Despite recent advancements in the treatment of late-stage mutant BRAF V600E/K melanomas, a major hurdle continues to be acquired resistance to BRAF inhibitors such as vemurafenib. The mechanisms for resistance have proven to be heterogeneous, emphasizing the need to use broad therapeutic approaches. In this issue, the study “Stat3-targeted therapies overcome the acquired resistance to vemurafenib in melanomas” by Liu et al. proposes that signal transducer and activator of transcription 3 (STAT3)–paired box 3 (PAX3) signaling may be a mechanism that is used by melanomas to resist RAF inhibitors
BackgroundThe sustained clinical activity of the BRAF inhibitor vemurafenib (PLX4032/RG7204) in pati...
The identification of BRAF V600E as a driving mutation in approximately 50% of melanoma and the subs...
We generated cell lines resistant to BRAF inhibitors and show that the EGF receptor (EGFR)-SRC famil...
Despite recent advancements in the treatment of late-stage mutant BRAF V600E/K melanomas, a major hu...
Despite recent advancements in the treatment of late-stage mutant BRAF (V600E/K) melanomas, a major ...
Vemurafenib (PLX4032), a selective inhibitor of Braf, has been approved by the US Food and Drug Admi...
Rosalie Fisher, James LarkinDepartment of Medical Oncology, Royal Marsden Hospital, London, United K...
The RAS-RAF-MEK-ERK pathway is a key driver of proliferation and survival signals in tumor cells and...
Patients with advanced melanoma have traditionally had very poor prognosis. However, since 2011 bett...
The discovery of the BRAFV600E mutation led to the development of vemurafenib (PLX4032), a selective...
In the last four years, seven new drugs have been FDA approved for the treatment of late stage melan...
ABSTRACT Most melanomas harbor oncogenic BRAF V600 mutations, which constitutively acti-vate the MAP...
Background: The sustained clinical activity of the BRAF inhibitor vemurafenib (PLX4032/RG7204) in pa...
Malignant melanoma is the most aggressive form of skin cancer and has a very low survival rate. Over...
Metastatic melanoma (MM) presents a treatment challenge to oncologists worldwide. Dacarbazine is the...
BackgroundThe sustained clinical activity of the BRAF inhibitor vemurafenib (PLX4032/RG7204) in pati...
The identification of BRAF V600E as a driving mutation in approximately 50% of melanoma and the subs...
We generated cell lines resistant to BRAF inhibitors and show that the EGF receptor (EGFR)-SRC famil...
Despite recent advancements in the treatment of late-stage mutant BRAF V600E/K melanomas, a major hu...
Despite recent advancements in the treatment of late-stage mutant BRAF (V600E/K) melanomas, a major ...
Vemurafenib (PLX4032), a selective inhibitor of Braf, has been approved by the US Food and Drug Admi...
Rosalie Fisher, James LarkinDepartment of Medical Oncology, Royal Marsden Hospital, London, United K...
The RAS-RAF-MEK-ERK pathway is a key driver of proliferation and survival signals in tumor cells and...
Patients with advanced melanoma have traditionally had very poor prognosis. However, since 2011 bett...
The discovery of the BRAFV600E mutation led to the development of vemurafenib (PLX4032), a selective...
In the last four years, seven new drugs have been FDA approved for the treatment of late stage melan...
ABSTRACT Most melanomas harbor oncogenic BRAF V600 mutations, which constitutively acti-vate the MAP...
Background: The sustained clinical activity of the BRAF inhibitor vemurafenib (PLX4032/RG7204) in pa...
Malignant melanoma is the most aggressive form of skin cancer and has a very low survival rate. Over...
Metastatic melanoma (MM) presents a treatment challenge to oncologists worldwide. Dacarbazine is the...
BackgroundThe sustained clinical activity of the BRAF inhibitor vemurafenib (PLX4032/RG7204) in pati...
The identification of BRAF V600E as a driving mutation in approximately 50% of melanoma and the subs...
We generated cell lines resistant to BRAF inhibitors and show that the EGF receptor (EGFR)-SRC famil...