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The genomic trajectory of ovarian high-grade serous carcinoma can be observed in STIC lesions.
- Source :
-
The Journal of pathology [J Pathol] 2024 Sep; Vol. 264 (1), pp. 42-54. Date of Electronic Publication: 2024 Jul 02. - Publication Year :
- 2024
-
Abstract
- Ovarian high-grade serous carcinoma (HGSC) originates in the fallopian tube, with secretory cells carrying a TP53 mutation, known as p53 signatures, identified as potential precursors. p53 signatures evolve into serous tubal intraepithelial carcinoma (STIC) lesions, which in turn progress into invasive HGSC, which readily spreads to the ovary and disseminates around the peritoneal cavity. We recently investigated the genomic landscape of early- and late-stage HGSC and found higher ploidy in late-stage (median 3.1) than early-stage (median 2.0) samples. Here, to explore whether the high ploidy and possible whole-genome duplication (WGD) observed in late-stage disease were determined early in the evolution of HGSC, we analysed archival formalin-fixed paraffin-embedded (FFPE) samples from five HGSC patients. p53 signatures and STIC lesions were laser-capture microdissected and sequenced using shallow whole-genome sequencing (sWGS), while invasive ovarian/fallopian tube and metastatic carcinoma samples underwent macrodissection and were profiled using both sWGS and targeted next-generation sequencing. Results showed highly similar patterns of global copy number change between STIC lesions and invasive carcinoma samples within each patient. Ploidy changes were evident in STIC lesions, but not p53 signatures, and there was a strong correlation between ploidy in STIC lesions and invasive ovarian/fallopian tube and metastatic samples in each patient. The reconstruction of sample phylogeny for each patient from relative copy number indicated that high ploidy, when present, occurred early in the evolution of HGSC, which was further validated by copy number signatures in ovarian and metastatic tumours. These findings suggest that aberrant ploidy, suggestive of WGD, arises early in HGSC and is detected in STIC lesions, implying that the trajectory of HGSC may be determined at the earliest stages of tumour development. © 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.<br /> (© 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.)
- Subjects :
- Humans
Female
Carcinoma in Situ genetics
Carcinoma in Situ pathology
Neoplasm Grading
DNA Copy Number Variations
Mutation
Genomics methods
Whole Genome Sequencing
Ploidies
Middle Aged
Biomarkers, Tumor genetics
Disease Progression
Ovarian Neoplasms genetics
Ovarian Neoplasms pathology
Cystadenocarcinoma, Serous genetics
Cystadenocarcinoma, Serous pathology
Fallopian Tube Neoplasms genetics
Fallopian Tube Neoplasms pathology
Tumor Suppressor Protein p53 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1096-9896
- Volume :
- 264
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- The Journal of pathology
- Publication Type :
- Academic Journal
- Accession number :
- 38956451
- Full Text :
- https://doi.org/10.1002/path.6322