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Published on: March 29, 2024
Insulin-like growth factor family and prostate cancer: new insights and emerging opportunities
Noha M Elemam1,2, Hassan Youssef Hotait3, Mohamed A Saleh1,2,4
1Clinical Sciences Department, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Abstract:
Prostate cancer is the second most commonly diagnosed cancer in men. The mammalian insulin-like growth factor (IGF) family is made up of three ligands (IGF-I, IGF-II, and insulin), three receptors (IGF-I receptor (IGF-1R), insulin receptor (IR), and IGF-II receptor (IGF-2R)), and six IGF-binding proteins (IGFBPs). IGF-I and IGF-II were identified as potent mitogens and were previously associated with an increased risk of cancer development including prostate cancer. Several reports showed controversy about the expression of the IGF family and their connection to prostate cancer risk due to the high degree of heterogeneity among prostate tumors, sampling bias, and evaluation techniques. Despite that, it is clear that several IGF family members play a role in prostate cancer development, metastasis, and androgen-independent progression. In this review, we aim to expand our understanding of prostate tumorigenesis and regulation through the IGF system. Further understanding of the role of IGF signaling in PCa shows promise and needs to be considered in the context of a comprehensive treatment strategy.
Insights
The insulin-like growth factor (IGF) system impacts prostate cancer (PCa) development and progression. Understanding IGF signaling is crucial for developing effective PCa treatment strategies.
Area of Science:
- Oncology
- Endocrinology
- Molecular Biology
Background:
- Prostate cancer (PCa) is a significant global health concern.
- The insulin-like growth factor (IGF) family, including ligands, receptors, and binding proteins, is implicated in cancer development.
- Previous studies show conflicting results regarding IGF family expression and PCa risk due to tumor heterogeneity and methodological variations.
Purpose of the Study:
- To review and synthesize current knowledge on the role of the IGF system in prostate tumorigenesis.
- To elucidate the regulatory mechanisms of IGF signaling in PCa.
- To highlight the potential of targeting IGF signaling in PCa treatment strategies.
Main Methods:
- Literature review of studies investigating the IGF family and prostate cancer.
- Analysis of existing data on IGF family member expression in prostate tumors.
- Synthesis of findings on the functional roles of IGF signaling in PCa progression and metastasis.
Main Results:
- IGF-I and IGF-II are potent mitogens linked to increased cancer risk, including PCa.
- Despite controversies, several IGF family members demonstrably influence PCa development, metastasis, and androgen-independent progression.
- The IGF system plays a multifaceted role in regulating prostate cancer cell growth and survival.
Conclusions:
- The IGF system is a key regulator in prostate cancer development and progression.
- Further research into IGF signaling pathways is essential for understanding PCa pathogenesis.
- Targeting the IGF system holds promise as a component of comprehensive PCa treatment strategies.
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