: Birt-Hogg-Dubé (BHD) syndrome is an inherited familial cancer syndrome characterized by the development of cutaneous lesions, pulmonary cysts, renal tumors and cysts and caused by loss-of-function pathogenic variants in the gene encoding the tumor-suppressor protein folliculin (FLCN). FLCN acts as a negative regulator of TFEB and TFE3 transcription factors, master controllers of lysosomal biogenesis and autophagy, by enabling their phosphorylation by the mechanistic Target Of Rapamycin Complex 1 (mTORC1). We have previously shown that deletion of Tfeb rescued the renal cystic phenotype of kidney-specific Flcn KO mice. Using Flcn/Tfeb/Tfe3 double and triple KO mice, we now show that both Tfeb and Tfe3 contribute, in a differential and cooperative manner, to kidney cystogenesis. Remarkably, the analysis of BHD patient-derived tumor samples revealed increased activation of TFEB/TFE3-mediated transcriptional program and silencing either of the two genes rescued tumorigenesis in human BHD renal tumor cell line-derived xenografts (CDXs). Our findings demonstrate in disease-relevant models that both TFEB and TFE3 are key drivers of renal tumorigenesis and suggest novel therapeutic strategies based on the inhibition of these transcription factors.

TFEB and TFE3 drive kidney cystogenesis and tumorigenesis / Di Malta, Chiara; Zampelli, Angela; Granieri, Letizia; Vilardo, Claudia; De Cegli, Rossella; Cinque, Laura; Nusco, Edoardo; Pece, Salvatore; Tosoni, Daniela; Sanguedolce, Francesca; Sorrentino, Nicolina Cristina; Merino, Maria J; Nielsen, Deborah; Srinivasan, Ramaprasad; Ball, Mark W; Ricketts, Christopher J; Vocke, Cathy D; Lang, Martin; Karim, Baktiar; Lanfrancone, Luisa; Schmidt, Laura S; Linehan, W Marston; Ballabio, Andrea. - In: EMBO MOLECULAR MEDICINE. - ISSN 1757-4684. - 15:5(2023). [10.15252/emmm.202216877]

TFEB and TFE3 drive kidney cystogenesis and tumorigenesis

Di Malta, Chiara;Vilardo, Claudia;Cinque, Laura;Sorrentino, Nicolina Cristina;Ballabio, Andrea
2023

Abstract

: Birt-Hogg-Dubé (BHD) syndrome is an inherited familial cancer syndrome characterized by the development of cutaneous lesions, pulmonary cysts, renal tumors and cysts and caused by loss-of-function pathogenic variants in the gene encoding the tumor-suppressor protein folliculin (FLCN). FLCN acts as a negative regulator of TFEB and TFE3 transcription factors, master controllers of lysosomal biogenesis and autophagy, by enabling their phosphorylation by the mechanistic Target Of Rapamycin Complex 1 (mTORC1). We have previously shown that deletion of Tfeb rescued the renal cystic phenotype of kidney-specific Flcn KO mice. Using Flcn/Tfeb/Tfe3 double and triple KO mice, we now show that both Tfeb and Tfe3 contribute, in a differential and cooperative manner, to kidney cystogenesis. Remarkably, the analysis of BHD patient-derived tumor samples revealed increased activation of TFEB/TFE3-mediated transcriptional program and silencing either of the two genes rescued tumorigenesis in human BHD renal tumor cell line-derived xenografts (CDXs). Our findings demonstrate in disease-relevant models that both TFEB and TFE3 are key drivers of renal tumorigenesis and suggest novel therapeutic strategies based on the inhibition of these transcription factors.
2023
TFEB and TFE3 drive kidney cystogenesis and tumorigenesis / Di Malta, Chiara; Zampelli, Angela; Granieri, Letizia; Vilardo, Claudia; De Cegli, Rossella; Cinque, Laura; Nusco, Edoardo; Pece, Salvatore; Tosoni, Daniela; Sanguedolce, Francesca; Sorrentino, Nicolina Cristina; Merino, Maria J; Nielsen, Deborah; Srinivasan, Ramaprasad; Ball, Mark W; Ricketts, Christopher J; Vocke, Cathy D; Lang, Martin; Karim, Baktiar; Lanfrancone, Luisa; Schmidt, Laura S; Linehan, W Marston; Ballabio, Andrea. - In: EMBO MOLECULAR MEDICINE. - ISSN 1757-4684. - 15:5(2023). [10.15252/emmm.202216877]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/919750
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