Evidence map›Paper›PMID 38928344›Full record

ReviewInternational journal of molecular sciences2024

Leukemic Stem Cells and Hematological Malignancies.

Hee-Seon Choi, Byoung Soo Kim, Sik Yoon, Sae-Ock Oh, Dongjun Lee

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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. Article
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  3. Article
  4. Article
  5. Review
  6. Article
  7. The Prognostic Value of the CD8Hematology reports · 2026
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
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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

5 authors.

Hee-Seon ChoiDepartment of Convergence Medicine, School of Medicine, Pusan National University, Yangsan 50612, Republic of Korea.ORCID 0000-0002-7667-1041
Byoung Soo KimSchool of Biomedical Convergence Engineering, Pusan National University, Yangsan 50612, Republic of Korea.ORCID 0000-0002-6693-0003
Sik YoonDepartment of Anatomy, School of Medicine, Pusan National University, Yangsan 50612, Republic of Korea.ORCID 0000-0002-6449-0761
Sae-Ock OhDepartment of Anatomy, School of Medicine, Pusan National University, Yangsan 50612, Republic of Korea.
Dongjun LeeDepartment of Convergence Medicine, School of Medicine, Pusan National University, Yangsan 50612, Republic of Korea.ORCID 0000-0001-6828-401X

Funding

Basic Science Research Program through the National Research Foundation of Korea (NRF), funded by the Ministry of Education and Ministry of Health & Welfare RS-2024-00333287Ministry of Science and ICT, Ministry of Trade, Industry and Energy, Ministry of Health & Welfare, Ministry of Food and Drug Safety HX23C1692the Basic Science Research Program through the National Research Foundation of Korea (NRF), funded by the Ministry of Education and Ministry of Health & Welfare 2022R1A5A2027161the Basic Science Research Program through the National Research Foundation of Korea (NRF), funded by the Ministry of Education and Ministry of Health & Welfare RS-2023-00223764
6 · The paper itself

Abstract

The association between leukemic stem cells (LSCs) and leukemia development has been widely established in the context of genetic alterations, epigenetic pathways, and signaling pathway regulation. Hematopoietic stem cells are at the top of the bone marrow hierarchy and can self-renew and progressively generate blood and immune cells. The microenvironment, niche cells, and complex signaling pathways that regulate them acquire genetic mutations and epigenetic alterations due to aging, a chronic inflammatory environment, stress, and cancer, resulting in hematopoietic stem cell dysregulation and the production of abnormal blood and immune cells, leading to hematological malignancies and blood cancer. Cells that acquire these mutations grow at a faster rate than other cells and induce clone expansion. Excessive growth leads to the development of blood cancers. Standard therapy targets blast cells, which proliferate rapidly; however, LSCs that can induce disease recurrence remain after treatment, leading to recurrence and poor prognosis. To overcome these limitations, researchers have focused on the characteristics and signaling systems of LSCs and therapies that target them to block LSCs. This review aims to provide a comprehensive understanding of the types of hematopoietic malignancies, the characteristics of leukemic stem cells that cause them, the mechanisms by which these cells acquire chemotherapy resistance, and the therapies targeting these mechanisms.

Indexed as

Hematologic NeoplasmsNeoplastic Stem CellsAnimalsDrug Resistance, NeoplasmEpigenesis, GeneticHematopoietic Stem CellsHumansLeukemiaMutationSignal TransductionTumor Microenvironmenthematological malignancyhematopoietic stem cellleukemialeukemic stem cell

Identifiers

PMID38928344
PMCPMC11203822

What Socratic 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 Socratic graph.