Aberrant expression of p27(Kip1)-interacting cell-cycle regulatory proteins in ovarian clear cell carcinomas and their precursors with special consideration of two distinct multistage clear cell carcinogenetic pathways

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p27(Kip1)-interacting proteins are aberrantly expressed in ovarian clear cell carcinomas, with CCAF-associated tumors exhibiting slower cell-cycle progression than endometriosis-associated tumors.

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This study examined expression patterns of p27Kip1-interacting cell-cycle regulators (p27Kip1, Skp2, Cks1, cyclin A, cyclin E) and Ki-67 labeling index in 25 clear cell adenofibromas (benign and borderline) and 15 clear cell adenofibroma–associated clear cell adenocarcinomas, comparing them with previously studied endometriosis-associated clear cell adenocarcinomas. The authors found aberrant expression of these proteins overall more often in adenofibroma-associated cancers than in benign adenofibromas, with statistical significance only for Cks1 overexpression, and they observed lower frequencies of p27Kip1 downregulation, Skp2 overexpression, and cyclin A overexpression in adenofibroma-associated tumors versus endometriosis-associated tumors. Ki-67 labeling index increased along the benign→borderline→adenofibroma-associated cancer sequence, but the latter stages showed lower mean proliferation than atypical endometriosis components and endometriosis-associated cancers. The key limitation is that adenofibromas and adenofibroma-associated cancers are compared against a separate previously analyzed endometriosis-associated cohort rather than a fully contemporaneous unified dataset, which may constrain direct comparability. This paper directly relates to endometriosis by comparing cell-cycle regulator alterations across clear cell carcinogenesis pathways that include endometriosis-associated ovarian clear cell adenocarcinoma, and it discusses distinct multistage progression relative to atypical endometriosis components.

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Abstract

We have previously reported that alterations of p27(Kip1)-interacting cell-cycle proteins frequently occur during the development of endometriosis-associated ovarian clear cell adenocarcinoma (CCA; Yamamoto et al., Histopathology in press, 20). However, CCA also occurs in association with clear cell adenofibroma (CCAF). In this study, the expressions of p27(Kip1)-interacting proteins, i.e., p27(Kip1), Skp2, Cks1, cyclin A, cyclin E, and the Ki-67 labeling index (LI), were analyzed in 25 CCAFs (11 benign and 14 borderline) and 15 CCAF-associated CCAs, and compared with the expression status of each protein in the 23 previously studied endometriosis-associated CCAs. Although aberrant expression of all p27(Kip1)-interacting proteins was more frequent in the CCAF-associated CCAs than in the benign CCAFs, statistical significance was found only for Cks1 overexpression. The frequencies of p27(Kip1) downregulation and overexpression of Skp2 and cyclin A were significantly lower in CCAF-associated than in endometriosis-associated CCAs (P < 0.05, respectively). The frequencies of p27(Kip1) downregulation and Skp2 overexpression in borderline CCAFs were significantly lower than those in atypical endometriosis components in endometriosis-associated CCAs (P < 0.05, respectively). Mean Ki-67 LI increased significantly through benign (4.9%) to borderline (11.1%) CCAF and to CCAF-associated CCA (30.6%), but the latter two values were significantly lower than those in atypical endometriosis (21.4%) and endometriosis-associated CCA (46.9%; P < 0.05, respectively). These data suggest that accumulated alterations of p27(Kip1)-interacting proteins may accelerate the development of CCAs regardless of their carcinogenetic pathways, but that tumor cells in the CCAF-associated pathway appear to show slower cell-cycle progression than those in the endometriosis-associated pathway, possibly accounting for the distinct clinicopathological features of the two CCA subtypes.
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Abstract

We have previously reported that alterations of p27Kip1-interacting cell-cycle proteins frequently occur during the development of endometriosis-associated ovarian clear cell adenocarcinoma (CCA; Yamamoto et al., Histopathology in press, 20). However, CCA also occurs in association with clear cell adenofibroma (CCAF). In this study, the expressions of p27Kip1-interacting proteins, i.e., p27Kip1, Skp2, Cks1, cyclin A, cyclin E, and the Ki-67 labeling index (LI), were analyzed in 25 CCAFs (11 benign and 14 borderline) and 15 CCAF-associated CCAs, and compared with the expression status of each protein in the 23 previously studied endometriosis-associated CCAs. Although aberrant expression of all p27Kip1-interacting proteins was more frequent in the CCAF-associated CCAs than in the benign CCAFs, statistical significance was found only for Cks1 overexpression. The frequencies of p27Kip1 downregulation and overexpression of Skp2 and cyclin A were significantly lower in CCAF-associated than in endometriosis-associated CCAs (P < 0.05, respectively). The frequencies of p27Kip1 downregulation and Skp2 overexpression in borderline CCAFs were significantly lower than those in atypical endometriosis components in endometriosis-associated CCAs (P < 0.05, respectively). Mean Ki-67 LI increased significantly through benign (4.9%) to borderline (11.1%) CCAF and to CCAF-associated CCA (30.6%), but the latter two values were significantly lower than those in atypical endometriosis (21.4%) and endometriosis-associated CCA (46.9%; P < 0.05, respectively). These data suggest that accumulated alterations of p27Kip1-interacting proteins may accelerate the development of CCAs regardless of their carcinogenetic pathways, but that tumor cells in the CCAF-associated pathway appear to show slower cell-cycle progression than those in the endometriosis-associated pathway, possibly accounting for the distinct clinicopathological features of the two CCA subtypes. Similar content being viewed by others

References

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The authors are thankful to Ms. Kozue Suzuki for technical assistance with immunohistochemistry. Conflict of interest statement The authors declare no actual or potential conflicts of interest in this study. Author information Authors and Affiliations Corresponding author Rights and permissions About this article Cite this article Yamamoto, S., Tsuda, H., Miyai, K. et al. Aberrant expression of p27Kip1-interacting cell-cycle regulatory proteins in ovarian clear cell carcinomas and their precursors with special consideration of two distinct multistage clear cell carcinogenetic pathways. Virchows Arch 455, 413–422 (2009). https://doi.org/10.1007/s00428-009-0844-5 Received: Revised: Accepted: Published: Issue date: DOI: https://doi.org/10.1007/s00428-009-0844-5

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endometriosis

MeSH descriptors

Adenocarcinoma, Clear Cell Cell Cycle Proteins Cell Transformation, Neoplastic Intracellular Signaling Peptides and Proteins Ovarian Neoplasms Precancerous Conditions Adenocarcinoma, Clear Cell Adenocarcinoma, Clear Cell Adenocarcinoma, Clear Cell Adenofibroma Adenofibroma Adenofibroma Adenofibroma Cell Cycle Proteins Cell Cycle Proteins Cell Transformation, Neoplastic Cell Transformation, Neoplastic Cyclin-Dependent Kinase Inhibitor p27 Endometriosis Endometriosis

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