The Dual Role of ROS in Hematological Malignancies: Stem Cell Protection and Cancer Cell Metastasis

Stem Cell Rev Rep. 2020 Apr;16(2):262-275. doi: 10.1007/s12015-019-09949-5.

Abstract

Background and objective: Reactive oxygen species (ROS) play crucial role in hematopoiesis, regulation of differentiation, self-renewal, and the balance between quiescence and proliferation of hematopoietic stem cells (HSCs). The HSCs are a small population of undifferentiated cells that reside in the bone marrow (BM) and can undergo self-renewal by giving rise to mature cells.

Methods: Relevant literature was identified through a PubMed search (2000-2019) of English-language papers using the following terms: reactive oxygen species, hematopoietic stem cell, leukemic stem cell, leukemia and chemotherapy.

Results: HSCs are very sensitive to high levels of ROS and increased production of ROS have been attributed to HSC aging. HSC aging induced by both cell intrinsic and extrinsic factors is linked to impaired HSC self-renewal and regeneration. In addition, the elevated ROS levels might even trigger differentiation of Leukemic stem cells (LSCs) and ROS may be involved in the initiation and progression of hematological malignancies, such as leukemia.

Conclusion: Targeting genes involved in ROS in LSCs and HSCs are increasingly being used as a critical target for therapeutic interventions. Appropriate concentration of ROS may be an optimal therapeutic target for treatment of leukemia during chemotherapy, but still more studies are required to better understanding of the of ROS role in blood disorders.

Keywords: Chemotherapy; Hematopoietic stem cell; Leukemic stem cell; Reactive oxygen species.

Publication types

  • Review

MeSH terms

  • Cell Self Renewal
  • Cytoprotection*
  • Hematologic Neoplasms / drug therapy
  • Hematologic Neoplasms / genetics
  • Hematologic Neoplasms / metabolism*
  • Hematologic Neoplasms / pathology
  • Hematopoietic Stem Cells / cytology*
  • Humans
  • Neoplasm Metastasis
  • Reactive Oxygen Species / metabolism*

Substances

  • Reactive Oxygen Species