2D Cell Models & 3D Skin Models
- KSHV-infected primary lymphatic endothelial cells
- Latency-associated nuclear antigen
- KS/PEL co-culture model
- Dermal microvascular angiogenesis model
Kaposi Sarcoma (KS) is an angioproliferative malignancy caused by Human Herpesvirus-8 (HHV-8/KSHV) and is marked by vascular lesions multifocally located on the skin and in the mucosa and various organs. Protheragen provides comprehensive, one-stop preclinical drug and therapy development services tailored to address the complex challenges associated with Kaposi sarcoma.
Kaposi Sarcoma is marked by the presence of multiple tumors and is additionally linked to the human herpesvirus-8. The disease is evidenced by skin lesions and also features lymphatic and internal organ involvement. The mechanism focuses on the latency proteins of HHV-8, which includes LANA, vFLIP, and vGPCR, which triggers angiogenesis and inflammation through IL-6 in association with vascular endothelial growth factor (VEGF). There are four known subtypes: classic, endemic, iatrogenic, and epidemic or AIDS-associated. The highest rate of incidence is in the Sub-Saharan regions of Africa with an astonishing 48 cases every 1 million annually.
The disease mechanism for Kaposi Sarcoma stems from an active infection with HHV-8 that remains dormant for lifespan in endothelial cells and lymphocytes. Viral oncoproteins alter the signaling pathways of the cells, causing excessive proliferation of spindle cells and resulting in cancer. The combination of excessive inflammation and angiogenesis lead to the creation of a microenvironment that is inflammation rich, supportive to tumor growth. This tumor is able to grow due to immune suppression and the mechanisms of the body that escape immune detection. The growth of the tumor is allowed to grow uncontrolled in the skin, tissues and organs that are internal.
Therapeutic Strategy | Target / Intervention | Key Findings / Rationale | Development Stage |
Lenalidomide | CRBN (E3 ligase complex) | Clinically meaningful responses in classical KS independent of HIV status | Phase II |
Bevacizumab | VEGFA ligand (isoform-specific) | Monotherapy responses observed; extended PFS when combined with pegylated liposomal doxorubicin | Phase II |
Sorafenib | VEGFR2 (KDR), PDGFRβ, RAF1 | Disease stabilization in refractory KS | Phase II |
Pembrolizumab | PD-1 (PDCD1 protein) | Responses across KS subtypes; caution required in HIV+ patients due to IRIS risk | Phase II |
Disclaimer: Protheragen focuses on providing preclinical research services. This table is for information exchange purposes only. This table is not a treatment plan recommendation. For guidance on treatment options, please visit a regular hospital.
Protheragen delivers end-to-end preclinical support for Kaposi sarcoma, combining specialized therapeutic platforms with pathogenesis-driven disease models. Harness our virology and dermatopathology expertise to accelerate your KS drug development.
Protheragen leverages customizable in vitro platforms including 2D cell models and 3D skin models to model KS virology and angiogenesis, while our in vivo suite utilizes animal models to recapitulate disease progression. All models undergo stringent biomarker and functional validation to ensure clinical relevance for therapeutic development.
2D Cell Models & 3D Skin Models
In Vivo Pharmacokinetics Services
Protheragen provide seamless transition from initial disease modeling to drug safety evaluation and DMPK services. This unified approach delivers de-risking insights to accelerate your KS therapeutic pipeline.
Contact us to advance your Kaposi sarcoma development program.
References
All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.