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An In Vitro Model for Studying Cellular Transformation by Kaposi Sarcoma Herpesvirus
Published on: August 25, 2017
Classic Kaposi's sarcoma treated with topical rapamycin
Blanca Díaz-Ley1, Emiliano Grillo, Luis Ríos-Buceta
1Department of Dermatology, Ramon y Cajal University Hospital, University of Alcalá, Madrid, Spain.
Abstract:
Kaposi's sarcoma (KS) is an angioproliferative disorder caused by human herpesvirus 8 (HHV-8). Current research efforts have focused on the study of the relative role of KSHV-encoded genes in Kaposi's sarcomagenesis in order to identify novel mechanism-based therapies for patients suffering from this tumor. Although several viral genes have potential for KS pathogenesis, compelling data point to the KSHV-encoded G protein-coupled receptor (vGPCR) as a leading candidate viral gene for the initiation of KS. Interestingly, the oncogenic potential of vGPCR seems to correlate with its capacity to activate the mammalian target of rapamycin (mTOR) signaling pathway. Rapamycin, the prototypical inhibitor of the mTOR signaling pathway, has recently emerged as an effective treatment for KS when administered orally. In this case report, we present an immunocompetent patient with KS lesions treated with topical rapamycin achieving clinical and histologic healing after 16 weeks of treatment. The topical application of rapamycin could be a novel therapeutic option for the treatment of KS.
Insights
Topical rapamycin effectively healed Kaposi's sarcoma (KS) lesions in an immunocompetent patient. This topical application of rapamycin offers a potential new treatment for KS.
Area of Science:
- Oncology
- Virology
- Dermatology
Background:
- Kaposi's sarcoma (KS) is an angioproliferative disorder linked to human herpesvirus 8 (HHV-8).
- Research focuses on HHV-8 genes, particularly viral G protein-coupled receptor (vGPCR), for KS pathogenesis.
- vGPCR's oncogenic potential is associated with activating the mammalian target of rapamycin (mTOR) pathway.
Observation:
- An immunocompetent patient with Kaposi's sarcoma lesions was treated with topical rapamycin.
- The treatment involved a 16-week course of topical rapamycin application.
Findings:
- The patient achieved complete clinical and histologic healing of KS lesions.
- Topical rapamycin demonstrated significant efficacy in treating KS.
Implications:
- Topical rapamycin represents a potential novel therapeutic strategy for Kaposi's sarcoma.
- This approach may offer a new treatment option for KS patients, particularly those seeking localized therapy.
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