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Insulin-like growth factor receptor type I as a target for cancer therapy
Nathalie Corvaia1, Alain Beck, Véronique Caussanel
1Centre d'Immunologie Pierre Fabre, Saint Julien-en-Genevois, France. nathalie.corvaia@pierre-fabre.com
Abstract:
After more than 20 years of extensive work, insulin-like growth factor receptor 1 (IGF-IR) is still an attractive target for drug development. Due to its close homology to insulin receptor, IGF-IR is of interest for antibody design while antibody great specificity allows to discriminate between the two receptors. Major efforts from a large number of pharmaceutical companies are invested to evaluate the efficacy of such molecules in human without so far an obvious success. Discovery of biomarkers associated with efficacy and patient selection is one of the main challenges that we will have to deal with in order to target the appropriate patient population that will most benefit anti-IGF-IR monoclonal antibody (Mab) and combined treatments. This review will provide an overview of the current knowledge on IGF-IR axis for development of novel therapeutics in Oncology.
Insights
Insulin-like growth factor receptor 1 (IGF-IR) is a key target for cancer therapeutics. Developing effective anti-IGF-IR monoclonal antibodies (Mabs) requires identifying biomarkers for patient selection and treatment efficacy.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Insulin-like Growth Factor Receptor 1 (IGF-IR) is a validated target for cancer therapy.
- Antibodies targeting IGF-IR offer specificity due to homology with the insulin receptor.
- Despite extensive research, clinical success of anti-IGF-IR therapies remains limited.
Purpose of the Study:
- To review current knowledge of the IGF-IR axis in oncology.
- To highlight challenges and strategies for developing anti-IGF-IR monoclonal antibodies (Mabs).
- To emphasize the need for biomarkers in patient selection for targeted therapies.
Main Methods:
- Literature review of preclinical and clinical studies on IGF-IR.
- Analysis of antibody development strategies for IGF-IR.
- Discussion of biomarker discovery for patient stratification.
Main Results:
- IGF-IR remains a promising target for novel cancer therapeutics.
- Antibody-based therapies targeting IGF-IR have shown potential but face challenges in clinical efficacy.
- Biomarker identification is crucial for selecting patients likely to respond to anti-IGF-IR Mabs and combination treatments.
Conclusions:
- Further research into IGF-IR signaling is essential for advancing oncology drug development.
- Development of effective anti-IGF-IR Mabs requires robust biomarker strategies.
- Targeting the IGF-IR axis holds promise for improving outcomes in specific cancer patient populations.
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