Evidence map›Paper›PMID 31338813›Full record

ReviewAdvances in experimental medicine and biology2019

Signaling Pathways in Leukemic Stem Cells.

Lindsay M Gurska, Kristina Ames, Kira Gritsman

Open access · greenAbstract readReview
In one paragraph

Review in Advances in experimental medicine and biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. The Anti-Leukemic Potential of Bee Venom.International journal of general medicine · 2025
    Review
  7. Article
  8. Leukemic Stem Cells and Hematological Malignancies.International journal of molecular sciences · 2024
    Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Wnt Signaling in Leukemia and Its Bone Marrow Microenvironment.International journal of molecular sciences · 2020
    Review
  20. Targeting CXCR4 in AML and ALL.Frontiers in oncology · 2020
    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

3 authors at 1 institution in 1 country.

Lindsay M GurskaDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, New York, USA.
Kristina AmesDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, New York, USA.
Kira GritsmanDepartment of Cell Biology, Albert Einstein College of Medicine, Bronx, New York, USA. kira.gritsman@einstein.yu.edu.
Albert Einstein College of Medicine · US

Funding

TRAINING PROGRAM IN CELLULAR &MOLEC. BIOLOGY &GENETICST32GM007491 · NIGMS · YESHIVA UNIVERSITY · PI QUERY, CHARLES C · 1985 to 2021
$17.0M
Bronx-Einstein Training in Teaching and Research (BETTR), an IRACDA programK12GM102779 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Dianne Cox, Johanna Patricia Daily · 2012 to 2026
$9.2M
PI3K Isoform Dependence in Adult Hematopoiesis and Myeloid LeukemiaR01CA196973 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI GRITSMAN, KIRA · 2016 to 2020
$2.0M
Role of the Class IA PI3K in Hematopoietic Stem Cell Self-RenewalF32HL146119 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI AMES, KRISTINA · 2019 to 2022
$213k
NCI NIH HHS R01 CA196973NHLBI NIH HHS F32 HL146119NIGMS NIH HHS K12 GM102779NIGMS NIH HHS T32 GM007491
6 · The paper itself

Abstract

Hematopoietic stem cells (HSCs) and leukemic stem cells (LSCs) utilize many of the same signaling pathways for their maintenance and survival. In this review, we will focus on several signaling pathways whose roles have been extensively studied in both HSCs and LSCs. Our main focus will be on the PI3K/AKT/mTOR pathway and several of its regulators and downstream effectors. We will also discuss several other signaling pathways of particular importance in LSCs, including the WNT/β-catenin pathway, the NOTCH pathway, and the TGFβ pathway. For each of these pathways, we will emphasize differences in how these pathways operate in LSCs, compared to their function in HSCs, to highlight opportunities for the specific therapeutic targeting of LSCs. We will also highlight areas of crosstalk between multiple signaling pathways that may affect LSC function.

Indexed as

Hematopoietic Stem CellsNeoplastic Stem CellsSignal TransductionHumansOncogene Protein v-aktPhosphatidylinositol 3-KinasesTOR Serine-Threonine KinasesOncogene Protein v-aktPhosphatidylinositol 3-KinasesTOR Serine-Threonine KinasesAktFOXOHematopoietic stem cellLeukemic stem cellmTORNOTCHPI3KSignalingTGFβWNTβ-Catenin

Identifiers

PMID31338813
PMCPMC7249489
OpenAlexW2962990798

What Socratic 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 Socratic graph.