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Exploring the impact of hydrogen sulfide on hematologic malignancies: A review.

Authors :
Lou S
Jiang ZL
Zhu YW
Zhang RY
Wang Y
Chu T
Liu YF
Zhang YX
Zhang CH
Su YK
Liu HX
Ji XY
Wu DD
Source :
Cellular signalling [Cell Signal] 2024 Aug; Vol. 120, pp. 111236. Date of Electronic Publication: 2024 May 27.
Publication Year :
2024

Abstract

Hydrogen sulfide (H <subscript>2</subscript> S) is one of the three most crucial gaseous messengers in the body. The discovery of H <subscript>2</subscript> S donors, coupled with its endogenous synthesis capability, has sparked hope for the treatment of hematologic malignancies. In the last decade, the investigation into the impact of H <subscript>2</subscript> S has expanded, particularly within the fields of cardiovascular function, inflammation, infection, and neuromodulation. Hematologic malignancies refer to a diverse group of cancers originating from abnormal proliferation and differentiation of blood-forming cells, including leukemia, lymphoma, and myeloma. In this review, we delve deeply into the complex interrelation between H <subscript>2</subscript> S and hematologic malignancies. In addition, we comprehensively elucidate the intricate molecular mechanisms by which both H <subscript>2</subscript> S and its donors intricately modulate the progression of tumor growth. Furthermore, we systematically examine their impact on pivotal aspects, encompassing the proliferation, invasion, and migration capacities of hematologic malignancies. Therefore, this review may contribute novel insights to our understanding of the prospective therapeutic significance of H <subscript>2</subscript> S and its donors within the realm of hematologic malignancies.<br />Competing Interests: Declaration of competing interest The authors declare that they have no competing interests.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-3913
Volume :
120
Database :
MEDLINE
Journal :
Cellular signalling
Publication Type :
Academic Journal
Accession number :
38810860
Full Text :
https://doi.org/10.1016/j.cellsig.2024.111236