Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jacob L. Schillo"'
Publikováno v:
iScience, Vol 26, Iss 10, Pp 107805- (2023)
Summary: Combined BRAF and MEK inhibition is an effective treatment for BRAF-mutant cutaneous melanoma. However, most patients progress on this treatment due to drug resistance. Here, we applied the Sleeping Beauty transposon system to understand how
Externí odkaz:
https://doaj.org/article/307a6faef0774c0fa828d7bf2cb30974
Autor:
Adam J. Dupuy, Christopher S. Stipp, Jesse D. Riordan, Jeremy Bobera, Sarah A. Mullen, Brooke M. Jennings, Eliot Y. Zhu, Andrew P. Voigt, Lexy S. Wadsworth, Hayley R. Vaughn, Afshin Varzavand, Jacob L. Schillo, Charlotte R. Feddersen
The use of selective BRAF inhibitors (BRAFi) has produced remarkable outcomes for patients with advanced cutaneous melanoma harboring a BRAFV600E mutation. Unfortunately, the majority of patients eventually develop drug-resistant disease. We employed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6eaeb0dd15610b75d4835c5c2b200b47
https://doi.org/10.1158/0008-5472.c.6510806
https://doi.org/10.1158/0008-5472.c.6510806
Autor:
Adam J. Dupuy, Christopher S. Stipp, Jesse D. Riordan, Jeremy Bobera, Sarah A. Mullen, Brooke M. Jennings, Eliot Y. Zhu, Andrew P. Voigt, Lexy S. Wadsworth, Hayley R. Vaughn, Afshin Varzavand, Jacob L. Schillo, Charlotte R. Feddersen
Supplemental figures showing more detailed analysis of the genetic screen results (S1-S3), additional experiments showing biological validation of major candidate genes (S4-S7), and characterization of spontaneous Vemurafenib resistance in A375 cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::763c2810c62639764eae9b5898ddc732
https://doi.org/10.1158/0008-5472.22420994
https://doi.org/10.1158/0008-5472.22420994
Autor:
Adam J. Dupuy, Christopher S. Stipp, Jesse D. Riordan, Jeremy Bobera, Sarah A. Mullen, Brooke M. Jennings, Eliot Y. Zhu, Andrew P. Voigt, Lexy S. Wadsworth, Hayley R. Vaughn, Afshin Varzavand, Jacob L. Schillo, Charlotte R. Feddersen
This file contains 4 supplemental tables.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bb40e1219583d6c2b577a68cb4a9de0
https://doi.org/10.1158/0008-5472.22420997.v1
https://doi.org/10.1158/0008-5472.22420997.v1
Autor:
Jeremy Bobera, Charlotte R. Feddersen, Sarah A. Mullen, Jesse D. Riordan, Lexy S. Wadsworth, Jacob L. Schillo, Adam J. Dupuy, Hayley R. Vaughn, Christopher S. Stipp, Brooke M. Jennings, Andrew P. Voigt, Afshin Varzavand, Eliot Y. Zhu
Publikováno v:
Cancer Research. 79:5074-5087
The use of selective BRAF inhibitors (BRAFi) has produced remarkable outcomes for patients with advanced cutaneous melanoma harboring a BRAFV600E mutation. Unfortunately, the majority of patients eventually develop drug-resistant disease. We employed
Autor:
Charlotte R. Feddersen, Hayley R. Vaughn, Jesse D. Riordan, Eliot Y. Zhu, Andrew Voight, Afshin Varzavand, Jacob L. Schillo, Christopher S. Stipp, Adam J. Dupuy
Publikováno v:
Cancer Research. 80:PR17-PR17
BRAF/MEK inhibition remains an important treatment option for patients with BRAF V600 mutant melanoma who show disease progression on immunotherapy; however, the majority of patients treated with BRAF/MEK (MAPKi) therapy develop MAPKi-resistant disea
Autor:
Eliot Y. Zhu, Christopher S. Stipp, Lexy S. Wadsworth, Afshin Varzavand, Adam J. Dupuy, Hayley R. Vaughn, Charlotte R. Feddersen, Jacob L. Schillo, Andrew P. Voigt, Jesse D. Riordan
Publikováno v:
Cancer Research. 80:B08-B08
The serine/threonine protein kinase BRAF is mutated in approximately 50% of cutaneous melanomas, leading to hyperactivation of the MAPK/ERK pathway. The most common mutations, BRAFV600, can be targeted by selective kinase inhibitors, such as vemurafe
Autor:
Adam J. Dupuy, Hayley R. Vaughn, Charlotte R. Feddersen, Andrew P. Voigt, Lexy S. Wadsworth, Jacob L. Schillo, Christopher S. Stipp, Eliot Y. Zhu
Publikováno v:
Cancer Research. 78:LB-096
Melanoma is the deadliest form of skin cancer, and until recently patients had few treatment options upon diagnosis. Fortunately, this lack of treatment options changed with the discovery of vemurafenib, a highly selective kinase inhibitor that speci