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Updated: Mar 16, 2026

A Fluorescence-based Protocol for Preliminary Screening of Protein Synthesis Inhibitors from Natural Sources
Published on: January 27, 2026
INGs are potential drug targets for cancer
Runyun Zhang1,2, Jianhua Jin1, Juanjuan Shi3
1Department of Oncology, Affiliated Wujin People's Hospital, Jiangsu University, Changzhou, 212017, People's Republic of China.
Purpose:
The inhibitor of growth (ING) family consists of ING1, ING2, ING3, ING4 and ING5, which function as the type II tumor suppressors. INGs regulate cell proliferation, senescence, apoptosis, differentiation, angiogenesis, DNA repair, metastasis, and invasion by multiple pathways. In addition, INGs increase cancer cell sensitivity for chemotherapy and radiotherapy, while clinical observations show that INGs are frequently lost in some types of cancers. The aim of the study was to summarize the recent progress regarding INGs regulating tumor progression.
Methods:
The literatures of INGs regulating tumor progression were searched and assayed.
Results:
The regulating signaling pathways of ING1, ING2, ING3 or ING4 on tumor progression were shown. The mechanisms of INGs on tumor suppression were also assayed.
Conclusions:
This review better summarized the signaling mechanism of INGs on tumor suppression, which provides a candidate therapy strategy for cancers.
Insights
Inhibitor of Growth (ING) proteins are crucial tumor suppressors that regulate multiple cancer pathways. This review summarizes their role in tumor progression and potential as cancer therapy strategies.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- The Inhibitor of Growth (ING) family (ING1-5) comprises type II tumor suppressors.
- ING proteins are involved in critical cellular processes including proliferation, apoptosis, senescence, and DNA repair.
- Loss of INGs is observed in various cancers, suggesting their role in tumor development.
Purpose of the Study:
- To review recent advancements in understanding how ING proteins regulate tumor progression.
- To consolidate knowledge on the signaling pathways and mechanisms by which INGs exert tumor suppressive functions.
Main Methods:
- A comprehensive literature search was conducted on studies investigating the role of INGs in tumor progression.
- Assayed and synthesized findings from relevant scientific publications.
Main Results:
- Detailed the specific signaling pathways influenced by ING1, ING2, ING3, and ING4 in tumor progression.
- Elucidated the molecular mechanisms through which INGs mediate tumor suppression.
Conclusions:
- This review synthesizes the signaling mechanisms of INGs in tumor suppression.
- Provides insights into potential therapeutic strategies targeting ING proteins for cancer treatment.
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