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Published on: June 6, 2025
The Potential of Vitamin D-Regulated Intracellular Signaling Pathways as Targets for Myeloid Leukemia Therapy
Elzbieta Gocek1, George P Studzinski2
1Faculty of Biotechnology, University of Wroclaw, Joliot-Curie 14a, Wroclaw 50-383, Poland. elzbieta.gocek@uni.wroc.pl.
Abstract:
The current standard regimens for the treatment of acute myeloid leukemia (AML) are curative in less than half of patients; therefore, there is a great need for innovative new approaches to this problem. One approach is to target new treatments to the pathways that are instrumental to cell growth and survival with drugs that are less harmful to normal cells than to neoplastic cells. In this review, we focus on the MAPK family of signaling pathways and those that are known to, or potentially can, interact with MAPKs, such as PI3K/AKT/FOXO and JAK/STAT. We exemplify the recent studies in this field with specific relevance to vitamin D and its derivatives, since they have featured prominently in recent scientific literature as having anti-cancer properties. Since microRNAs also are known to be regulated by activated vitamin D, this is also briefly discussed here, as are the implications of the emerging acquisition of transcriptosome data and potentiation of the biological effects of vitamin D by other compounds. While there are ongoing clinical trials of various compounds that affect signaling pathways, more studies are needed to establish the clinical utility of vitamin D in the treatment of cancer.
Insights
Innovative treatments targeting cell signaling pathways like MAPK and JAK/STAT, particularly with vitamin D derivatives, show promise for acute myeloid leukemia (AML). Further research is needed to confirm clinical utility.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Standard acute myeloid leukemia (AML) treatments have limited efficacy, necessitating novel therapeutic strategies.
- Targeting cell signaling pathways crucial for cancer cell growth and survival offers a promising avenue for developing less toxic cancer drugs.
- The MAPK, PI3K/AKT/FOXO, and JAK/STAT signaling pathways are key regulators of cell proliferation and survival in cancer.
Purpose of the Study:
- To review recent advancements in targeting cell signaling pathways for AML treatment.
- To highlight the role of vitamin D and its derivatives in modulating these pathways and their anti-cancer properties.
- To discuss the interplay of microRNAs, transcriptomics, and vitamin D in cancer therapy.
Main Methods:
- Literature review of studies focusing on MAPK, PI3K/AKT/FOXO, and JAK/STAT signaling pathways in cancer.
- Analysis of research investigating the anti-cancer effects of vitamin D and its derivatives.
- Exploration of the role of microRNAs and transcriptomic data in vitamin D's biological activity.
Main Results:
- Vitamin D and its derivatives demonstrate anti-cancer properties by influencing key signaling pathways.
- Activated vitamin D regulates microRNAs, suggesting a role in post-transcriptional gene regulation in cancer.
- Emerging transcriptomic data and combination therapies may potentiate vitamin D's anti-cancer effects.
Conclusions:
- Targeting cell signaling pathways, especially with vitamin D, represents a promising strategy for novel AML therapies.
- Further clinical studies are essential to validate the therapeutic potential of vitamin D in cancer treatment.
- The integration of microRNA and transcriptomic data may offer new insights into vitamin D's mechanisms of action.
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