Oncogenic human herpesvirus hijacks proline metabolism for tumorigenesis

Menée in vitro et à l'aide d'un modèle murin, cette étude met en évidence un mécanisme par lequel le virus de l'herpès associé au sarcome de Kaposi favorise la tumorigenèse en augmentant la biosynthèse de la proline

Résumé en anglais

While understanding metabolic change of tumor cells is crucial to improve cancer therapy, current 2D cell culture condition may not fully recapitulate in vivo metabolic environment of tumors. Our metabolomics analysis demonstrates that proline metabolism is critical for the KSHV-transformed cell growth in 3D culture, not in 2D culture. Specifically, the KSHV K1 oncoprotein activates PYCR proline biosynthesis enzyme, increasing intracellular proline concentration for tumor cell growth in in vitro 3D spheroid culture and in vivo tumorigenesis. This study describes an oncogenic strategy of KSHV to enhance proline synthesis for virus-induced transformation, adding the proline metabolic pathway as a potential target for KS treatment.Three-dimensional (3D) cell culture is well documented to regain intrinsic metabolic properties and to better mimic the in vivo situation than two-dimensional (2D) cell culture. Particularly, proline metabolism is critical for tumorigenesis since pyrroline-5-carboxylate (P5C) reductase (PYCR/P5CR) is highly expressed in various tumors and its enzymatic activity is essential for in vitro 3D tumor cell growth and in vivo tumorigenesis. PYCR converts the P5C intermediate to proline as a biosynthesis pathway, whereas proline dehydrogenase (PRODH) breaks down proline to P5C as a degradation pathway. Intriguingly, expressions of proline biosynthesis PYCR gene and proline degradation PRODH gene are up-regulated directly by c-Myc oncoprotein and p53 tumor suppressor, respectively, suggesting that the proline-P5C metabolic axis is a key checkpoint for tumor cell growth. Here, we report a metabolic reprogramming of 3D tumor cell growth by oncogenic Kaposi’s sarcoma-associated herpesvirus (KSHV), an etiological agent of Kaposi’s sarcoma and primary effusion lymphoma. Metabolomic analyses revealed that KSHV infection increased nonessential amino acid metabolites, specifically proline, in 3D culture, not in 2D culture. Strikingly, the KSHV K1 oncoprotein interacted with and activated PYCR enzyme, increasing intracellular proline concentration. Consequently, the K1-PYCR interaction promoted tumor cell growth in 3D spheroid culture and tumorigenesis in nude mice. In contrast, depletion of PYCR expression markedly abrogated K1-induced tumor cell growth in 3D culture, not in 2D culture. This study demonstrates that an increase of proline biosynthesis induced by K1-PYCR interaction is critical for KSHV-mediated transformation in in vitro 3D culture condition and in vivo tumorigenesis.