TY - JOUR
T1 - Deep Clonal Profiling of Formalin Fixed Paraffin Embedded Clinical Samples
AU - Holley, Tara
AU - Lenkiewicz, Elizabeth
AU - Evers, Lisa
AU - Tembe, Waibhav
AU - Ruiz, Christian
AU - Gsponer, Joel R.
AU - Rentsch, Cyrill A.
AU - Bubendorf, Lukas
AU - Stapleton, Mark
AU - Amorese, Doug
AU - Legendre, Christophe
AU - Cunliffe, Heather E.
AU - McCullough, Ann E.
AU - Pockaj, Barbara
AU - Craig, David
AU - Carpten, John
AU - Von Hoff, Daniel
AU - Iacobuzio-Donahue, Christine
AU - Barrett, Michael T.
PY - 2012/11/30
Y1 - 2012/11/30
N2 - Formalin fixed paraffin embedded (FFPE) tissues are a vast resource of annotated clinical samples. As such, they represent highly desirable and informative materials for the application of high definition genomics for improved patient management and to advance the development of personalized therapeutics. However, a limitation of FFPE tissues is the variable quality of DNA extracted for analyses. Furthermore, admixtures of non-tumor and polyclonal neoplastic cell populations limit the number of biopsies that can be studied and make it difficult to define cancer genomes in patient samples. To exploit these valuable tissues we applied flow cytometry-based methods to isolate pure populations of tumor cell nuclei from FFPE tissues and developed a methodology compatible with oligonucleotide array CGH and whole exome sequencing analyses. These were used to profile a variety of tumors (breast, brain, bladder, ovarian and pancreas) including the genomes and exomes of matching fresh frozen and FFPE pancreatic adenocarcinoma samples.
AB - Formalin fixed paraffin embedded (FFPE) tissues are a vast resource of annotated clinical samples. As such, they represent highly desirable and informative materials for the application of high definition genomics for improved patient management and to advance the development of personalized therapeutics. However, a limitation of FFPE tissues is the variable quality of DNA extracted for analyses. Furthermore, admixtures of non-tumor and polyclonal neoplastic cell populations limit the number of biopsies that can be studied and make it difficult to define cancer genomes in patient samples. To exploit these valuable tissues we applied flow cytometry-based methods to isolate pure populations of tumor cell nuclei from FFPE tissues and developed a methodology compatible with oligonucleotide array CGH and whole exome sequencing analyses. These were used to profile a variety of tumors (breast, brain, bladder, ovarian and pancreas) including the genomes and exomes of matching fresh frozen and FFPE pancreatic adenocarcinoma samples.
UR - http://www.scopus.com/inward/record.url?scp=84870626661&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84870626661&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0050586
DO - 10.1371/journal.pone.0050586
M3 - Article
C2 - 23226320
AN - SCOPUS:84870626661
SN - 1932-6203
VL - 7
JO - PLoS One
JF - PLoS One
IS - 11
M1 - e50586
ER -