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Updated: Jun 25, 2026

In Vivo Biosensor Tracks Non-apoptotic Caspase Activity in Drosophila
Published on: November 27, 2016
ING function in apoptosis in diverse model systems
Sitar Shah1, Heather Smith, Xiaolan Feng
1Southern Alberta Cancer Research Institute, Department of Biochemistry & Molecular Biology, Faculty of Medicine, University of Calgary, 3330 Hospital Dr. NW, Calgary, ABT2N4N1, Canada.
Abstract:
Genetic studies in model organisms have shown that programmed cell death (apoptosis) plays a significant role during development, where a deficiency in apoptosis results in severe and diverse diseases. Dysregulation of apoptosis also contributes to a variety of human diseases, such as cancer and autoimmune diseases. ING family proteins (ING1-ING5) are involved in many cellular processes, and appear to play a significant role in apoptosis. Loss or downregulation of ING protein function is frequently observed in different tumour types, many of which are resistant to apoptosis, thus warranting their classification as type II tumour suppressors. Several different in vitro and in vivo models have explored the role of ING proteins in regulating apoptosis. In this review, we discuss the progress that has been made in understanding ING protein function in apoptosis using in vitro studies and Mus musculus, Xenopus laevis, and Caenorhabditis elegans experimental models, with an emphasis on ING1 and ING3.
Insights
Programmed cell death (apoptosis) is crucial for development and preventing diseases like cancer. ING proteins are vital regulators of apoptosis, and their loss contributes to tumor resistance, classifying them as tumor suppressors.
Area of Science:
- Molecular Biology
- Cell Biology
- Genetics
Background:
- Programmed cell death (apoptosis) is essential for normal development and preventing diseases.
- Dysregulation of apoptosis is implicated in human conditions including cancer and autoimmune disorders.
- ING family proteins (ING1-ING5) are key regulators of cellular processes, including apoptosis.
Purpose of the Study:
- To review the role of ING proteins in regulating apoptosis.
- To highlight the significance of ING proteins as type II tumor suppressors.
- To summarize findings from in vitro and in vivo models concerning ING protein function in apoptosis.
Main Methods:
- Review of in vitro studies on ING protein function.
- Analysis of data from model organisms including Mus musculus, Xenopus laevis, and Caenorhabditis elegans.
- Focus on the roles of ING1 and ING3 proteins in apoptosis regulation.
Main Results:
- Loss or downregulation of ING proteins is common in tumors resistant to apoptosis.
- ING proteins are critical for proper apoptosis regulation during development and in disease.
- Studies in various model systems confirm the involvement of ING proteins in apoptosis.
Conclusions:
- ING proteins are critical regulators of apoptosis and function as type II tumor suppressors.
- Understanding ING protein function in apoptosis is crucial for developing new cancer therapies.
- Further research in model organisms and in vitro systems will elucidate ING protein roles in health and disease.
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Overview of Cell Death
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the 20th century...

