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Updated: Aug 26, 2026

A Fluorescence-based Protocol for Preliminary Screening of Protein Synthesis Inhibitors from Natural Sources
Published on: January 27, 2026
Regulation of translation and cancer
1Memorial Sloan Kettering Cancer Center, Department of Surgery (Neurosurgery), New York, New York 10021, USA. hollande@mskcc.org
Abstract:
One of the effects of oncogenic signaling appears to be differentiated recruitment of mRNA's to ribosomes. The mRNA's so affected frequently encode proteins involved in growth regulation cell-cell interaction. These functions are critical for both cancer and development, potentially suggesting that the normal role of differential translation may be during development. It is not known whether this effect is sufficient to induce cancer from cells with an initial non-neoplastic gene expression profile.
Insights
Oncogenic signaling alters messenger RNA (mRNA) translation, affecting proteins crucial for cell growth and interaction. This process, vital in development, may also drive cancer progression from normal cells.
Area of Science:
- Molecular Biology
- Oncology
- Developmental Biology
Background:
- Oncogenic signaling influences gene expression by altering messenger RNA (mRNA) recruitment to ribosomes.
- Affected mRNAs frequently encode proteins regulating cell growth and cell-cell interactions.
Purpose of the Study:
- To investigate the role of differential mRNA translation in oncogenesis.
- To explore the potential sufficiency of altered translation in inducing cancer.
Main Methods:
- Analysis of mRNA recruitment patterns to ribosomes under oncogenic signaling.
- Identification of encoded proteins and their functions.
Main Results:
- Oncogenic signaling leads to selective mRNA translation.
- The affected proteins are involved in critical growth and cell interaction pathways.
- This translational regulation mirrors processes observed in normal development.
Conclusions:
- Differential mRNA translation is a key effect of oncogenic signaling.
- The findings suggest a potential role for developmental translational mechanisms in cancer initiation.
- Further research is needed to determine if this effect alone can cause cancer.
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