Zhu Haibo, Yao Xiaohui, Wu Lijuan, Li Chuzhong, Bai Jiwei, Gao Hua, Ji Hongming, Zhang Yazhuo
Beijing Neurosurgical Institute, Capital Medical University, Beijing, China.
Shanxi Provincial People's Hospital, Taiyuan, Shanxi, China.
World Neurosurg. 2018 Nov;119:e23-e31. doi: 10.1016/j.wneu.2018.06.154. Epub 2018 Jun 30.
This study was undertaken primarily to research transforming growth factor β1 (TGF-β1) and Wnt inhibitory factor 1 (WIF1) for the prediction of nonfunctioning pituitary adenoma (NFPAs) invasion and recurrence of tumor samples and the relations between quantitatively determined markers and clinical characters.
We studied 104 patients, including 59 patients without recurrence and 45 patients with recurrence (9 patients with one surgery and 36 patients operated twice, both tumors being studied). All tissues were immunostained for TGF-β1 and WIF1 using tissue microarrays and confirmed with real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) and Western blot.
We found that invasion, TGF-β1, and WIF1 were significantly associated with recurrence and that age was associated with low expression of TGF-β1 and WIF1 (P < 0.001). There were no statistically significant differences in the expression of the 2 proteins between the noninvasive and the invasive groups. The expression of TGF-β1 and WIF1 in primary tumors in the recurrence group was lower than in the nonrecurrence group (P < 0.001). In the 36 paired primary or recurrent tumors, the expression of TGF-β1 and WIF1 in recurrent tumors was higher than the expression of primary tumors, which was confirmed with qRT-PCR and Western blot. Therefore, TGF-β1 and WIF1 seem to be related to recurrence or progression of pituitary adenomas.
The expression of TGF-β1 and WIF1 in NFPAs correlated with cell proliferation and recurrence potential. They may be good markers of progressive behavior in NFPAs; however, the biologic mechanism needs further study.
本研究主要旨在研究转化生长因子β1(TGF-β1)和Wnt抑制因子1(WIF1),以预测无功能垂体腺瘤(NFPAs)肿瘤样本的侵袭和复发情况,以及定量测定的标志物与临床特征之间的关系。
我们研究了104例患者,其中包括59例无复发患者和45例复发患者(9例接受过一次手术,36例接受过两次手术,对这两次手术的肿瘤均进行研究)。使用组织芯片对所有组织进行TGF-β1和WIF1免疫染色,并通过实时定量逆转录聚合酶链反应(qRT-PCR)和蛋白质印迹法进行验证。
我们发现侵袭、TGF-β1和WIF1与复发显著相关,并且年龄与TGF-β1和WIF1的低表达相关(P<0.001)。非侵袭组和侵袭组之间这两种蛋白的表达无统计学显著差异。复发组原发性肿瘤中TGF-β1和WIF1的表达低于非复发组(P<0.