Evidence map›Paper›PMID 32492887›Full record

ArticleJournal of clinical medicine2020

Transplantation Induces Profound Changes in the Transcriptional Asset of Hematopoietic Stem Cells: Identification of Specific Signatures Using Machine Learning Techniques.

Daniela Cilloni, Jessica Petiti, Valentina Campia, Marina Podestà, Margherita Squillario, Nuria Montserrat, Alice Bertaina, Federica Sabatini, Sonia Carturan, Massimo Berger and 10 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

6 citing papers in PubMed, 5 citations in OpenAlex.

  1. Machine Learning in Stem Cell Research: From Biological Data to Clinical Translation.Computational and structural biotechnology journal · 2026
    Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. 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

20 authors at 8 institutions in 2 countries.

Daniela CilloniDepartment of Clinical and Biological Sciences, University of Turin, 10043 Turin, Italy.ORCID 0000-0001-6346-4791
Jessica PetitiDepartment of Clinical and Biological Sciences, University of Turin, 10043 Turin, Italy.ORCID 0000-0001-8640-2462
Valentina CampiaDepartment of Clinical and Biological Sciences, University of Turin, 10043 Turin, Italy.
Marina PodestàDepartment of Pediatric Hemato-Oncology and Stem Cell and Cellular Therapy Laboratory, Institute G. Gaslini, Largo G Gaslini, 16147 Genova, Italy.
Margherita SquillarioDepartment of Informatics, Bioengineering, Robotics and Systems Engineering, University of Genoa, via Dodecaneso 35, 16146 Genoa, Italy.
Nuria MontserratPluripotent Stem Cells and Activation of Endogenous Tissue Programs for Organ Regeneration (PR Lab), Institute for Bioengineering of Catalonia (IBEC) c/Baldiri Reixac 15-21, 08028 Barcelona, Spain.
Alice BertainaDepartment of Pediatric Hematology and Oncology IRCCS; Ospedale Pediatrico Bambino Gesù, Rome, University of Pavia, 27100 Pavia, Italy.
Federica SabatiniDepartment of Pediatric Hemato-Oncology and Stem Cell and Cellular Therapy Laboratory, Institute G. Gaslini, Largo G Gaslini, 16147 Genova, Italy.
Sonia CarturanDepartment of Clinical and Biological Sciences, University of Turin, 10043 Turin, Italy.
Massimo BergerPediatric Onco-Hematology, Stem Cell Transplantation and Cellular Therapy Divisions, Regina Margherita Children Hospital, 10126 Turin, Italy.
Francesco SaglioPediatric Onco-Hematology, Stem Cell Transplantation and Cellular Therapy Divisions, Regina Margherita Children Hospital, 10126 Turin, Italy.
Giuseppe BandiniAzienda Universitaria Ospedaliera di Bologna, Policlinico S. Orsola-Malpighi, 40138 Bologna, Italy.
Francesca BonifaziAzienda Universitaria Ospedaliera di Bologna, Policlinico S. Orsola-Malpighi, 40138 Bologna, Italy.
Franca FagioliPediatric Onco-Hematology, Stem Cell Transplantation and Cellular Therapy Divisions, Regina Margherita Children Hospital, 10126 Turin, Italy.
Lorenzo MorettaDepartment of Immunology, IRCCS Bambino Gesù Children's Hospital, 00165 Rome, Italy.
Giuseppe SaglioDepartment of Clinical and Biological Sciences, University of Turin, 10043 Turin, Italy.
Alessandro VerriDepartment of Informatics, Bioengineering, Robotics and Systems Engineering, University of Genoa, via Dodecaneso 35, 16146 Genoa, Italy.
Annalisa BarlaDepartment of Informatics, Bioengineering, Robotics and Systems Engineering, University of Genoa, via Dodecaneso 35, 16146 Genoa, Italy.ORCID 0000-0002-3436-035X
Franco LocatelliDepartment of Pediatric Hematology and Oncology IRCCS; Ospedale Pediatrico Bambino Gesù, Rome, University of Pavia, 27100 Pavia, Italy.
Francesco FrassoniDepartment of Clinical and Biological Sciences, University of Turin, 10043 Turin, Italy.
University of Turin · ITOspedale Regina Margherita · ITUniversity of Genoa · ITIRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · ITIstituto Giannina Gaslini · ITUniversity of Pavia · ITBambino Gesù Children's Hospital · ITBiomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine · ES

Funding

Associazione Italiana per la Ricerca sul Cancro 10100Associazione Italiana per la Ricerca sul Cancro 9962
6 · The paper itself

Abstract

During the phase of proliferation needed for hematopoietic reconstitution following transplantation, hematopoietic stem/progenitor cells (HSPC) must express genes involved in stem cell self-renewal. We investigated the expression of genes relevant for self-renewal and expansion of HSPC (operationally defined as CD34+ cells) in steady state and after transplantation. Specifically, we evaluated the expression of ninety-one genes that were analyzed by real-time PCR in CD34+ cells isolated from (i) 12 samples from umbilical cord blood (UCB); (ii) 15 samples from bone marrow healthy donors; (iii) 13 samples from bone marrow after umbilical cord blood transplant (UCBT); and (iv) 29 samples from patients after transplantation with adult hematopoietic cells. The results show that transplanted CD34+ cells from adult cells acquire an asset very different from transplanted CD34+ cells from cord blood. Multivariate machine learning analysis (MMLA) showed that four specific gene signatures can be obtained by comparing the four types of CD34+ cells. In several, but not all cases, transplanted HSPC from UCB overexpress reprogramming genes. However, these remarkable changes do not alter the commitment to hematopoietic lineage. Overall, these results reveal undisclosed aspects of transplantation biology.

Indexed as

cord bloodhematopoietic stem/progenitor cellstem cell transplantation

Identifiers

PMID32492887
PMCPMC7355574
OpenAlexW3029188302

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.