Evidence map›Paper›PMID 33208342›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2021

Cobomarsen, an Oligonucleotide Inhibitor of miR-155, Slows DLBCL Tumor Cell Growth

Eleni Anastasiadou, Anita G Seto, Xuan Beatty, Melanie Hermreck, Maud-Emmanuelle Gilles, Dina Stroopinsky, Lauren C Pinter-Brown, Linda Pestano, Cinzia Marchese, David Avigan and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
5.7field-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

102 citing papers in PubMed, 146 citations in OpenAlex.

  1. Review
  2. Role of miR-155 and miR-103 in Oxidative Stress in Cardiovascular Disease: A Narrative Review.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
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  5. Are RNA Therapies a Solid Foundation or a Frontier Yet to Be Conquered?International journal of molecular sciences · 2026
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  14. Molecularly targeted therapy and immunotherapy in leukemias.Journal of hematology & oncology · 2026
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42 more citing papers are in PubMed but not listed here.

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

14 authors at 4 institutions in 2 countries.

Eleni AnastasiadouHMS Initiative for RNA Medicine, Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-0212-6734
Anita G SetomiRagen Therapeutics, Inc, Boulder, Colorado.
Xuan BeattymiRagen Therapeutics, Inc, Boulder, Colorado.
Melanie HermreckmiRagen Therapeutics, Inc, Boulder, Colorado.
Maud-Emmanuelle GillesHMS Initiative for RNA Medicine, Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Dina StroopinskyDepartment of Hematology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Lauren C Pinter-BrownDepartment of Internal Medicine, Division of Hematology/Oncology, University of California, Irvine, California.
Linda PestanomiRagen Therapeutics, Inc, Boulder, Colorado.
Cinzia MarcheseDepartment of Experimental Medicine, Sapienza University of Rome, Italy.
David AviganDepartment of Hematology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts.
Pankaj TrivediDepartment of Experimental Medicine, Sapienza University of Rome, Italy.
Diana M EscolarmiRagen Therapeutics, Inc, Boulder, Colorado.
Aimee L JacksonmiRagen Therapeutics, Inc, Boulder, Colorado.
Frank J SlackHMS Initiative for RNA Medicine, Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts. fslack@bidmc.harvard.edu.
Miragen Therapeutics (United States) · USBeth Israel Deaconess Medical Center · USSapienza University of Rome · ITUniversity of California, Irvine · US

Funding

Precision microRNA medicine in cancerR35CA232105 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SLACK, FRANK J. · 2019 to 2025
$7.2M
NCI NIH HHS R35 CA232105
6 · The paper itself

Abstract

purposemiRNA-155 is an oncogenic miRNA highly expressed in B-cell malignancies, particularly in the non-germinal center B-cell or activated B-cell subtype of diffuse large B-cell lymphoma (ABC-DLBCL), where it is considered a potential diagnostic and prognostic biomarker. Thus, miR-155 inhibition represents an important therapeutic strategy for B-cell lymphomas. In this study, we tested the efficacy and pharmacodynamic activity of an oligonucleotide inhibitor of miR-155, cobomarsen, in ABC-DLBCL cell lines and in corresponding xenograft mouse models. In addition, we assessed the therapeutic efficacy and safety of cobomarsen in a patient diagnosed with aggressive ABC-DLBCL. EXPERIMENTAL

designPreclinical studies included the delivery of cobomarsen to highly miR-155-expressing ABC-DLBCL cell lines to assess any phenotypic changes, as well as intravenous injections of cobomarsen in NSG mice carrying ABC-DLBCL xenografts, to study tumor growth and pharmacodynamics of the compound over time. To begin to test its safety and therapeutic efficacy, a patient was recruited who underwent five cycles of cobomarsen treatment.

resultsCobomarsen decreased cell proliferation and induced apoptosis in ABC-DLBCL cell lines. Intravenous administration of cobomarsen in a xenograft NSG mouse model of ABC-DLBCL reduced tumor volume, triggered apoptosis, and derepressed direct miR-155 target genes. Finally, the compound reduced and stabilized tumor growth without any toxic effects for the patient.

conclusionsOur findings support the potential therapeutic application of cobomarsen in ABC-DLBCL and other types of lymphoma with elevated miR-155 expression.

Indexed as

AnimalsApoptosisCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansLymphoma, Large B-Cell, DiffuseMiceMicroRNAsOligonucleotidesOligonucleotides, AntisenseXenograft Model Antitumor AssayscobomarsenMicroRNAsMIRN155 microRNA, humanOligonucleotidesOligonucleotides, Antisense

Identifiers

PMID33208342
PMCPMC8287597
OpenAlexW3098149335

What OpenQuestion holds

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LicenceTDM
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.