Clinical significance of pmTOR expression in endometrioid endometrial carcinoma

被引:13
作者
Choi, Chel Hun
Lee, Ji-Soo
Kim, Seong Rim [2 ]
Kim, Tae-Joong
Lee, Jeong-Won
Kim, Byoung-Gie
Bae, Duk-Soo [1 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Dept Obstet & Gynecol, Samsung Med Ctr, Seoul 135710, South Korea
[2] Medplan Pathol Lab Ctr, Dept Pathol, Seoul, South Korea
关键词
Endometrial cancer; pmTOR; Immunohistochemistry; GYNECOLOGIC-ONCOLOGY-GROUP; PHASE-III TRIAL; MAMMALIAN TARGET; CANCER; THERAPY; MTOR; ADENOCARCINOMA; CHEMOTHERAPY; RAPAMYCIN; SURGERY;
D O I
10.1016/j.ejogrb.2010.07.038
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: Endometrial adenocarcinoma has been proposed, due to frequent activation of the PI3K/A1Cr pathway, as a candidate neoplasm for treatment with mTOR inhibitors. However, data on the expression of mTOR in endometrial cancer are lacking. Study design: We used immunohistochemistry to evaluate the expression of pmTOR in 62 endometrial cancer surgical specimens. Results: The pmTOR protein was diffusely expressed in the cytoplasm of neoplastic epithelial cells, showing variable intensity. According to the chosen cutoff value, 34 (54.8%) out of 62 patients were scored as pmTOR-positive. pmTOR expression was significantly decreased in carcinomas with deep infiltration into the myometrium (P=.009), though it was not correlated with disease stage or lymph node metastasis. Univariate analysis showed that increased expression of pmTOR was significantly associated with better disease-free survival (P=.021). Conclusions: We show for the first time an association between pmTOR and better survival in patients with endometrial cancer. Future studies to stratify endometrial tumors by pmTOR status are needed. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:207 / 210
页数:4
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