Evidence map›Paper›PMID 31003488›Full record

ArticleCancers2019

DIRAS3-Derived Peptide Inhibits Autophagy in Ovarian Cancer Cells by Binding to Beclin1.

Margie N Sutton, Gilbert Y Huang, Xiaowen Liang, Rajesh Sharma, Albert S Reger, Weiqun Mao, Lan Pang, Philip J Rask, Kwangkook Lee, Joshua P Gray and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 29 citations in OpenAlex.

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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

16 authors at 2 institutions in 1 country.

Margie N SuttonDepartment of Experimental Therapeutics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. MNSutton@mdanderson.org.ORCID 0000-0002-9263-9877
Gilbert Y HuangDepartment of Experimental Therapeutics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. gilbertyhuang@gmail.com.
Xiaowen LiangDepartment of Experimental Therapeutics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. XLiang3@mdanderson.org.ORCID 0000-0002-6174-2951
Rajesh SharmaDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX 77030, USA. Rajesh.Sharma@bcm.edu.
Albert S RegerDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX 77030, USA. al_reger@yahoo.com.
Weiqun MaoDepartment of Experimental Therapeutics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. WMao@mdanderson.org.
Lan PangDepartment of Experimental Therapeutics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. LPang@mdanderson.org.
Philip J RaskDepartment of Experimental Therapeutics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. pjrask@mdanderson.org.
Kwangkook LeeDepartment of Experimental Therapeutics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. KLEE74@mgh.harvard.edu.
Joshua P GrayDepartment of Cancer Systems Imaging, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. jpgray@mdanderson.org.
Amy M HurwitzDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX 77030, USA. amymhz@gmail.com.
Timothy PalzkillDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX 77030, USA. timothyp@bcm.edu.
Steven W MillwardDepartment of Cancer Systems Imaging, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. smillward@mdanderson.org.
Choel KimDepartment of Pharmacology and Chemical Biology, Baylor College of Medicine, Houston, TX 77030, USA. ckim@bcm.edu.
Zhen LuDepartment of Experimental Therapeutics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. zlu@mdanderson.org.
Robert C BastDepartment of Experimental Therapeutics, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA. rbast@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
U.T. M. D. Anderson Cancer Center SPORE in Ovarian CancerP50CA217685 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SOOD, ANIL K · 2017 to 2021
$7.9M
Supplement to CA135354 "ARHI (DIRAS3) in Autophagy and Dormancy of Ovarian Cancer"R01CA135354 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BAST, ROBERT C · 2009 to 2019
$3.5M
Targeted Molecular Imaging of Cell Death in Ovarian CancerR21CA181994 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LU, ZHEN, MILLWARD, STEVEN W · 2016 to 2017
$383k
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA217685NCI NIH HHS R01 CA135354NCI NIH HHS R21 CA181994University of Texas MD Anderson Cancer Center NCI P30 CA 16672University of Texas MD Anderson Cancer Center NCI P50 CA217685University of Texas MD Anderson Cancer Center NCI P50 CA 83639
6 · The paper itself

Abstract

Autophagy can protect cancer cells from acute starvation and enhance resistance to chemotherapy. Previously, we reported that autophagy plays a critical role in the survival of dormant, drug resistant ovarian cancer cells using human xenograft models and correlated the up-regulation of autophagy and DIRAS3 expression in clinical samples obtained during "second look" operations. DIRAS3 is an imprinted tumor suppressor gene that encodes a 26 kD GTPase with homology to RAS that inhibits cancer cell proliferation and motility. Re-expression of DIRAS3 in ovarian cancer xenografts also induces dormancy and autophagy. DIRAS3 can bind to Beclin1 forming the Autophagy Initiation Complex that triggers autophagosome formation. Both the N-terminus of DIRAS3 (residues 15-33) and the switch II region of DIRAS3 (residues 93-107) interact directly with BECN1. We have identified an autophagy-inhibiting peptide based on the switch II region of DIRAS3 linked to Tat peptide that is taken up by ovarian cancer cells, binds Beclin1 and inhibits starvation-induced DIRAS3-mediated autophagy.

Indexed as

ARHIautophagy inhibitorBeclin1DIRAS3ovarian cancerpeptide therapeutic

Identifiers

PMID31003488
PMCPMC6521623
OpenAlexW2939471375

What OpenQuestion holds

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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.