Endocrine-therapy-resistant ESR1 variants revealed by genomic characterization of breast-cancer-derived xenografts.

نویسندگان

  • Shunqiang Li
  • Dong Shen
  • Jieya Shao
  • Robert Crowder
  • Wenbin Liu
  • Aleix Prat
  • Xiaping He
  • Shuying Liu
  • Jeremy Hoog
  • Charles Lu
  • Li Ding
  • Obi L Griffith
  • Christopher Miller
  • Dave Larson
  • Robert S Fulton
  • Michelle Harrison
  • Tom Mooney
  • Joshua F McMichael
  • Jingqin Luo
  • Yu Tao
  • Rodrigo Goncalves
  • Christopher Schlosberg
  • Jeffrey F Hiken
  • Laila Saied
  • Cesar Sanchez
  • Therese Giuntoli
  • Caroline Bumb
  • Crystal Cooper
  • Robert T Kitchens
  • Austin Lin
  • Chanpheng Phommaly
  • Sherri R Davies
  • Jin Zhang
  • Megha Shyam Kavuri
  • Donna McEachern
  • Yi Yu Dong
  • Cynthia Ma
  • Timothy Pluard
  • Michael Naughton
  • Ron Bose
  • Rama Suresh
  • Reida McDowell
  • Loren Michel
  • Rebecca Aft
  • William Gillanders
  • Katherine DeSchryver
  • Richard K Wilson
  • Shaomeng Wang
  • Gordon B Mills
  • Ana Gonzalez-Angulo
  • John R Edwards
  • Christopher Maher
  • Charles M Perou
  • Elaine R Mardis
  • Matthew J Ellis
چکیده

To characterize patient-derived xenografts (PDXs) for functional studies, we made whole-genome comparisons with originating breast cancers representative of the major intrinsic subtypes. Structural and copy number aberrations were found to be retained with high fidelity. However, at the single-nucleotide level, variable numbers of PDX-specific somatic events were documented, although they were only rarely functionally significant. Variant allele frequencies were often preserved in the PDXs, demonstrating that clonal representation can be transplantable. Estrogen-receptor-positive PDXs were associated with ESR1 ligand-binding-domain mutations, gene amplification, or an ESR1/YAP1 translocation. These events produced different endocrine-therapy-response phenotypes in human, cell line, and PDX endocrine-response studies. Hence, deeply sequenced PDX models are an important resource for the search for genome-forward treatment options and capture endocrine-drug-resistance etiologies that are not observed in standard cell lines. The originating tumor genome provides a benchmark for assessing genetic drift and clonal representation after transplantation.

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عنوان ژورنال:
  • Cell reports

دوره 4 6  شماره 

صفحات  -

تاریخ انتشار 2013