首页 | 官方网站   微博 | 高级检索  
     


Role of HHV‐8 and mTOR pathway in post‐transplant Kaposi sarcoma staging
Authors:Astrid Hernández‐Sierra  Jordi Rovira  Anna Petit  Daniel Moya‐Rull  María Auxiliadora Mazuecos  Ana Isabel Sánchez‐Fructuoso  Pedro Errasti  Miguel Ángel Idoate  Josep María Cruzado  August Vidal  Fritz Diekmann  Federico Oppenheimer  Josep M Campistol  Ignacio Revuelta
Affiliation:1. Department of Nephrology and Renal Transplantation, Hospital Clínic de Barcelona, Barcelona, Spain;2. Laboratori Experimental de Nefrologia i Trasplantament (LENIT), Fundació Clínic – IDIBAPS, Barcelona, Spain;3. Department of Pathology, Hospital Clínic de Barcelona, Barcelona, Spain;4. Department of Nephrology, Hospital Universitario Puerta del Mar, Cadiz, Spain;5. Department of Nephrology, Hospital Clinico San Carlos, Madrid, Spain;6. Department of Nephrology, Clínica Universitaria de Navarra, Pamplona, Spain;7. Department of Pathology, Clínica Universitaria de Navarra, Pamplona, Spain;8. Renal Transplant Unit, Hospital Universitari de Bellvitge, Barcelona, Spain;9. Department of Pathology, Hospital Universitari de Bellvitge, Barcelona, Spain
Abstract:Kaposi's sarcoma (KS) is one of the most frequent transplant related tumors. Several pathways are involved; however, the impact of the molecular phenotype associated to the tumor stage and the behavior‐depending resultant therapy is still unknown. The aim of our study was to analyze the role of HHV‐8 and mTOR pathway in tumor stages of skin KS after renal transplantation. Twelve renal transplant recipients with cutaneous KS from five transplant centers (1980–2007) under reduction of immunosuppression or conversion to mTOR inhibitor were included. The expression of HHV‐8, PTEN, TGFβ, VEGF, phospho‐mTOR, and phospho‐P70S6K in tumoral tissue was analyzed. KS lesions were classified as patch, plaque, and nodule state. HHV‐8 infection was found in all tissue samples. KS lesions showed high activation of VEGF, p‐mTOR and p‐P70S6K, low PTEN, and null TGFβ expression. The only pathway activated in a staging‐dependent manner was mTOR with higher p‐mTOR and p‐P70S6K expression in nodule versus patch stage. KS lesions disappeared after 5.24 months in all converted patients without any recurrence in 14.05 years of mean follow‐up. The activation of mTOR pathway according to KS stages supports the rational of the mTOR inhibitor in post‐transplant Kaposi.
Keywords:post‐transplant malignancy  rapamycin
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司    京ICP备09084417号-23

京公网安备 11010802026262号