Evidence map›Paper›PMID 31151986›Full record

ArticleBlood2019

ROR1-targeted delivery of miR-29b induces cell cycle arrest and therapeutic benefit in vivo in a CLL mouse model.

Chi-Ling Chiang, Swagata Goswami, Frank W Frissora, Zhiliang Xie, Pearlly S Yan, Ralf Bundschuh, Logan A Walker, Xiaomeng Huang, Rajeswaran Mani, Xiaokui M Mo and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 48 citations in OpenAlex.

  1. Trial
  2. Review
  3. Epigenetics in B-CLL.International journal of genomics · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Role of microRNAs in Chronic Lymphocytic Leukemia.International journal of molecular sciences · 2023
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Role of Nano-miRNAs in Diagnostics and Therapeutics.International journal of molecular sciences · 2022
    Review
  18. Review
  19. Review
  20. Article
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

17 authors at 7 institutions in 2 countries.

Chi-Ling ChiangDivision of Hematology, Department of Internal Medicine, College of Medicine.ORCID 0000-0002-0275-9673
Swagata GoswamiDivision of Hematology, Department of Internal Medicine, College of Medicine.
Frank W FrissoraDivision of Hematology, Department of Internal Medicine, College of Medicine.
Zhiliang XieDivision of Pharmaceutics, College of Pharmacy.
Pearlly S YanDivision of Hematology, Department of Internal Medicine, College of Medicine.
Ralf BundschuhDivision of Hematology, Department of Internal Medicine, College of Medicine.
Logan A WalkerComprehensive Cancer Center.ORCID 0000-0002-5378-3315
Xiaomeng HuangCenter for Affordable Nanoengineering of Polymeric Biomedical Devices.
Rajeswaran ManiDivision of Hematology, Department of Internal Medicine, College of Medicine.ORCID 0000-0002-2326-7133
Xiaokui M MoCenter for Biostatistics, The Ohio State University, Columbus, OH.
Sivasubramanian BaskarHematology Branch, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD.
Christoph RaderDepartment of Immunology and Microbiology, The Scripps Research Institute, Jupiter, FL.ORCID 0000-0001-9955-3454
Mitch A PhelpsComprehensive Cancer Center.
Guido MarcucciDepartment of Hematology, Gehr Family Center for Leukemia Research, City of Hope, Duarte, CA; and.
John C ByrdDivision of Hematology, Department of Internal Medicine, College of Medicine.
L James LeeCenter for Affordable Nanoengineering of Polymeric Biomedical Devices.
Natarajan MuthusamyDivision of Hematology, Department of Internal Medicine, College of Medicine.
Comprehensive Blood & Cancer Center · USThe Ohio State University · USAmerican Association of Colleges of Pharmacy · USCity of Hope · USNational Institutes of Health · USScripps Research Institute · USUniversity of Utah · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Daniel G. Stover · 1985 to 2026
$132.3M
TWO SIGNAL REQUIREMENT FOR NATURAL KILLER IMMUNITYP01CA095426 · NCI · OHIO STATE UNIVERSITY · PI JARJOURA, DAVID G · 2002 to 2016
$29.6M
Targeted Therapy for LeukemiaR35CA197734 · NCI · UNIVERSITY OF CINCINNATI · PI BYRD, JOHN C. · 2015 to 2021
$6.6M
Novel Enediyne-Based Antibody-Drug Conjugates for CancersR01CA204484 · NCI · UNIVERSITY OF FLORIDA · PI Natarajan Muthusamy, Ben Shen · 2017 to 2026
$4.6M
Phosphatase activation as therapeutic strategy for Chronic lymphocyic leukemiaR01CA197844 · NCI · OHIO STATE UNIVERSITY · PI MUTHUSAMY, NATARAJAN, PHELPS, MITCH A · 2015 to 2019
$2.2M
Role of Tcl1 and Par-4 in regulation of chronic lymphocytic leukemiaR01CA165469 · NCI · UNIVERSITY OF KENTUCKY · PI BONDADA, SUBBARAO, RANGNEKAR, VIVEK M · 2013 to 2017
$1.9M
Novel Immunotherapies for Lymphoid MalignanciesR01CA159296 · NCI · OHIO STATE UNIVERSITY · PI BYRD, JOHN C., MUTHUSAMY, NATARAJAN · 2012 to 2016
$1.6M
Validation of microRNAs as therapeutic targets in hematological malignanciesR01CA135332 · NCI · OHIO STATE UNIVERSITY · PI MARCUCCI, GUIDO, MUTHUSAMY, NATARAJAN · 2011 to 2015
$1.6M
Ultra-Low and Single-Cell Transcriptome Analysis in Patient-Derived Rare CLL Precursor CellsR50CA211524 · NCI · OHIO STATE UNIVERSITY · PI YAN, PEARLLY · 2016 to 2020
$745k
Protein Phosphatase PP2A and DNA damage in cell fate decisions of acute myeloid leukemic cellsF99CA245813 · NCI · OHIO STATE UNIVERSITY · PI GOSWAMI, SWAGATA · 2019 to 2020
$77k
NCI NIH HHS F99 CA245813NCI NIH HHS P01 CA095426NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA135332NCI NIH HHS R01 CA159296NCI NIH HHS R01 CA165469NCI NIH HHS R01 CA197844NCI NIH HHS R01 CA204484NCI NIH HHS R35 CA197734NCI NIH HHS R50 CA211524
6 · The paper itself

Abstract

Chronic lymphocytic leukemia (CLL) occurs in 2 major forms: aggressive and indolent. Low miR-29b expression in aggressive CLL is associated with poor prognosis. Indiscriminate miR-29b overexpression in the B-lineage of mice causes aberrance, thus warranting the need for selective introduction of miR-29b into B-CLL cells for therapeutic benefit. The oncofetal antigen receptor tyrosine kinase orphan receptor 1 (ROR1) is expressed on malignant B-CLL cells, but not normal B cells, encouraging us with ROR1-targeted delivery for therapeutic miRs. Here, we describe targeted delivery of miR-29b to ROR1

Indexed as

AnimalsBiomarkers, TumorCell Cycle CheckpointsCell Line, TumorCell SurvivalDisease Models, AnimalDNA MethylationEpigenesis, GeneticHumansImmunoconjugatesLeukemia, Lymphocytic, Chronic, B-CellMiceMicroRNAsNanoparticlesReceptor Tyrosine Kinase-like Orphan ReceptorsSurvival RateBiomarkers, TumorImmunoconjugatesMicroRNAsMIRN29a microRNA, humanReceptor Tyrosine Kinase-like Orphan ReceptorsROR1 protein, human

Identifiers

PMID31151986
PMCPMC6676131
OpenAlexW2947287113

What Socratic 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 Socratic graph.