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Updated: Sep 29, 2025

A Flow Cytometry-Based Cell Surface Protein Binding Assay for Assessing Selectivity and Specificity of an Anticancer Aptamer
Published on: September 13, 2022
Protein synthesis control in cancer: selectivity and therapeutic targeting
Joanna R Kovalski1,2, Duygu Kuzuoglu-Ozturk1,2, Davide Ruggero1,2,3
1Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA, USA.
Abstract:
Translational control of mRNAs is a point of convergence for many oncogenic signals through which cancer cells tune protein expression in tumorigenesis. Cancer cells rely on translational control to appropriately adapt to limited resources while maintaining cell growth and survival, which creates a selective therapeutic window compared to non-transformed cells. In this review, we first discuss how cancer cells modulate the translational machinery to rapidly and selectively synthesize proteins in response to internal oncogenic demands and external factors in the tumor microenvironment. We highlight the clinical potential of compounds that target different translation factors as anti-cancer therapies. Next, we detail how RNA sequence and structural elements interface with the translational machinery and RNA-binding proteins to coordinate the translation of specific pro-survival and pro-growth programs. Finally, we provide an overview of the current and emerging technologies that can be used to illuminate the mechanisms of selective translational control in cancer cells as well as within the microenvironment.
Insights
Cancer cells exploit mRNA translation for growth and survival, presenting a therapeutic target. This review explores targeting translational control for novel anti-cancer therapies.
Area of Science:
- Molecular Biology
- Cancer Biology
- Biochemistry
Background:
- Cancer cells utilize mRNA translational control to adapt to limited resources and maintain growth.
- This adaptive mechanism creates a selective therapeutic window for targeting cancer cells.
- Oncogenic signals converge on translational control, influencing protein expression during tumorigenesis.
Purpose of the Study:
- To review how cancer cells modulate translational machinery for protein synthesis.
- To highlight the clinical potential of targeting translation factors as anti-cancer therapies.
- To detail the role of RNA elements and RNA-binding proteins in coordinating translation.
Main Methods:
- Review of current literature on translational control in cancer.
- Analysis of oncogenic signaling pathways impacting translation.
- Discussion of RNA sequence and structural elements in translational regulation.
- Overview of emerging technologies for studying translational control.
Main Results:
- Cancer cells selectively synthesize proteins by modulating the translational machinery.
- RNA sequence and structural elements, along with RNA-binding proteins, coordinate pro-survival and pro-growth translation.
- Compounds targeting translation factors show clinical potential as anti-cancer agents.
Conclusions:
- Targeting mRNA translation offers a promising strategy for cancer therapy.
- Understanding selective translational control mechanisms is crucial for developing effective treatments.
- Emerging technologies will further illuminate translational regulation in the tumor microenvironment.
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