The introduction of v-raf murine sarcoma viral oncogene homolog B (BRAF) inhibitors in melanoma patients with BRAF (V600E) mutations has demonstrated significant clinical benefits. However, rarely do tumours regress completely. Frequently, the reason for this is that therapies targeting specific oncogenic mutations induce a number of intrinsic compensatory mechanisms, also known as adaptive responses or feedback loops, that enhance the pro-survival and pro-proliferative capacity of a proportion of the original tumour population, thereby resulting in tumour progression. In this review we will summarize the known adaptive responses that limit BRAF mutant therapy and discuss potential novel combinatorial therapies to overcome resistance
BRAF inhibitors elicit rapid antitumor responses in the majority of patients with BRAF(V600)-mutant ...
Cancer therapeutic regimens are gradually changing from using relatively unspecific cytotoxic agents...
Treatment of BRAF-mutant metastatic melanoma with mitogen-activated protein kinase (MAPK) pathway ta...
The discovery of activating mutations in BRAF at high frequency in cutaneous melanoma opened the doo...
Background The introduction of targeted therapies for the treatment of BRAF-mutant melanomas have im...
The discovery of activating mutations in BRAF at high frequency in cutaneous melanoma opened the doo...
The discovery of activating mutations in BRAF at high frequency in cutaneous melanoma opened the doo...
This systematic review investigated the literature on acquired v-raf murine sarcoma viral oncogene h...
BRAF inhibitor therapy may provide profound initial tumor regression in metastatic melanoma with BRA...
BRAF inhibitors elicit rapid antitumor responses in the majority of patients with BRAF V600-mutant m...
<div><p>Fifty percent of cutaneous melanomas are driven by activated <i>BRAF</i><sup>V600E</sup>, bu...
Understanding the role of mitogen-activated protein kinase (MAPK) pathway-activating mutations in th...
Since the discovery of BRAF mutations in over 50% of melanomas, various small molecule inhibitors ag...
BRAF inhibitors elicit rapid antitumor responses in the majority of patients with BRAF(V600)-mutant ...
Almost 50% of metastatic melanoma patients harbor a BRAF(V600) mutation and the introduction of BRAF...
BRAF inhibitors elicit rapid antitumor responses in the majority of patients with BRAF(V600)-mutant ...
Cancer therapeutic regimens are gradually changing from using relatively unspecific cytotoxic agents...
Treatment of BRAF-mutant metastatic melanoma with mitogen-activated protein kinase (MAPK) pathway ta...
The discovery of activating mutations in BRAF at high frequency in cutaneous melanoma opened the doo...
Background The introduction of targeted therapies for the treatment of BRAF-mutant melanomas have im...
The discovery of activating mutations in BRAF at high frequency in cutaneous melanoma opened the doo...
The discovery of activating mutations in BRAF at high frequency in cutaneous melanoma opened the doo...
This systematic review investigated the literature on acquired v-raf murine sarcoma viral oncogene h...
BRAF inhibitor therapy may provide profound initial tumor regression in metastatic melanoma with BRA...
BRAF inhibitors elicit rapid antitumor responses in the majority of patients with BRAF V600-mutant m...
<div><p>Fifty percent of cutaneous melanomas are driven by activated <i>BRAF</i><sup>V600E</sup>, bu...
Understanding the role of mitogen-activated protein kinase (MAPK) pathway-activating mutations in th...
Since the discovery of BRAF mutations in over 50% of melanomas, various small molecule inhibitors ag...
BRAF inhibitors elicit rapid antitumor responses in the majority of patients with BRAF(V600)-mutant ...
Almost 50% of metastatic melanoma patients harbor a BRAF(V600) mutation and the introduction of BRAF...
BRAF inhibitors elicit rapid antitumor responses in the majority of patients with BRAF(V600)-mutant ...
Cancer therapeutic regimens are gradually changing from using relatively unspecific cytotoxic agents...
Treatment of BRAF-mutant metastatic melanoma with mitogen-activated protein kinase (MAPK) pathway ta...