Association of circulating Progesterone Receptor Membrane Component-1 (PGRMC1) with PGRMC1 expression in breast tumour tissue and with clinical breast tumour characteristics

被引:11
作者
Cai, Guiju [1 ]
Yang, Xue [2 ]
Ruan, Xiangyan [1 ,3 ,4 ]
Wang, Jing [2 ]
Fang, Yi [2 ]
Wei, Yun [5 ]
Zhang, Ying [1 ]
Gu, Muqing [1 ]
Mueck, Alfred O. [1 ,3 ,4 ]
机构
[1] Capital Med Univ, Beijing Obstet & Gynecol Hosp, Dept Gynecol Endocrinol, 251 Yaojiayuan Rd, Beijing 100026, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Canc Hosp, Natl Clin Res Ctr Canc, Breast Surg Oncol,Natl Canc Ctr, Beijing 100021, Peoples R China
[3] Univ Tubingen, Dept Womens Hlth, Univ Womens Hosp, Tubingen, Germany
[4] Univ Tubingen, Dept Womens Hlth, Res Ctr Womens Hlth, Tubingen, Germany
[5] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
Blood assessment; Breast cancer risk; PGRMC1; expression; ESTROGEN PLUS PROGESTIN; HEME-1 DOMAIN PROTEIN; CANCER-CELLS; PROLIFERATION; GROWTH; BENEFITS; INCREASE; RISKS;
D O I
10.1016/j.maturitas.2020.06.008
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Objectives: Progesterone receptor membrane component-1 (PGRMC1) in breast cancer tissue has been suggested to predict a worse prognosis. The aim of this study was to assess for the first time whether PGRMC1 expressed in cancer tissue is associated with PGRMC1 blood concentrations and whether both are correlated with clinical tumour characteristics known to predict a worse outcome. Methods: In total, 201 patients with invasive breast cancer and 65 with benign breast disease (control group) were recruited. PGRMC1 blood concentrations were measured by a recently developed ELISA, PGRMC1 in breast cancer tissue was assessed by immunohistochemistry, and the correlation between the two was calculated. Receiver-operating characteristic (ROC) curve analysis was used to assess area under the curve (AUC). Furthermore, PGRMC1 was correlated with tumour characteristics such as tumour diameter, tumour grade and metastatic status, and with known blood tumour markers. Results: AUC for the breast cancer group was 0.713, which was significantly higher than in the control group (p < 0.01). Blood PGRMC1 concentrations had a strong (positive) correlation with tissue PGRMC1 expression (p < 0.01) but were not associated with serum tumour markers CEA, CA125, CA153 and TPS. Tissue PGRMC1, ER and cancer stage were positively associated with blood PGRMC1 (p < 0.05). Conclusions: As PGRMC1 expression levels in cancer tissue were significantly correlated with PGRMC1 in blood, and because concentrations in blood were also positively associated with breast tumour characteristics known to predict a worse prognosis, PGRMC1 may be valuable as a new tumour marker and may be superior to known tumour markers such as CEA, CA125, CA153 and TPS.
引用
收藏
页码:64 / 71
页数:8
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