Evidence map›Paper›PMID 28053325›Full record

ArticleLeukemia2017

Effects of miRNA-15 and miRNA-16 expression replacement in chronic lymphocytic leukemia: implication for therapy.

G Cutrona, S Matis, M Colombo, C Massucco, G Baio, F Valdora, L Emionite, S Fabris, A G Recchia, M Gentile and 17 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Leukemia, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Role of microRNAs in Chronic Lymphocytic Leukemia.International journal of molecular sciences · 2023
    Review
  4. Review
  5. Observational
  6. Review
  7. Article
  8. Article
  9. Review
  10. Observational
  11. Article
  12. Heterogeneity ofFrontiers in oncology · 2020
    Review
  13. miRNAs in NK Cell-Based Immune Responses and Cancer Immunotherapy.Frontiers in cell and developmental biology · 2020
    Review
  14. Review
  15. Article
  16. MicroRNAs in Autoimmunity and Hematological Malignancies.International journal of molecular sciences · 2018
    Review
  17. Article
  18. Article
  19. 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

27 authors at 7 institutions in 1 country.

G CutronaDepartment Integrated Oncological Therapies, Molecular Pathology Unit, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.ORCID 0000-0002-3335-1101
S MatisDepartment Integrated Oncological Therapies, Molecular Pathology Unit, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
M ColomboDepartment Integrated Oncological Therapies, Molecular Pathology Unit, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
C MassuccoDepartment Integrated Oncological Therapies, Molecular Pathology Unit, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
G BaioDiagnostic Imaging and Senology, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.ORCID 0000-0002-8397-5318
F ValdoraDepartment Integrated Oncological Therapies, Molecular Pathology Unit, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
L EmioniteAnimal Facility, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
S FabrisHematology Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.
A G RecchiaHematology Unit, Department of Onco-Hematology, A.O. of Cosenza, Cosenza, Italy.
M GentileHematology Unit, Department of Onco-Hematology, A.O. of Cosenza, Cosenza, Italy.
C E NeumaierDiagnostic Imaging and Senology, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
D ReverberiDepartment Integrated Oncological Therapies, Molecular Pathology Unit, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
R MassaraDepartment Integrated Oncological Therapies, Molecular Pathology Unit, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
S BoccardoDivision of Histopathology and Cytopathology, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
L BassoDepartment of Science of Health (DISSAL), University of Genoa, Genoa, Italy.
S SalviDivision of Histopathology and Cytopathology, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
F RosaDepartment of Science of Health (DISSAL), University of Genoa, Genoa, Italy.
M CilliAnimal Facility, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
S ZupoMolecular Diagnostic Unit, Division of Histopathology and Cytopathology, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
M TruiniDivision of Histopathology and Cytopathology, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
P TassoneDepartment of Experimental and Clinical Medicine, Magna Graecia University, Salvatore Venuta University Campus, Catanzaro, Italy.
M CalabreseDiagnostic Imaging and Senology, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
M NegriniDepartment of Morphology, Surgery and Experimental Medicine, University of Ferrara, Ferrara, Italy.
A NeriHematology Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.
F MorabitoHematology Unit, Department of Onco-Hematology, A.O. of Cosenza, Cosenza, Italy.
F FaisDepartment Integrated Oncological Therapies, Molecular Pathology Unit, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.ORCID 0000-0002-6643-7083
M FerrariniScientific Direction, IRCCS-A.O.U., San Martino-IST, Genoa, Italy.
Ospedale Policlinico San Martino · ITAzienda Ospedaliera di Cosenza · ITUniversity of Genoa · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITMagna Graecia University · ITUniversity of Ferrara · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic lymphocytic leukemia (CLL) clones are characterized by loss of a critical region in 13q14.3, (del(13)(q14)) involving the microRNA (miRNA) cluster miR-15a and miR-16-1. We have investigated the effects of replacement of miR-15a and miR-16-1. CLL cells transfected with these miRNA mimics exhibited a decrease in cell viability in vitro and impaired capacity for engraftment and growth in NOD/Shi-scid,γcnull (NSG) mice. No synergistic effects were observed when the two miRNA mimics were combined. The phenomena were not restricted to CLL with the del(13)(q14) lesion. Similar effects induced by miRNA mimics were seen in cells with additional chromosomal abnormalities with the exception of certain CLL clones harboring TP53 alterations. Administration of miRNA mimics to NSG mice previously engrafted with CLL clones resulted in substantial tumor regression. CLL cell transfection with miR-15a and miR-16-1-specific inhibitors resulted in increased cell viability in vitro and in an enhanced capacity of the engrafted cells to grow in NSG mice generating larger splenic nodules. These data demonstrate that the strong control by miR-15a and miR-16-1 on CLL clonal expansion is exerted also at the level of full-blown leukemia and provide indications for a miRNA-based therapeutic strategy.

Indexed as

AnimalsCell LineCell ProliferationCell SurvivalChromosome DeletionChromosomes, Human, Pair 13HeterograftsHumansLeukemia, Lymphocytic, Chronic, B-CellMiceMicroRNAsTransfectionTumor BurdenMicroRNAsMIRN15 microRNA, humanMIRN16 microRNA, human

Identifiers

PMID28053325
OpenAlexW2568656185

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.