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ABSTRACT: Background
Most pelvic high-grade serous (HGS) carcinomas have been proposed to arise from tubal primaries that progress rapidly to advanced disease. However, the temporal sequence of ovarian and peritoneal metastases is not well characterized.Methods
To establish the sequence of metastases, phylogenetic relationships among the ovarian and peritoneal carcinomas were determined from single-nucleotide variations (SNVs) in nine tumor regions from each patient with pelvic HGS carcinomas. Somatic SNVs from each tumor sample were used to reconstruct phylogenies of samples from each patient. Variant allele frequencies were used to reconstruct subclone phylogenies in each tumor sample.Results
We show that pelvic HGS carcinomas are highly heterogeneous, only sharing less tha
SUBMITTER: Chien J
PROVIDER: S-EPMC5858520 | biostudies-literature | 2018
REPOSITORIES: biostudies-literature