Different mutation profiles between epithelium and stroma in endometriosis and normal endometrium

被引:35
作者
Suda, Kazuaki [1 ]
Nakaoka, Hirofumi [2 ]
Yoshihara, Kosuke [1 ]
Ishiguro, Tatsuya [1 ]
Adachi, Sosuke [1 ]
Kase, Hiroaki [3 ]
Motoyama, Teiichi [4 ]
Inoue, Ituro [2 ]
Enomoto, Takayuki [1 ]
机构
[1] Niigata Univ, Dept Obstet & Gynecol, Grad Sch Med & Dent Sci, Niigata 9518510, Japan
[2] Natl Inst Genet, Div Human Genet, Mishima, Shizuoka 4118540, Japan
[3] Nagaoka Chuo Gen Hosp, Dept Obstet & Gynecol, Nagaoka, Niigata 9408653, Japan
[4] Niigata Univ, Grad Sch Med & Dent Sci, Dept Mol & Diagnost Pathol, Niigata 9518510, Japan
基金
日本学术振兴会;
关键词
stroma; epithelium; endometriosis; uterine endometrium; somatic mutation; target gene sequencing; ARID1A; CD10;
D O I
10.1093/humrep/dez155
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
STUDY QUESTION: Are there common mutation profiles between epithelial and stromal cells in ovarian endometriotic tissue and the normal endometrium? SUMMARY ANSWER: Our study revealed no common mutations between epithelial and stromal cells in ovarian endometriotic tissue and the normal endometrium. WHAT IS KNOWN ALREADY: Epithelial cells in both ovarian endometriotic tissue and the normal endometrium harbor somatic mutations in cancer-associated genes such as phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) and KRAS proto-oncogene, GTPase (KRAS). STUDY DESIGN, SIZE, DURATION: We performed a retrospective study to identify the mutation profiles of stromal cells in endometriotic tissue and the normal endometrium. We collected 11 endometriotic stroma samples and 10 normal endometrial stroma samples between 2013 and 2017 at a tertiary care center. PARTICIPANTS/MATERIALS, SETTING, METHODS: The laser microdissection method was used to obtain stromal cells in ovarian endometriotic and normal endometrial tissues from patients with ovarian endometriosis and/or other non-invasive gynecological diseases. Target gene sequencing was performed to assess and compare the mutation profiles of stromal cells with those of epithelial cells obtained in our previous study. For target gene sequencing, 76 genes were selected based on previous genomic analyses for ovarian endometriosis, normal endometnum, endometriosis-related ovarian cancer and endometrial cancer. MAIN RESULTS AND THE ROLE OF CHANCE: Stromal samples in ovarian endometrioma and normal endometrium harbor somatic mutations (18 mutations in 11 endometriosis samples and 16 mutations in 10 normal endometrial samples) but did not share any mutations with paired epithelial samples. The mutant allele frequency of stromal samples was significantly lower than that of epithelial samples in ovarian endometrioma (P = 6.0 x 10(-11)) and normal endometrium (P = 1.4 x 10(-7)). LIMITATIONS, REASONS FOR CAUTION: The number of genes evaluated in the mutational analysis was limited. Additionally, the functional roles of somatic mutations in stromal cells remain unclear. WIDER IMPLICATIONS OF THE FINDINGS: Different mutation profiles between paired epithelial and stromal cells in both ovarian endometrioma and normal endometrium suggest that origins of epithelial and stromal cells would be independent of each other in both normal endometrium and ovarian endometrioma; however, the theory of epithelial-mesenchymal transition is proposed in ovarian endometrioma.
引用
收藏
页码:1899 / 1905
页数:7
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