GAL3 Protein Expression is Related to Clinical Features of Prolactin-Secreting Pituitary Microadenoma and Predicts its Recurrence after Surgical Treatment

被引:6
作者
Dai, Dongwei [1 ]
Li, Ya'nan [1 ]
Lu, Qiong [2 ]
Yu, Longyang [1 ]
Min, Weijie [1 ]
Wang, Laixing [1 ]
Cao, Yiqun [1 ]
Yue, Zhijian [1 ]
机构
[1] Second Mil Med Univ, Changhai Hosp, Dept Neurosurg, Shanghai 200433, Peoples R China
[2] Second Mil Med Univ, Changhai Hosp, Dept Lab Med, Shanghai 200433, Peoples R China
关键词
Galectin-3; Pituitary adenomas; Prognosis; GALECTIN-3; EXPRESSION; DIFFERENTIAL EXPRESSION; CHINESE PATIENTS; BLADDER-CANCER; CARCINOMA; TUMORS; ADENOMAS; LECTINS; MICE; HYPERPLASIA;
D O I
10.1159/000358673
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Previous in vitro study showed that Galectin-3 (Gal-3) protein plays an important role in pituitary tumorigenesis, however, the association of Gal-3 expression with the clinical feature and prognosis of pituitary tumor in a clinical setting remains unknown. Methods: We enrolled 220 patients with prolactin-secreting pituitary adenomas (PA) who previously had transsphenoidal pituitary surgery. The Gal-3 expression was detected in the patients' PA samples using immunohistochemistry and those patients were followed up. A prolactin-secreting PA cell line, the MMQ cell line, was used to study the in vitro effect of Gal-3 on proliferation, migration and invasion of PA cells using small interfering RNA (siRNA) transfecton technique. The in vivo tumorgenesis in nude mice was also studied. Results: We found that Gal-3 expression was not related to age and sex, but positively associated with tumor invasion (P < 0.001), tumor sizes (P < 0.001) and pre-operative prolactin levels (P < 0.001). The multivariate Cox analysis showed that the Gal-3 expression was closely associated with the recurrence of PA after the surgical treatment (HR = 3.15, P = 0.002). The in vitro studies showed that Gal-3 knock-down by the siRNA technique significantly inhibited the proliferation, migration and invasion ability of the MMQ cells, whereas Gal-3 siRNA transfection induced apoptosis of the MMQ cells. The in vivo tumorgenesis assay showed that Gal-3 siRNA transfection significantly inhibited the tumor volume in vivo compared to transfection of the control siRNA (P < 0.001). Conclusion: Gal-3 regulates proliferation, apoptosis, migration and invasion of the MMQ cells. Gal-3 may be used as a tissue marker to evaluate the clinical feature and prognosis of PA patients. Copyright (C) 2014 S. Karger AG, Basel
引用
收藏
页码:1026 / 1035
页数:10
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