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. 2014 Jul 2;6(243):243fs26.
doi: 10.1126/scitranslmed.3009586.

Functional genomics for personalized cancer therapy

Affiliations

Functional genomics for personalized cancer therapy

Jeffrey W Tyner. Sci Transl Med. .

Abstract

Integration of functional and genomic screening strategies reveals clinically actionable genetic events that impact the effectiveness of cancer treatment regimens and the outcomes of cancer patients.

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Conflict of interest statement

I have received research funding from Incyte Pharmaceuticals. A patent is pending on the use of CSF3R mutation as a diagnostic tool in hematologic malignancies.

Figures

Fig. 1
Fig. 1. Functional genomics approach: current and future
To comprehensively define the functional genomic landscape of cancer, we are currently performing parallel analyses of primary specimens from patients with hematologic malignancies. Genomic analysis reveals a large number of genetic events, most of which are seen in very small fractions of patients. Functional screening shows heterogeneous patterns of drug sensitivity with unclear genetic etiology. By integrating these data streams, we have identified pathogenetically important and clinically actionable genetic events, such as dependence on ROR1 and the pre–B cell receptor in t(1;19)-ALL and mutant CSF3R signaling in CNL. As we learn more from this platform, we build toward a future in which personalized, targeted therapies are prescribed solely on the basis of rapid genomic analysis of individual patient tumor specimens.

References

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