An allelotype analysis indicating the presence of two distinct ovarian clear-cell carcinogenic pathways: endometriosis-associated pathway vs. clear-cell adenofibroma-associated pathway

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Allele loss analysis of ovarian clear-cell adenocarcinomas indicated distinct genetic pathways for those associated with endometriosis versus clear-cell adenofibroma, with specific chromosomal loci differing between the two groups.

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The paper performed an allelotype (loss of heterozygosity, LOH) analysis of ovarian clear-cell adenocarcinomas to compare two proposed carcinogenic routes: endometriosis-associated carcinomas (20 cases) versus clear-cell adenofibroma-associated carcinomas (14 cases). LOH was assessed at 24 polymorphic loci across 12 chromosomal arms, and overall LOH frequencies were similar between groups, while specific loci differed, with LOH at chromosomes 3p, 5q, and 11q occurring at significantly higher frequencies in the endometriosis-associated tumors (P = 0.026, 0.007, and 0.011). Immunohistochemistry showed a close association between allelic status at the 3p25–26 locus and von Hippel–Lindau (VHL) protein expression (P = 0.0026), supporting two distinct pathways. The study’s explicit limitation is the case-based categorization into precursor pathways without direct precursor lesion sampling, and the analysis is restricted to LOH at predefined loci. This paper is centrally about endometriosis — it compares an endometriosis-associated ovarian clear-cell carcinoma pathway against a clear-cell adenofibroma-associated pathway using LOH patterns and VHL-related findings.

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Abstract

Patterns of allele loss (loss of heterozygosity (LOH)) were studied to identify the genetic backgrounds underlying the two putative carcinogenic pathways of ovarian clear-cell adenocarcinoma: carcinomas thought to arise in endometriosis (endometriosis-associated carcinomas, 20 cases) and carcinomas thought to be derived from clear-cell adenofibroma ((CCAF)-associated carcinomas, 14 cases). Each tumor was assessed for LOH at 24 polymorphic loci located on 12 chromosomal arms: 1p, 3p, 5q, 8p, 9p, 10q, 11q, 13q, 17p, 17q, 19p, and 22q. For all informative loci, the frequency of LOH was not statistically different between the two carcinoma groups: 38% (66/172 loci) in the endometriosis-associated carcinomas and 35% (40/113 loci) in the CCAF-associated carcinomas. In the endometriosis-associated carcinomas, LOH was detected at high frequencies (>50%) at 3p, 5q, and 11q and at low frequencies (<20%) at 8p, 13q, and 17p. In the CCAF-associated carcinomas, LOH was detected at high frequencies at 1p, 10q, and 13q and at low frequencies at 3p, 9p, 11q, and 17q. The frequencies of LOH at chromosomes 3p, 5q, and 11q were significantly higher in the endometriosis-associated carcinomas than in the CCAF-associated carcinomas (P = 0.026, 0.007, and 0.011, respectively). Immunohistochemical analysis demonstrated a close association between the allelic status of the 3p25–26 locus and levels of von Hippel–Lindau (VHL) protein expression (P = 0.0026). These data further support the presence of two distinct carcinogenic pathways to ovarian clear-cell adenocarcinoma; the allelic status of the 3p, 5q, and 11q loci may provide a means to identify the precursor lesions of these carcinomas. Similar content being viewed by others

References

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An allelotype analysis indicating the presence of two distinct ovarian clear-cell carcinogenic pathways: endometriosis-associated pathway vs. clear-cell adenofibroma-associated pathway. Virchows Arch 455, 261–270 (2009). https://doi.org/10.1007/s00428-009-0816-9 Received: Revised: Accepted: Published: Issue date: DOI: https://doi.org/10.1007/s00428-009-0816-9

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endometriosis

MeSH descriptors

Adenocarcinoma, Clear Cell Adenocarcinoma, Clear Cell Adenofibroma Endometriosis Loss of Heterozygosity Ovarian Neoplasms Adenocarcinoma, Clear Cell Adenocarcinoma, Clear Cell Adenofibroma Alleles Endometriosis Female Humans Hypoxia-Inducible Factor 1, alpha Subunit Hypoxia-Inducible Factor 1, alpha Subunit Immunohistochemistry Ovarian Neoplasms Ovarian Neoplasms Ovarian Neoplasms Von Hippel-Lindau Tumor Suppressor Protein

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