with Japanese or Endometriosis in Ovarian
article
OA: closed
CC0
AI-generated summary
This study used CGH to identify copy number alterations in ovarian clear cell adenocarcinoma, finding amplification of chromosome 8 and 20q13.2 including ZNF217 linked to its clinical characteristics.
One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works
Abstract
When compared with other epithelial ovarian cancers, the clinical characteristics of ovarian clear cell adenocarcinoma (CCC) include 1) a higher incidence among Japanese, 2) an as-sociation with endometriosis, 3) poor prognosis in advanced stages, and 4) a higher inci-dence of thrombosis as a complication. We used high resolution comparative genomic hybridization (CGH) to identify somatic copy number alterations (SCNAs) associated with each of these clinical characteristics of CCC. The Human Genome CGH 244A Oligo Micro-array was used to examine 144 samples obtained from 120 Japanese, 15 Korean, and nine German patients with CCC. The entire 8q chromosome (minimum corrected p-value: q = 0.0001) and chromosome 20q13.2 including the ZNF217 locus (q = 0.0078) were amplified
My notes (saved in your browser only)
Condition tags
Citation neighborhood (no data yet)
We don't have any in-corpus citations linked to this paper yet. The paper's references may be in our DB but unresolved to ``paper_id`` (resolution happens at ingest when the cited DOI matches a row we already have). Run the cross-source citation reconcile pass to retry.
Source provenance
- openalex
- last seen: 2026-05-10T11:03:09.910718+00:00
License: CC0
· commercial use OK