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Published on: December 26, 2016
IGF2BP3 From Physiology to Cancer: Novel Discoveries, Unsolved Issues, and Future Perspectives
Caterina Mancarella1, Katia Scotlandi1
1Laboratory of Experimental Oncology, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.
Abstract:
RNA network control is a key aspect of proper cellular homeostasis. In this context, RNA-binding proteins (RBPs) play a major role as regulators of the RNA life cycle due to their capability to bind to RNA sequences and precisely direct nuclear export, translation/degradation rates, and the intracellular localization of their target transcripts. Alterations in RBP expression or functions result in aberrant RNA translation and may drive the emergence and progression of several pathological conditions, including cancer. Among the RBPs, insulin-like growth factor 2 mRNA-binding protein 3 (IGF2BP3) is of particular interest in tumorigenesis and tumor progression. This review highlights the molecular mechanisms underlying the oncogenic functions of IGF2BP3, summarizes the therapeutic potential related to its inhibition and notes the fundamental issues that remain unanswered. To fully exploit IGF2BP3 for tumor diagnosis and therapy, it is crucial to dissect the mechanisms governing IGF2BP3 re-expression and to elucidate the complex interactions between IGF2BP3 and its target mRNAs as normal cells become tumor cells.
Insights
RNA-binding proteins (RBPs) regulate cellular homeostasis, but aberrant expression, like that of insulin-like growth factor 2 mRNA-binding protein 3 (IGF2BP3), drives cancer. Understanding IGF2BP3
Area of Science:
- Molecular Biology
- Cancer Biology
- RNA Biology
Background:
- RNA-binding proteins (RBPs) are crucial regulators of RNA metabolism and cellular homeostasis.
- Dysregulation of RBPs contributes to various pathologies, notably cancer.
- Insulin-like growth factor 2 mRNA-binding protein 3 (IGF2BP3) is implicated in tumorigenesis and cancer progression.
Purpose of the Study:
- To review the molecular mechanisms of IGF2BP3's oncogenic functions.
- To summarize the therapeutic potential of targeting IGF2BP3.
- To identify unanswered questions critical for IGF2BP3-based diagnostics and therapeutics.
Main Methods:
- Literature review focusing on molecular mechanisms.
- Analysis of studies on IGF2BP3's role in cancer.
- Synthesis of current knowledge on IGF2BP3's interactions and regulation.
Main Results:
- IGF2BP3 exhibits significant oncogenic functions in tumorigenesis and progression.
- Inhibition of IGF2BP3 shows therapeutic promise for cancer treatment.
- Key unanswered questions remain regarding IGF2BP3 re-expression and target mRNA interactions.
Conclusions:
- IGF2BP3 is a critical player in cancer development and progression.
- Targeting IGF2BP3 offers a potential therapeutic strategy.
- Further research is needed to understand IGF2BP3 regulation and function in cancer.
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