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Published on: April 25, 2018
Intracellular functions of RNA-binding protein, Musashi1, in stem and cancer cells
Mahboobeh Forouzanfar1, Liana Lachinani2, Kianoush Dormiani3
1Department of Cell and Molecular Biology and Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Hezar Jerib Ave., Azadi Square, Isfahan, P.O. Code 81746, Iran.
Abstract:
RNA-binding protein, musashi1 (MSI1), is a main protein in asymmetric cell division of the sensory organ precursor cells, whereas its expression is reported to be upregulated in cancers. This protein is a critical element in proliferation of stem and cancer stem cells, which acts through Wnt and Notch signaling pathways. Moreover, MSI1 modulates malignancy and chemoresistance of lung cancer cells via activating the Akt signaling. Due to the main role of MSI1 in metastasis and cancer development, MSI1 would be an appropriate candidate for cancer therapy. Downregulation of MSI1 inhibits proliferation of cancer stem cells and reduces the growth of solid tumors in several cancers. On the other hand, MSI1 expression is regulated by microRNAs in such a way that several different tumor suppressor miRNAs negatively regulate oncogenic MSI1 and inhibit migration and tumor metastasis. The aim of this review is summarizing the role of MSI1 in stem cell proliferation and cancer promotion.
Insights
Musashi1 (MSI1) protein drives stem cell proliferation and cancer development by activating key signaling pathways. Inhibiting MSI1 shows promise for cancer therapy by reducing tumor growth and metastasis.
Area of Science:
- Molecular Biology
- Cancer Research
- Developmental Biology
Background:
- Musashi1 (MSI1) is an RNA-binding protein crucial for asymmetric cell division in sensory organ precursors.
- MSI1 expression is frequently upregulated in various cancers, correlating with stem cell proliferation and cancer progression.
Purpose of the Study:
- To review the multifaceted role of MSI1 in stem cell proliferation and cancer promotion.
- To explore MSI1's involvement in critical signaling pathways like Wnt, Notch, and Akt in cancer.
Main Methods:
- Literature review of studies investigating MSI1 function in stem cells and cancer.
- Analysis of MSI1's regulatory mechanisms, including microRNA-mediated control.
- Examination of MSI1's impact on cancer stem cell proliferation, malignancy, and chemoresistance.
Main Results:
- MSI1 is essential for stem and cancer stem cell proliferation, acting via Wnt, Notch, and Akt signaling pathways.
- MSI1 upregulation promotes cancer malignancy, chemoresistance, and tumor growth.
- Tumor suppressor microRNAs negatively regulate MSI1, inhibiting cancer cell migration and metastasis.
Conclusions:
- MSI1 is a significant driver of cancer development and metastasis, making it a potential therapeutic target.
- Targeting MSI1 offers a promising strategy to inhibit cancer stem cell proliferation and reduce tumor burden.
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