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Molecularly targeted therapies for nonmelanoma skin cancers
Lucinda S Liu1, Oscar R Colegio
1Department of Dermatology, Yale School of Medicine, New Haven, CT 06520-8059, USA.
Abstract:
Over the past two decades, advances in the fields of cancer genetics and molecular biology have elucidated molecular pathways that cause numerous cutaneous malignancies. This in turn has spurred the rational design of molecularly targeted therapies. In this review, we discuss the molecular pathways critical to the development of nonmelanoma skin cancers and the novel pharmacologic agents that target them. Included is a review of vismodegib for basal cell carcinoma, cetuximab for squamous cell carcinomas, imatinib for dermatofibrosarcoma protuberans, and sirolimus for Kaposi's sarcoma.
Insights
Advances in cancer genetics have identified molecular targets for novel therapies against skin cancers. This review covers targeted treatments for nonmelanoma skin cancers like basal cell carcinoma and squamous cell carcinoma.
Area of Science:
- Oncology
- Dermatology
- Molecular Biology
Background:
- Cancer genetics and molecular biology have revealed key pathways in cutaneous malignancies.
- This understanding has enabled the development of targeted therapies for skin cancers.
Purpose of the Study:
- To review molecular pathways driving nonmelanoma skin cancers.
- To discuss novel pharmacologic agents targeting these pathways.
Main Methods:
- Literature review of molecular pathways in skin cancer development.
- Review of targeted therapies including vismodegib, cetuximab, imatinib, and sirolimus.
Main Results:
- Identification of critical molecular pathways in nonmelanoma skin cancers.
- Overview of targeted agents for basal cell carcinoma, squamous cell carcinoma, dermatofibrosarcoma protuberans, and Kaposi's sarcoma.
Conclusions:
- Molecularly targeted therapies represent a significant advancement in treating nonmelanoma skin cancers.
- Understanding specific molecular pathways allows for rational drug design and improved patient outcomes.
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