» Articles » PMID: 35814466

Leukemic Stem Cell: A Mini-Review on Clinical Perspectives

Abstract

Hematopoietic stem cells (HSCs) are known for their ability to proliferate and self-renew, thus being responsible for sustaining the hematopoietic system and residing in the bone marrow (BM). Leukemic stem cells (LSCs) are recognized by their stemness features such as drug resistance, self-renewal, and undifferentiated state. LSCs are also present in BM, being found in only 0.1%, approximately. This makes their identification and even their differentiation difficult since, despite the mutations, they are cells that still have many similarities with HSCs. Although the common characteristics, LSCs are heterogeneous cells and have different phenotypic characteristics, genetic mutations, and metabolic alterations. This whole set of alterations enables the cell to initiate the process of carcinogenesis, in addition to conferring drug resistance and providing relapses. The study of LSCs has been evolving and its application can help patients, where through its count as a biomarker, it can indicate a prognostic factor and reveal treatment results. The selection of a target to LSC therapy is fundamental. Ideally, the target chosen should be highly expressed by LSCs, highly selective, absence of expression on other cells, in particular HSC, and preferentially expressed by high numbers of patients. In view of the large number of similarities between LSCs and HSCs, it is not surprising that current treatment approaches are limited. In this mini review we seek to describe the immunophenotypic characteristics and mechanisms of resistance presented by LSCs, also approaching possible alternatives for the treatment of patients.

Citing Articles

Anti-IL-1RAP scFv-mSA-S19-TAT fusion carrier as a multifunctional platform for versatile delivery of biotinylated payloads to myeloid leukemia cells.

Farokhi-Fard A, Rahmati S, Hashemi Aval N, Barkhordari F, Bayat E, Komijani S Sci Rep. 2024; 14(1):25080.

PMID: 39443595 PMC: 11500005. DOI: 10.1038/s41598-024-76851-7.


Recent advancements in biomarkers, therapeutics, and associated challenges in acute myeloid leukemia.

Prajapati S, Kumari N, Bhowmik D, Gupta R Ann Hematol. 2024; 103(11):4375-4400.

PMID: 39198271 DOI: 10.1007/s00277-024-05963-x.


Bone-marrow-homing lipid nanoparticles for genome editing in diseased and malignant haematopoietic stem cells.

Lian X, Chatterjee S, Sun Y, Dilliard S, Moore S, Xiao Y Nat Nanotechnol. 2024; 19(9):1409-1417.

PMID: 38783058 PMC: 11757007. DOI: 10.1038/s41565-024-01680-8.


Cancer Stem Cells from Definition to Detection and Targeted Drugs.

Ruszkowska-Ciastek B, Kwiatkowska K, Marques-da-Silva D, Lagoa R Int J Mol Sci. 2024; 25(7).

PMID: 38612718 PMC: 11011379. DOI: 10.3390/ijms25073903.


Cell Marker Accordion: interpretable single-cell and spatial omics annotation in health and disease.

Busarello E, Biancon G, Cimignolo I, Lauria F, Ibnat Z, Ramirez C bioRxiv. 2024; .

PMID: 38559181 PMC: 10979856. DOI: 10.1101/2024.03.08.584053.


References
1.
Houshmand M, Simonetti G, Circosta P, Gaidano V, Cignetti A, Martinelli G . Chronic myeloid leukemia stem cells. Leukemia. 2019; 33(7):1543-1556. PMC: 6755964. DOI: 10.1038/s41375-019-0490-0. View

2.
Sadovnik I, Hoelbl-Kovacic A, Herrmann H, Eisenwort G, Cerny-Reiterer S, Warsch W . Identification of CD25 as STAT5-Dependent Growth Regulator of Leukemic Stem Cells in Ph+ CML. Clin Cancer Res. 2015; 22(8):2051-61. PMC: 4817228. DOI: 10.1158/1078-0432.CCR-15-0767. View

3.
Corces M, Chang H, Majeti R . Preleukemic Hematopoietic Stem Cells in Human Acute Myeloid Leukemia. Front Oncol. 2017; 7:263. PMC: 5681525. DOI: 10.3389/fonc.2017.00263. View

4.
Horton S, Huntly B . Recent advances in acute myeloid leukemia stem cell biology. Haematologica. 2012; 97(7):966-74. PMC: 3396664. DOI: 10.3324/haematol.2011.054734. View

5.
Moitra K . Overcoming Multidrug Resistance in Cancer Stem Cells. Biomed Res Int. 2015; 2015:635745. PMC: 4663294. DOI: 10.1155/2015/635745. View