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Updated: Jul 19, 2026

Mapping Dysfunctional Protein-Protein Interactions in Disease
Published on: October 24, 2025
ID proteins as targets in cancer and tools in neurobiology
Antonio Iavarone1, Anna Lasorella
1Institute for Cancer Genetics, College of Physicians and Surgeons of Columbia University, New York, NY 10032, USA.
Abstract:
In eukaryotic organisms, ID proteins are key regulators of development when they function to preserve the stem cell state and prevent lineage determination. By fueling several key features of tumor progression (deregulated proliferation, invasiveness, angiogenesis and metastasis), ID proteins contribute to multiple steps of tumorigenesis. Through oncogenic processes that lead to their aberrant activation in tumors, ID proteins transfer the phenotypic traits of embryonic stem cells to cancer cells. However, ID proteins have recently emerged as highly specialized factors in post-mitotic neurons. The elevated expression of ID proteins arrests neurons in the axon growth mode and prevents cessation of axonal elongation. Here, we discuss how unique properties of ID proteins in cancer cells and neurons pave the way to unexpected therapeutic opportunities.
Insights
ID proteins regulate development and promote tumor progression by maintaining stem cell traits. In neurons, they prolong axon growth, revealing novel therapeutic avenues for cancer and neurological disorders.
Area of Science:
- Molecular Biology
- Developmental Biology
- Cancer Biology
Background:
- ID proteins are crucial regulators in eukaryotic development, maintaining stem cell pluripotency and inhibiting differentiation.
- Aberrant ID protein activity drives tumorigenesis by promoting cancer cell proliferation, invasion, angiogenesis, and metastasis.
- ID proteins confer embryonic stem cell-like properties to cancer cells through oncogenic activation.
Purpose of the Study:
- To explore the dual role of ID proteins in tumorigenesis and neuronal development.
- To discuss the unique functions of ID proteins in post-mitotic neurons, specifically in axon growth.
- To highlight potential therapeutic strategies arising from the distinct properties of ID proteins in cancer and neurons.
Main Methods:
- Review of existing literature on ID protein function in development, cancer, and neuroscience.
- Analysis of oncogenic pathways leading to aberrant ID protein activation in tumors.
- Investigation of ID protein-mediated regulation of axonal elongation in post-mitotic neurons.
Main Results:
- ID proteins are implicated in multiple stages of tumor progression, including proliferation and metastasis.
- In post-mitotic neurons, elevated ID protein levels sustain axon growth and prevent growth cessation.
- ID proteins exhibit context-dependent functions, acting as oncogenes in cancer and regulators of neuronal plasticity.
Conclusions:
- The distinct roles of ID proteins in cancer cells and neurons present unique therapeutic opportunities.
- Targeting ID proteins could offer novel strategies for treating both cancer and neurological conditions.
- Understanding ID protein regulation is key to developing innovative therapeutic interventions.
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