| Literature DB >> 25013076 |
Min Yu1, Aditya Bardia2, Nicola Aceto3, Francesca Bersani3, Marissa W Madden3, Maria C Donaldson3, Rushil Desai3, Huili Zhu3, Valentine Comaills3, Zongli Zheng4, Ben S Wittner3, Petar Stojanov5, Elena Brachtel6, Dennis Sgroi7, Ravi Kapur8, Toshihiro Shioda2, David T Ting2, Sridhar Ramaswamy2, Gad Getz9, A John Iafrate7, Cyril Benes2, Mehmet Toner10, Shyamala Maheswaran11, Daniel A Haber12.
Abstract
Circulating tumor cells (CTCs) are present at low concentrations in the peripheral blood of patients with solid tumors. It has been proposed that the isolation, ex vivo culture, and characterization of CTCs may provide an opportunity to noninvasively monitor the changing patterns of drug susceptibility in individual patients as their tumors acquire new mutations. In a proof-of-concept study, we established CTC cultures from six patients with estrogen receptor-positive breast cancer. Three of five CTC lines tested were tumorigenic in mice. Genome sequencing of the CTC lines revealed preexisting mutations in the PIK3CA gene and newly acquired mutations in the estrogen receptor gene (ESR1), PIK3CA gene, and fibroblast growth factor receptor gene (FGFR2), among others. Drug sensitivity testing of CTC lines with multiple mutations revealed potential new therapeutic targets. With optimization of CTC culture conditions, this strategy may help identify the best therapies for individual cancer patients over the course of their disease.Entities:
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Year: 2014 PMID: 25013076 PMCID: PMC4358808 DOI: 10.1126/science.1253533
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728