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Sam68 is a druggable vulnerability point in cancer stem cells
Amanda Mendes da Silva1, Veronika Yevdokimova1, Yannick D Benoit2,3
1Department of Cellular and Molecular Medicine, University of Ottawa, Ottawa, ON, K1H 8M5, Canada.
Cancer Metastasis Reviews
|October 4, 2023
Summary
Src associated in mitosis of 68 kDa (Sam68) is crucial for cancer stem cell self-renewal. Targeting Sam68 with novel drugs offers a promising strategy to inhibit tumor growth and development.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Sam68 (Src associated in mitosis of 68 kDa) is a multifunctional protein involved in RNA processing and signaling.
- Recent studies identify Sam68 as a target for drugs inhibiting Wnt/β-catenin transcription.
- These drugs selectively eliminate cancer stem cell (CSC) activity by engaging Sam68.
Purpose of the Study:
- To discuss the role of Sam68 in tumorigenesis and cancer stem cell maintenance.
- To review Sam68's involvement in chromatin regulation essential for CSCs.
- To explore advances in CSC-targeting drug discovery focused on Sam68.
Main Methods:
- Literature review of Sam68's functions in cancer.
- Analysis of Sam68's role in chromatin regulation within CSCs.
- Review of drug discovery efforts targeting Sam68.
Main Results:
- Sam68 plays a significant role in maintaining neoplastic self-renewal and tumor-initiating functions.
- Sam68 is implicated in chromatin regulation processes vital for CSCs.
- Modulating Sam68's cellular distribution and interactions is a key therapeutic strategy.
Conclusions:
- Sam68 is a critical vulnerability in cancer stem cells.
- Targeting Sam68 presents a promising therapeutic avenue to inhibit neoplastic stemness in human tumors.
- Further research into Sam68-targeted therapies could lead to novel cancer treatments.
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