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Abstract
Aims
The
carcinogenesis of ovarian clear cell carcinoma (CCC) has been
hypothesized to comprise two different pathways: an adenofibroma-carcinoma sequence and an endometriosis-carcinoma sequence.
However, the difference in the genetic basis of these two pathways
remains unclear. Recent studies have suggested that an ARID1A mutation
and the loss of the corresponding protein, BAF250a, are frequent events
in CCC. Herein, we investigated the difference in the loss of BAF250a
expression in adenofibroma-related CCC and endometriosis-related CCC.
Methods and Results
In
total, 93 cases of surgically treated CCC were evaluated. The presence
of adenofibroma and endometriosis associated with carcinoma was
determined by reviewing hematoxylin and eosin-stained slides for each
case. BAF250a expression in carcinoma was examined
immunohistochemically. The loss of BAF250a expression was detected in
carcinomas in 50 of 93 (54%) cases, including 5/18 (28%) with adenofibroma alone, 30/45 (67%) with endometriosis alone, 8/18 (44%) with both conditions, and 7/12 (58%)
with neither condition. The loss of BAF250a expression was
significantly less frequent in CCC cases with adenofibroma than in cases
with endometriosis (p = 0.01, Fisher's exact test).
Conclusions
The action of ARID1A in carcinogenesis differs between adenofibroma-related CCC and endometriosis-related CCC.
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