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Author Correction: The genomic landscape of response to EGFR blockade in colorectal cancer - Nature
Correction to: Nature https://doi.org/10.1038/nature14969 Published online 30 September 2015 In Extended Data Fig. 8 of this article, a micrograph shown in the left column (panel AZD) was inadvertently duplicated during figure preparation. The intended image was meant to show phospho-ERK (P-ERK) levels in a MAP2K1-mutant patient-derived xenograft (PDX) exposed to the MEK inhibitor AZD6244 (AZD). However, this image was accidentally overlaid with a micrograph from Extended Data Fig.
Colorectal cancer residual disease at maximal response to EGFR blockade displays a druggable Paneth cell-like phenotype
Tumor cells hunker down to escape Targeted therapy inhibiting pathways involved in tumor growth is becoming increasingly common. This includes inhibitors of the epidermal growth factor receptor, which are used for a variety of tumor types including colorectal cancer. Unfortunately, the treatment’s effects are often incomplete such that residual cancer cells stay behind and contribute to relapse. Lupo et al.
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