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Alternative to the soft-agar assay that permits high-throughput drug and genetic screens for cellular transformation
Author(s) -
Asaf Rotem,
Andreas Janzer,
Benjamin Izar,
Zhe Ji,
John G. Doench,
Levi A. Garraway,
Kevin Struhl
Publication year - 2015
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1505979112
Subject(s) - drug , high throughput screening , transformation (genetics) , drug discovery , computational biology , food and drug administration , biology , personalized medicine , gene , pharmacology , bioinformatics , genetics
Colony formation in soft agar is the gold-standard assay for cellular transformation in vitro, but it is unsuited for high-throughput screening. Here, we describe an assay for cellular transformation that involves growth in low attachment (GILA) conditions and is strongly correlated with the soft-agar assay. Using GILA, we describe high-throughput screens for drugs and genes that selectively inhibit or increase transformation, but not proliferation. Such molecules are unlikely to be found through conventional drug screening, and they include kinase inhibitors and drugs for noncancer diseases. In addition to known oncogenes, the genetic screen identifies genes that contribute to cellular transformation. Lastly, we demonstrate the ability of Food and Drug Administration-approved noncancer drugs to selectively kill ovarian cancer cells derived from patients with chemotherapy-resistant disease, suggesting this approach may provide useful information for personalized cancer treatment.

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