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The new tumor suppressor genes ING: genomic structure and status in cancer
Damien Ythier1, Delphine Larrieu, Christian Brambilla
1Molecular Bases of Lung Cancer Progression, INSERM U823, Institut Albert Bonniot, Université Joseph Fourier, Grenoble, 38706 Cedex, France.
Abstract:
The Inhibitor of Growth 1 (ING1) gene has been identified and characterized as a Type-II tumor suppressor gene (TSG). Subsequently, 4 additional members of the family were identified by homology search. ING proteins contain a nuclear localization sequence (NLS) and a plant homeo domain (PHD) finger motif in their C-terminus. These proteins are involved in numerous signaling pathways especially in 2 tumor suppressor pathways: apoptosis and senescence. In human tumors, several studies have shown that the expression of ING1 is frequently lost or downregulated. It occurs most frequently at the RNA level, and thus epigenetics mechanism could be involved. We summarize the current knowledge on ING proteins functions and their involvement in various signaling pathways. We also review the studies that have investigated the ING protein status in human tumors. The interest of ING proteins as biomarkers and their role in tumor initiation and progression is discussed.
Insights
The Inhibitor of Growth 1 (ING1) gene, a tumor suppressor, is often lost in human cancers, suggesting epigenetic involvement. ING proteins regulate apoptosis and senescence, crucial in tumor suppression.
Area of Science:
- Molecular Biology
- Genetics
- Cancer Research
Background:
- The Inhibitor of Growth 1 (ING1) gene is a Type-II tumor suppressor gene.
- Four additional ING gene family members have been identified.
- ING proteins possess a nuclear localization sequence and a plant homeo domain finger motif.
Purpose of the Study:
- To summarize current knowledge on ING protein functions and signaling pathways.
- To review ING protein status in human tumors.
- To discuss the role of ING proteins in tumor initiation and progression.
Main Methods:
- Homology search for ING family members.
- Review of existing literature on ING protein expression in human tumors.
- Analysis of signaling pathways involving ING proteins, including apoptosis and senescence.
Main Results:
- ING1 expression is frequently lost or downregulated in human tumors, often at the RNA level.
- Epigenetic mechanisms may be involved in the downregulation of ING1.
- ING proteins are implicated in critical tumor suppressor pathways like apoptosis and senescence.
Conclusions:
- ING proteins play a significant role in tumor suppressor pathways.
- Altered ING protein expression is a common feature in human cancers.
- ING proteins hold potential as biomarkers for cancer diagnosis and prognosis.
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