Evidence map›Paper›PMID 26983359›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2016

Targeted Delivery of C/EBPα -saRNA by Pancreatic Ductal Adenocarcinoma-specific RNA Aptamers Inhibits Tumor Growth In Vivo.

Sorah Yoon, Kai-Wen Huang, Vikash Reebye, Paul Mintz, Yu-Wen Tien, Hong-Shiee Lai, Pål Sætrom, Isabella Reccia, Piotr Swiderski, Brian Armstrong and 5 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 69 citations in OpenAlex.

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  13. Emerging Progress of RNA-Based Antitumor Therapeutics.International journal of biological sciences · 2023
    Review
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  15. Pancreatic Cancer: Nucleic Acid Drug Discovery and Targeted Therapy.Frontiers in cell and developmental biology · 2022
    Review
  16. Review
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  19. Aptamers: Cutting edge of cancer therapies.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 4 countries.

Sorah YoonDepartment of Molecular and Cellular Biology, Beckman Research Institute of City of Hope, Duarte, California, USA.
Kai-Wen HuangDepartment of Surgery and Hepatitis Research Center, National Taiwan University Hospital, College of Medicine, Taipei, Taiwan; Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan.
Vikash ReebyeDepartment of Surgery and Cancer, Imperial College London, London, UK.
Paul MintzDepartment of Surgery and Cancer, Imperial College London, London, UK.
Yu-Wen TienDepartment of Surgery and Hepatitis Research Center, National Taiwan University Hospital, College of Medicine, Taipei, Taiwan.
Hong-Shiee LaiDepartment of Surgery and Hepatitis Research Center, National Taiwan University Hospital, College of Medicine, Taipei, Taiwan.
Pål SætromDepartment of Cancer Research and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway; Department of Computer and Information Science, Norwegian University of Science and Technology, Trondheim, Norway.
Isabella RecciaDepartment of Surgery and Cancer, Imperial College London, London, UK.
Piotr SwiderskiShared Resource-DNA/RNA Peptide, Department of Molecular Medicine, Beckman Research Institute of City of Hope, Duarte, California, USA.
Brian ArmstrongLight Microscopy Core, City of Hope, Duarte, California, USA.
Agnieszka JozwiakShared Resource-DNA/RNA Peptide, Department of Molecular Medicine, Beckman Research Institute of City of Hope, Duarte, California, USA.
Duncan SpaldingDepartment of Surgery and Cancer, Imperial College London, London, UK.
Long JiaoDepartment of Surgery and Cancer, Imperial College London, London, UK.
Nagy HabibDepartment of Surgery and Cancer, Imperial College London, London, UK.
John J RossiDepartment of Molecular and Cellular Biology, Beckman Research Institute of City of Hope, Duarte, California, USA; Irell and Manella Graduate School of Biological Sciences, Beckman Research Institute of City of Hope, City of Hope, Duarte, California, USA. Electronic address: jrossi@coh.org.
Imperial College London · GBCity of Hope · USNational Taiwan University Hospital · TWBeckman Research InstituteNational Taiwan University · TWNorwegian University of Science and Technology · NO

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI XIWEI WU · 1985 to 2026
$86.3M
COMBINATORIAL USE OF CCR5 RIBOZYMES WITH ANTI HIV1 RNASR01AI042552 · NIAID · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI ROSSI, JOHN JOSEPH · 1998 to 2019
$7.8M
YEAST SYSTEM FOR DEVELOPING ANTI-HIV-1 RIBOZYMESR01AI029329 · NIAID · LOMA LINDA UNIVERSITY · PI ROSSI, JOHN JOSEPH · 1990 to 2018
$3.9M
NCI NIH HHS P30 CA033572NIAID NIH HHS R01 AI029329NIAID NIH HHS R01 AI042552
6 · The paper itself

Abstract

The 5-year survival rate for pancreatic ductal adenocarcinoma (PDAC) remains dismal despite current chemotherapeutic agents and inhibitors of molecular targets. As the incidence of PDAC constantly increases, more effective multidrug approaches must be made. Here, we report a novel method of delivering antitumorigenic therapy in PDAC by upregulating the transcriptional factor CCAAT/enhancer-binding protein-α (C/EBPα), recognized for its antiproliferative effects. Small activating RNA (saRNA) duplexes designed to increase C/EBPα expression were linked onto PDAC-specific 2'-Fluropyrimidine RNA aptamers (2'F-RNA) - P19 and P1 for construction of a cell type-specific delivery vehicle. Both P19- and P1-C/EBPα-saRNA conjugates increased expression of C/EBPα and significantly suppressed cell proliferation. Tail vein injection of the saRNA/aptamer conjugates in PANC-1 and in gemcitabine-resistant AsPC-1 mouse-xenografts led to reduced tumor size with no observed toxicity. To exploit the specificity of the P19/P1 aptamers for PDAC cells, we also assessed if conjugation with Cy3 would allow it to be used as a diagnostic tool on archival human pancreatic duodenectomy tissue sections. Scoring pattern from 72 patients suggested a positive correlation between high fluorescent signal in the high mortality patient groups. We propose a novel aptamer-based strategy for delivery of targeted molecular therapy in advanced PDAC where current modalities fail.

Indexed as

AnimalsAptamers, NucleotideCarcinoma, Pancreatic DuctalCCAAT-Enhancer-Binding Protein-alphaCell Line, TumorCell ProliferationDrug Resistance, NeoplasmHumansMiceOrgan SpecificityPancreatic NeoplasmsRNATreatment OutcomeUp-RegulationXenograft Model Antitumor AssaysAptamers, NucleotideCCAAT-Enhancer-Binding Protein-alphaRNA

Identifiers

PMID26983359
PMCPMC4923325
OpenAlexW2329472302

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.