Evidence map›Paper›PMID 28457664›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2017

In Vivo Delivery and Therapeutic Effects of a MicroRNA on Colorectal Liver Metastases.

Go Oshima, Nining Guo, Chunbai He, Melinda E Stack, Christopher Poon, Abhineet Uppal, Sean C Wightman, Akash Parekh, Kinga B Skowron, Mitchell C Posner and 3 more

Abstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
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

25 citing papers in PubMed.

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  15. Non-coding RNAS and colorectal cancer liver metastasis.Molecular and cellular biochemistry · 2020
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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.

Go OshimaDepartment of Surgery, The University of Chicago, Chicago, IL 60637, USA.
Nining GuoDepartment of Radiation and Cellular Oncology, The University of Chicago, Chicago, IL 60637, USA; Department of Chemistry, The University of Chicago, Chicago, IL 60637, USA.
Chunbai HeDepartment of Chemistry, The University of Chicago, Chicago, IL 60637, USA.
Melinda E StackDepartment of Surgery, The University of Chicago, Chicago, IL 60637, USA.
Christopher PoonDepartment of Chemistry, The University of Chicago, Chicago, IL 60637, USA.
Abhineet UppalDepartment of Surgery, The University of Chicago, Chicago, IL 60637, USA.
Sean C WightmanDepartment of Surgery, The University of Chicago, Chicago, IL 60637, USA.
Akash ParekhDepartment of Radiation and Cellular Oncology, The University of Chicago, Chicago, IL 60637, USA.
Kinga B SkowronDepartment of Surgery, The University of Chicago, Chicago, IL 60637, USA.
Mitchell C PosnerDepartment of Surgery, The University of Chicago, Chicago, IL 60637, USA.
Wenbin LinDepartment of Chemistry, The University of Chicago, Chicago, IL 60637, USA. Electronic address: wenbinlin@uchicago.edu.
Nikolai N KhodarevDepartment of Radiation and Cellular Oncology, The University of Chicago, Chicago, IL 60637, USA; Ludwig Center for Metastasis Research, The University of Chicago, Chicago, IL 60637, USA. Electronic address: n-khodarev@uchicago.edu.
Ralph R WeichselbaumDepartment of Radiation and Cellular Oncology, The University of Chicago, Chicago, IL 60637, USA; Ludwig Center for Metastasis Research, The University of Chicago, Chicago, IL 60637, USA. Electronic address: rrw@radonc.uchicago.edu.

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI MARK W. LINGEN · 1985 to 2026
$122.1M
Nanoscale Metal-organic Frameworks for Light Triggered and X-ray Induced Photodynamic Therapy of Head and Neck CancersU01CA198989 · NCI · UNIVERSITY OF CHICAGO · PI LIN, WENBIN, WEICHSELBAUM, RALPH R · 2015 to 2019
$3.0M
NCI NIH HHS P30 CA014599NCI NIH HHS U01 CA198989
6 · The paper itself

Abstract

Multiple therapeutic agents are typically used in concert to effectively control metastatic tumors. Recently, we described microRNAs that are associated with the oligometastatic state, in which a limited number of metastatic tumors progress to more favorable outcomes. Here, we report the effective delivery of an oligometastatic microRNA (miR-655-3p) to colorectal liver metastases using nanoscale coordination polymers (NCPs). The NCPs demonstrated a targeted and prolonged distribution of microRNAs to metastatic liver tumors. Tumor-targeted microRNA miR-655-3p suppressed tumor growth when co-delivered with oxaliplatin, suggesting additive or synergistic interactions between microRNAs and platinum drugs. This is the first known example of systemically administered nanoparticles delivering an oligometastatic microRNA to advanced metastatic liver tumors and demonstrating tumor-suppressive effects. Our results suggest a potential therapeutic strategy for metastatic liver disease by the co-delivery of microRNAs and conventional cytotoxic agents using tumor-specific NCPs.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsAntineoplastic AgentsCholesterolColorectal NeoplasmsDihydroxyphenylalanineDisease Models, AnimalDrug CarriersDrug SynergismFemaleHCT116 CellsHumansLiver NeoplasmsMiceMice, NudeMicroRNAsAntineoplastic AgentsCholesterolDihydroxyphenylalanineDrug CarriersMicroRNAsMIRN655 microRNA, humanOrganoplatinum CompoundsOxaliplatinpolyethylene glycol 2000Polyethylene Glycolscolorectal cancerlivermetastasesmicroRNAnanoparticles

Identifiers

PMID28457664
PMCPMC5498809

What OpenQuestion holds

Textmetadata
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.