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1.
J Hematol Oncol ; 16(1): 112, 2023 11 21.
Artículo en Inglés | MEDLINE | ID: mdl-37990343

RESUMEN

Significant scientific advances in immunotherapy and targeted therapy approaches have improved clinical outcomes and increased treatment options for patients with genitourinary (GU) malignancies. We highlight the clinical trial developments released at the ASCO 2023 annual meeting, including PARP inhibitors for prostate cancer, antibody drug conjugates and fibroblast growth factor receptor inhibitors for urothelial cancer, and HIF2a inhibitors for renal cell carcinoma. Novel agents such as bispecific antibodies, chimeric antigen receptor T-cells, and radiopharmaceuticals are currently in early phase development and also have high potential impact for the GU cancer landscape. With more treatment options, the field will need to define best treatment sequencing to optimize outcomes for each patient.


Asunto(s)
Carcinoma de Células Renales , Inmunoconjugados , Neoplasias Renales , Neoplasias Urogenitales , Masculino , Humanos , Neoplasias Urogenitales/terapia , Inmunoconjugados/uso terapéutico , Inmunoterapia , Carcinoma de Células Renales/terapia , Neoplasias Renales/terapia
3.
J Virol ; 92(11)2018 06 01.
Artículo en Inglés | MEDLINE | ID: mdl-29514910

RESUMEN

Herpes simplex virus 1 (HSV-1) establishes a lifelong latent infection in host peripheral neurons, including the neurons of the trigeminal ganglia (TG). HSV-1 can reactivate from neurons to cause recurrent infection. During latency, the insulator protein CTCF occupies DNA binding sites on the HSV-1 genome, and these sites have been previously characterized as functional enhancer-blocking insulators. Previously, CTCF was found to be dissociated from wild-type virus postreactivation but not in mutants that do not reactivate, indicating that CTCF eviction may also be an important component of reactivation. To further elucidate the role of CTCF in reactivation of HSV-1, we used recombinant adeno-associated virus (rAAV) vectors to deliver a small interfering RNA targeting CTCF to peripheral neurons latent with HSV-1 in rabbit TG. Our data show that CTCF depletion resulted in long-term and persistent shedding of infectious virus in the cornea and increased ICP0 expression in the ganglia, indicating that CTCF depletion facilitates HSV-1 reactivation.IMPORTANCE Increasing evidence has shown that the insulator protein CTCF regulates gene expression of DNA viruses, including the gammaherpesviruses. While CTCF occupation and insulator function control gene expression in DNA viruses, CTCF eviction has been correlated to increased lytic gene expression and the dissolution of transcriptional domains. Our previous data have shown that in the alphaherpesvirus HSV-1, CTCF was found to be dissociated from the HSV-1 genome postreactivation, further indicating a global role for CTCF eviction in the transition from latency to reactivation in HSV-1 genomes. Using an rAAV8, we targeted HSV-1-infected peripheral neurons for CTCF depletion to show that CTCF depletion precedes the shedding of infectious virus and increased lytic gene expression in vivo, providing the first evidence that CTCF depletion facilitates HSV-1 reactivation.


Asunto(s)
Factor de Unión a CCCTC/genética , Técnicas de Inactivación de Genes/métodos , Herpes Simple/genética , Herpesvirus Humano 1/fisiología , Células 3T3 , Animales , Sitios de Unión , Factor de Unión a CCCTC/metabolismo , Córnea/virología , Modelos Animales de Enfermedad , Ganglios/virología , Genoma Viral , Herpes Simple/virología , Herpesvirus Humano 1/química , Ratones , Conejos , Activación Viral , Latencia del Virus , Esparcimiento de Virus
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