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ALDH and cancer stem cells: Pathways, challenges, and future directions in targeted therapy
Kousalya Lavudi1, Shreya Madhav Nuguri2, Prashant Pandey3
1Department of Radiation Oncology, College of Medicine, The Ohio State University, Columbus, OH 43210, United States; Comprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, United States.
Abstract:
Human ALDH comprise 19 subfamilies in which ALDH1A1, ALDH1A3, ALDH3A1, ALDH5A1, ALDH7A1, and ALDH18A1 are implicated in CSC. Studies have shown that ALDH can also be involved in drug resistance and standard chemotherapy regimens are ineffective in treating patients at the stage of disease recurrence. Existing chemotherapeutic drugs eliminate the bulk of tumors but are usually not effective against CSC which express ALDH+ population. Henceforth, targeting ALDH is convincing to treat the patient's post-relapse. Combination therapies that interlink signaling mechanisms seem promising to increase the overall disease-free survival rate. Therefore, targeting ALDH through ALDH inhibitors along with immunotherapies may create a novel platform for translational research. This review aims to fill in the gap between ALDH1 family members in relation to its cell signaling mechanisms, highlighting their potential as molecular targets to sensitize recurrent tumors and bring forward the future development concerning the current progress and draw backs. This review summarizes the role of cancer stem cells and their upregulation by maintaining the tumor microenvironment in which ALDH is specifically highlighted. It discusses the regulation of ALDH family proteins and the crosstalk between ALDH and CSC in relation to cancer metabolism. Furthermore, it establishes the correlation between ALDH involved signaling mechanisms and their specific targeted inhibitors, as well as their functional modularity, bioavailability, and mechanistic role in various cancers.
Insights
Targeting aldehyde dehydrogenases (ALDH) is crucial for treating recurrent cancers, as ALDH+ cancer stem cells (CSCs) resist chemotherapy. Combination therapies involving ALDH inhibitors and immunotherapy show promise for improving survival.
Area of Science:
- Biochemistry
- Oncology
- Molecular Biology
Background:
- Aldehyde dehydrogenases (ALDH) are critical enzymes involved in various cellular processes.
- Specific ALDH subfamilies (e.g., ALDH1A1, ALDH1A3) are implicated in cancer stem cell (CSC) populations.
- ALDH expression is linked to chemoresistance and tumor recurrence, rendering standard treatments ineffective against CSCs.
Purpose of the Study:
- To review the role of ALDH family members in cancer stem cell biology and signaling mechanisms.
- To highlight ALDH as a molecular target for sensitizing recurrent tumors to therapy.
- To explore the potential of ALDH inhibitors in combination therapies for improved patient outcomes.
Main Methods:
- Literature review focusing on ALDH function, CSCs, and cancer metabolism.
- Analysis of signaling pathways regulated by ALDH family proteins.
- Examination of ALDH inhibitors, their mechanisms, and therapeutic potential.
Main Results:
- ALDH plays a key role in maintaining the tumor microenvironment and CSC populations.
- Crosstalk between ALDH and CSCs influences cancer metabolism and drug resistance.
- Targeting ALDH signaling pathways offers a strategy to overcome treatment failure in recurrent cancers.
Conclusions:
- ALDH inhibitors, particularly in combination with immunotherapy, represent a promising therapeutic strategy for recurrent cancers.
- Understanding ALDH-mediated signaling is essential for developing novel treatments that target CSCs.
- Further translational research is needed to optimize ALDH-targeted therapies for enhanced disease-free survival.
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