Evidence map›Paper›PMID 21881595›Full record

ArticleGenes and immunity2012

Systemic in vivo lentiviral delivery of miR-15a/16 reduces malignancy in the NZB de novo mouse model of chronic lymphocytic leukemia.

S Kasar, E Salerno, Y Yuan, C Underbayev, D Vollenweider, M F Laurindo, H Fernandes, D Bonci, A Addario, F Mazzella and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Genes and immunity, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

41 citing papers in PubMed, 82 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Role of microRNAs in Chronic Lymphocytic Leukemia.International journal of molecular sciences · 2023
    Review
  5. Review
  6. Review
  7. Review
  8. miRNA: A Promising Therapeutic Target in Cancer.International journal of molecular sciences · 2022
    Review
  9. Review
  10. [Application of tetrahedral framework nucleic acids in the treatment of osteoarthritis].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2022
    Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Recent Advances in miRNA Delivery Systems.Methods and protocols · 2021
    Article
  19. Review
  20. Review
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

11 authors at 3 institutions in 2 countries.

S KasarDepartment of Pathology and Lab Medicine, University of Medicine and Dentistry/New Jersey Medical School, Newark, NJ 07103, USA.
E Salerno
Y Yuan
C Underbayev
D Vollenweider
M F Laurindo
H Fernandes
D Bonci
A Addario
F Mazzella
E Raveche
Rutgers, The State University of New Jersey · USRutgers New Jersey Medical SchoolIstituto Superiore di Sanità · IT

Funding

Studies of the role of microRNA miR-16-1 in the NZB mouse model of CLLR01CA129826 · NCI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI RAVECHE, ELIZABETH S · 2010 to 2012
$938k
NCI NIH HHS R01 CA129826NCI NIH HHS R01CA129826
6 · The paper itself

Abstract

Similar to human chronic lymphocytic leukemia (CLL), the de novo New Zealand Black (NZB) mouse model has a genetically determined age-associated increase in malignant B-1 clones and decreased expression of microRNAs miR-15a and miR-16 in B-1 cells. In the present study, lentiviral vectors were employed in vivo to restore miR-15a/16, and both the short-term single injection and long-term multiple injection effects of this delivery were observed in NZB. Control lentivirus without the mir-15a/16 sequence was used for comparison. We found that in vivo lentiviral delivery of mir-15a/16 increased miR-15a/16 expression in cells that were transduced (detected by GFP expression) and in sera when compared with control lentivirus treatment. More importantly, mice treated with the miR-expressing lentivirus had decreased disease. The lentivirus had little systemic toxicity while preferentially targeting B-1 cells. Short-term effects on B-1 cells were direct effects, and only malignant B-1 cells transduced with miR-15a/16 lentivirus had decreased viability. In contrast, long-term studies suggested both direct and indirect effects resulting from miR-15a/16 lentivirus treatment. A decrease in B-1 cells was found in both the transduced and non-transduced populations. Our data support the potential use of systemic lentiviral delivery of miR-15a/16 to ameliorate disease manifestations of CLL.

Indexed as

AnimalsDisease Models, AnimalGenetic TherapyLentivirusLeukemia, Lymphocytic, Chronic, B-CellMiceMicroRNAsMicroRNAs

Identifiers

PMID21881595
PMCPMC3516396
OpenAlexW2052395000

What OpenQuestion holds

Textmetadata
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.