancer cells and also inhibits metastatic tumor growth. CQ induces Par-4 secretion via the classical secretory pathway that requires the activation of p53. Mechanistically, p53 directly induces Rab8b, a GTPase essential for vesicle transport of Par-4 to the plasma membrane prior to secretion. Our findings indicate that CQ induces p53- and Rab8b-dependent Par-4 secretion from normal cells for Par-4-dependent inhibition of metastatic tumor growth.

Indexed as

AnimalsApoptosisCell Line, TumorCell ProliferationChloroquineHumansMiceNeoplasm MetastasisNeoplasmsOncogene ProteinsParacrine Communicationrab GTP-Binding ProteinsReceptors, ThrombinSecretory PathwayTumor Suppressor Protein p53ChloroquineOncogene Proteinsprotease-activated receptor 4Rab8b protein, humanrab GTP-Binding ProteinsReceptors, ThrombinTumor Suppressor Protein p53apoptosischloroquinemetastasis-inhibitionp53Par-4Rab8bsecretagogues

Identifiers

PMID28076793
PMCPMC5264245
OpenAlexW2569757741

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Registered trials

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.