Abstract
E7107 is a derivative of the pladienolide family of natural product spliceosome inhibitors, which targets the U2 small nuclear ribonucleoprotein (snRNP) subunit SF3b. The results of a first-in-human trial with E7107 have been reported, representing an important translational step toward the goal of modulating RNA splicing for cancer therapy.
Original language | English (US) |
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Pages (from-to) | 6064-6066 |
Number of pages | 3 |
Journal | Clinical Cancer Research |
Volume | 19 |
Issue number | 22 |
DOIs | |
State | Published - Nov 15 2013 |