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In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
MicroRNAs and Growth Factors: An Alliance Propelling Tumor Progression
Merav Kedmi1, Aldema Sas-Chen2, Yosef Yarden3
1Department of Biological Regulation, Weizmann Institute of Science, Rehovot 76100, Israel. meravk@tlvmc.gov.il.
Abstract:
Tumor progression requires cancer cell proliferation, migration, invasion, and attraction of blood and lymph vessels. These processes are tightly regulated by growth factors and their intracellular signaling pathways, which culminate in transcriptional programs. Hence, oncogenic mutations often capture growth factor signaling, and drugs able to intercept the underlying biochemical routes might retard cancer spread. Along with messenger RNAs, microRNAs play regulatory roles in growth factor signaling and in tumor progression. Because growth factors regulate abundance of certain microRNAs and the latter modulate the abundance of proteins necessary for growth factor signaling, the two classes of molecules form a dense web of interactions, which are dominated by a few recurring modules. We review specific examples of the alliance formed by growth factors and microRNAs and refer primarily to the epidermal growth factor (EGF) pathway. Clinical applications of the crosstalk between microRNAs and growth factors are described, including relevance to cancer therapy and to emergence of resistance to specific drugs.
Insights
Cancer progression involves cell growth and spread, regulated by growth factors and microRNAs. Targeting their complex interactions, like the epidermal growth factor pathway, offers new therapeutic strategies for cancer treatment and drug resistance.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Signaling
Background:
- Tumor progression relies on cell proliferation, migration, invasion, and angiogenesis, processes governed by growth factors and intracellular signaling pathways.
- Growth factors and microRNAs form intricate regulatory networks crucial for tumor development and progression.
- Oncogenic mutations frequently hijack growth factor signaling, making these pathways targets for anti-cancer drugs.
Purpose of the Study:
- To review the interplay between growth factors and microRNAs in cancer progression.
- To highlight the epidermal growth factor (EGF) pathway as a key example of this crosstalk.
- To discuss the clinical implications of microRNA-growth factor interactions in cancer therapy and drug resistance.
Main Methods:
- Literature review focusing on the molecular mechanisms of growth factor and microRNA interactions in cancer.
- Analysis of signaling pathways, particularly the epidermal growth factor (EGF) pathway.
- Examination of clinical studies related to microRNA-targeted cancer therapies and drug resistance.
Main Results:
- Growth factors and microRNAs engage in a complex regulatory network, with recurring modules dominating their interactions.
- The epidermal growth factor (EGF) pathway exemplifies the critical alliance between growth factors and microRNAs in driving tumor progression.
- Specific microRNAs modulate the abundance of proteins involved in growth factor signaling, creating feedback loops.
Conclusions:
- The intricate crosstalk between growth factors and microRNAs is central to cancer cell proliferation, migration, and invasion.
- Targeting these molecular interactions, especially within the EGF pathway, holds significant promise for developing novel cancer therapies.
- Understanding this crosstalk is essential for overcoming drug resistance and improving treatment outcomes in oncology.
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