Evidence map›Paper›PMID 33846574›Full record

ArticleOncogene2021

Schlafen 5 as a novel therapeutic target in pancreatic ductal adenocarcinoma.

Mariafausta Fischietti, Frank Eckerdt, Gavin T Blyth, Ahmet D Arslan, William M Mati, Chidera V Oku, Ricardo E Perez, Catalina Lee-Chang, Ewa M Kosciuczuk, Diana Saleiro and 8 more

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 23 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

18 authors at 3 institutions in 3 countries.

Mariafausta FischiettiRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.ORCID http://orcid.org/0000-0002-5691-689X
Frank EckerdtRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.ORCID http://orcid.org/0000-0001-6853-850X
Gavin T BlythRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.
Ahmet D ArslanRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.
William M MatiRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.
Chidera V OkuRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.
Ricardo E PerezRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.
Catalina Lee-ChangRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.
Ewa M KosciuczukRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.
Diana SaleiroRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.
Elspeth M BeauchampRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.
Maciej S LesniakRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA.
Daniela VerzellaDepartment of Biotechnological and Applied Clinical Sciences, University of L'Aquila, L'Aquila, Italy.
Leyu SunDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Eleanor N FishToronto General Hospital Research Institute, University Health Network and Department of Immunology, University of Toronto, Toronto, ON, Canada.
Guang-Yu YangDepartment of Pathology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Wenan QiangDepartment of Obstetrics and Gynecology, Feinberg School of Medicine, Northwestern University, Evanston, IL, USA.
Leonidas C PlataniasRobert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, IL, USA. l-platanias@northwestern.edu.ORCID http://orcid.org/0000-0002-9740-7573
Northwestern University · USUniversity Health Network · CAUniversity of L'Aquila · IT

Funding

Signal Transduction of Type I Interferons in Malignant CellsR01CA077816 · NCI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PLATANIAS, LEONIDAS C. · 1998 to 2024
$6.6M
TRAINING PROGRAM IN SIGNAL TRANSDUCTION AND CANCERT32CA070085 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LEONIDAS C. PLATANIAS · 1997 to 2026
$5.7M
Targeting Novel Protein Complexes for the Treatment of Acute Myeloid LeukemiaR01CA121192 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PLATANIAS, LEONIDAS C. · 2006 to 2023
$4.1M
SLFN5: A Novel Therapeutic Target for GlioblastomaR01NS113352 · NINDS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PLATANIAS, LEONIDAS C. · 2019 to 2023
$1.7M
Signaling Pathways and Therapeutic Targeting of Leukemic CellsI01CX000916 · VA · JESSE BROWN VA MEDICAL CENTER · PI PLATANIAS, LEONIDAS C. · 2013 to 2025
–
CSRD VA I01 CX000916NCI NIH HHS R01 CA077816NCI NIH HHS R01 CA121192NCI NIH HHS T32 CA070085NINDS NIH HHS R01 NS113352
6 · The paper itself

Abstract

We provide evidence that a member of the human Schlafen (SLFN) family of proteins, SLFN5, is overexpressed in human pancreatic ductal adenocarcinoma (PDAC). Targeted deletion of SLFN5 results in decreased PDAC cell proliferation and suppresses PDAC tumorigenesis in in vivo PDAC models. Importantly, high expression levels of SLFN5 correlate with worse outcomes in PDAC patients, implicating SLFN5 in the pathophysiology of PDAC that leads to poor outcomes. Our studies establish novel regulatory effects of SLFN5 on cell cycle progression through binding/blocking of the transcriptional repressor E2F7, promoting transcription of key genes that stimulate S phase progression. Together, our studies suggest an essential role for SLFN5 in PDAC and support the potential for developing new therapeutic approaches for the treatment of pancreatic cancer through SLFN5 targeting.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsAnimalsCell Cycle ProteinsCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansMiceMolecular Targeted TherapyCell Cycle ProteinsSLFN5 protein, human

Identifiers

PMID33846574
PMCPMC8106654
OpenAlexW3155825173

What OpenQuestion holds

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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.