Evidence map›Paper›PMID 36371719›Full record

ArticleStem cells (Dayton, Ohio)2023

HSC Niche Dynamics in Regeneration, Pre-malignancy, and Cancer: Insights From Mathematical Modeling.

Rasmus Kristoffer Pedersen, Morten Andersen, Vibe Skov, Lasse Kjær, Hans C Hasselbalch, Johnny T Ottesen, Thomas Stiehl

Open access · hybridFull text read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

7 authors at 2 institutions in 2 countries.

Rasmus Kristoffer PedersenIMFUFA, Department of Science and Environment, Roskilde University, Roskilde, Denmark.ORCID 0000-0001-5946-8220
Morten AndersenIMFUFA, Department of Science and Environment, Roskilde University, Roskilde, Denmark.ORCID 0000-0001-7582-0685
Vibe SkovDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.ORCID 0000-0003-0097-7826
Lasse KjærDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.ORCID 0000-0001-6767-0226
Hans C HasselbalchDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.ORCID 0000-0003-3936-8032
Johnny T OttesenIMFUFA, Department of Science and Environment, Roskilde University, Roskilde, Denmark.ORCID 0000-0002-9786-0300
Thomas StiehlIMFUFA, Department of Science and Environment, Roskilde University, Roskilde, Denmark.ORCID 0000-0001-9686-9197
Roskilde University · DKZealand University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hematopoietic stem cell (HSC) niche is a crucial driver of regeneration and malignancy. Its interaction with hematopoietic and malignant stem cells is highly complex and direct experimental observations are challenging. We here develop a mathematical model which helps relate processes in the niche to measurable changes of stem and non-stem cell counts. HSC attached to the niche are assumed to be quiescent. After detachment HSC become activated and divide or differentiate. To maintain their stemness, the progeny originating from division must reattach to the niche. We use mouse data from literature to parametrize the model. By combining mathematical analysis and computer simulations, we systematically investigate the impact of stem cell proliferation, differentiation, niche attachment, and detachment on clinically relevant scenarios. These include bone marrow transplantation, clonal competition, and eradication of malignant cells. According to our model, sampling of blood or bulk marrow provides only limited information about cellular interactions in the niche and the clonal composition of the stem cell population. Furthermore, we investigate how interference with processes in the stem cell niche could help to increase the effect of low-dose chemotherapy or to improve the homing of genetically engineered cells.

Indexed as

Hematopoietic Stem CellsNeoplasmsAnimalsBone MarrowMiceModels, TheoreticalStem Cell Nicheclonal competitionmathematical modelingmyeloid malignanciesstem cell fitnessstem cell niche

Identifiers

PMID36371719
PMCPMC10020982
OpenAlexW4308891623

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read7
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.