Val600Glu (V600E) mutation is the most common BRAF mutation detected in thyroid cancer. Hence, recent research efforts have been performed trying to explore several inhibitors of the V600E mutation-containing BRAF kinase as potential therapeutic options in thyroid cancer refractory to standard interventions. Among them, vemurafenib is a selective BRAF inhibitor approved by FDA for clinical practice. Unfortunately, vemurafenib often displays limited efficacy in poorly differentiated and anaplastic thyroid carcinomas probably because of intrinsic and/or acquired resistance mechanisms. In this view, cancer stem cells may represent a possible mechanism of resistance to vemurafenib, due to their self-renewal and chemo resistance properties
SummaryDespite the development of potent RAF/mitogen-activated protein kinase (MAPK) pathway inhibit...
Although recent clinical trials of BRAF inhibitor combinations have demonstrated improved efficacy i...
Recent data implicate elevated transforming growth factor-β (TGFβ) signalling in BRAF inhibitor drug...
Val600Glu (V600E) mutation is the most common BRAF mutation detected in thyroid cancer. Hence, recen...
Purpose: Papillary thyroid carcinoma (PTC) is the most frequent endocrine tumor. BRAFV600Erepresents...
BRAFV600E mutation exerts an essential oncogenic function in many tumors, including papillary thyroi...
Background: BRAF inhibitors are effective anticancer agents in BRAF-mutated melanomas. By contrast, ...
The Kirsten rat sarcoma viral oncogene homolog (RAS)/v-raf-1 murine leukemia viral oncogene homolog ...
Clinical studies evaluating targeted BRAFV600E inhibitors in advanced thyroid cancer patients are cu...
의과대학/박사BRAF (V600E) mutation is the most commonly detected genetic alteration in thyroid cancer. Unl...
Purpose: Anaplastic thyroid cancer (ATC) is rare but with poor prognosis. TRAIL can selectively indu...
BRAF is a major oncoprotein and oncogenic mutations in BRAF are found in a significant number of can...
Resistance to the BRAF inhibitor vemurafenib poses a significant problem for the treatment of BRAFV6...
BRAF (V600E) mutation is the most commonly detected genetic alteration in thyroid cancer. Unlike its...
Although recent clinical trials of BRAF inhibitor combinations have demonstrated improved efficacy i...
SummaryDespite the development of potent RAF/mitogen-activated protein kinase (MAPK) pathway inhibit...
Although recent clinical trials of BRAF inhibitor combinations have demonstrated improved efficacy i...
Recent data implicate elevated transforming growth factor-β (TGFβ) signalling in BRAF inhibitor drug...
Val600Glu (V600E) mutation is the most common BRAF mutation detected in thyroid cancer. Hence, recen...
Purpose: Papillary thyroid carcinoma (PTC) is the most frequent endocrine tumor. BRAFV600Erepresents...
BRAFV600E mutation exerts an essential oncogenic function in many tumors, including papillary thyroi...
Background: BRAF inhibitors are effective anticancer agents in BRAF-mutated melanomas. By contrast, ...
The Kirsten rat sarcoma viral oncogene homolog (RAS)/v-raf-1 murine leukemia viral oncogene homolog ...
Clinical studies evaluating targeted BRAFV600E inhibitors in advanced thyroid cancer patients are cu...
의과대학/박사BRAF (V600E) mutation is the most commonly detected genetic alteration in thyroid cancer. Unl...
Purpose: Anaplastic thyroid cancer (ATC) is rare but with poor prognosis. TRAIL can selectively indu...
BRAF is a major oncoprotein and oncogenic mutations in BRAF are found in a significant number of can...
Resistance to the BRAF inhibitor vemurafenib poses a significant problem for the treatment of BRAFV6...
BRAF (V600E) mutation is the most commonly detected genetic alteration in thyroid cancer. Unlike its...
Although recent clinical trials of BRAF inhibitor combinations have demonstrated improved efficacy i...
SummaryDespite the development of potent RAF/mitogen-activated protein kinase (MAPK) pathway inhibit...
Although recent clinical trials of BRAF inhibitor combinations have demonstrated improved efficacy i...
Recent data implicate elevated transforming growth factor-β (TGFβ) signalling in BRAF inhibitor drug...