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Chemical dissection of the cell cycle: probes for cell biology and anti-cancer drug development
Author(s) -
Silvia Senese,
YuChen Lo,
Dian Huang,
Thomas A. Zangle,
Ankur A. Gholkar,
L Robert,
Blanca Homet,
Antoni Ribas,
Matthew K. Summers,
Michael A. Teitell,
Robert Damoiseaux,
Jorge Z. Torres
Publication year - 2014
Publication title -
cell death and disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.482
H-Index - 111
ISSN - 2041-4889
DOI - 10.1038/cddis.2014.420
Subject(s) - cell cycle , cancer cell , mitosis , cell growth , biology , cell , cancer , drug discovery , microbiology and biotechnology , cell cycle checkpoint , cancer research , cell division , biochemistry , genetics
Cancer cell proliferation relies on the ability of cancer cells to grow, transition through the cell cycle, and divide. To identify novel chemical probes for dissecting the mechanisms governing cell cycle progression and cell division, and for developing new anti-cancer therapeutics, we developed and performed a novel cancer cell-based high-throughput chemical screen for cell cycle modulators. This approach identified novel G1, S, G2, and M-phase specific inhibitors with drug-like properties and diverse chemotypes likely targeting a broad array of processes. We further characterized the M-phase inhibitors and highlight the most potent M-phase inhibitor MI-181, which targets tubulin, inhibits tubulin polymerization, activates the spindle assembly checkpoint, arrests cells in mitosis, and triggers a fast apoptotic cell death. Importantly, MI-181 has broad anti-cancer activity, especially against BRAF V600E melanomas.

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