Tian Ping, Zhang Chen, Ma Cailing, Ding Lu, Tao Ning, Ning Li, Wang Yan, Yong Xianting, Yan Qi, Lin Xin, Wang Jing, Li Rong
College of Public Health, Xinjiang Medical University, No. 393, Xinyi Road, Urumqi 830054, Xinjiang, China.
The Fifth Affiliated Hospital, Xinjiang Medical University, Urumqi 830011, Xinjiang, China.
Open Med (Wars). 2021 Mar 9;16(1):410-418. doi: 10.1515/med-2021-0015. eCollection 2021.
The aim of this study was to evaluate the association of the chromobox homologue 7 (CBX7) expression with the epithelial-mesenchymal transition in cervical cancer (CC), as well as with the disease prognosis. CBX7, E-cadherin (E-cad), and vimentin (VIM) expression levels were detected with immunohistochemistry. The relationship between the expression of CBX7, E-cad, and VIM expression and conventional clinicopathological characteristics of CC were evaluated. The positive expression rates of CBX7 and E-cad in the CC tissues were lower than the adjacent non-tumorous cervical tissues. Moreover, the VIM expression level was higher. The CBX7 expression was positively correlated with the E-cad expression, whereas was negatively correlated with the VIM expression. Furthermore, CBX7 was associated with the disease clinical staging, histological differentiation, lymph node metastasis, and vascular invasion. Patients with negative CBX7 expression showed decreased overall survival rates compared with those with low or high CBX7 expression. Multivariate Cox regression analysis indicated that the decreased CBX7 expression was an independent predictor for the poor prognosis of CC. In conclusion, the absence of CBX7 is associated with the histologic differentiation, lymphatic metastasis, vascular invasion, and poor prognosis of CC. CBX7 may be an independent prognostic factor for the prognosis of CC patients.
本研究旨在评估染色体盒同源物7(CBX7)表达与宫颈癌(CC)上皮-间质转化以及疾病预后之间的关联。采用免疫组织化学法检测CBX7、E-钙黏蛋白(E-cad)和波形蛋白(VIM)的表达水平。评估CBX7、E-cad和VIM表达与CC常规临床病理特征之间的关系。CC组织中CBX7和E-cad的阳性表达率低于相邻的非肿瘤性宫颈组织。此外,VIM表达水平较高。CBX7表达与E-cad表达呈正相关,而与VIM表达呈负相关。此外,CBX7与疾病临床分期、组织学分化、淋巴结转移和血管侵犯有关。与CBX7低表达或高表达的患者相比,CBX7表达阴性的患者总生存率降低。多因素Cox回归分析表明,CBX7表达降低是CC预后不良的独立预测因素。总之,CBX7缺失与CC的组织学分化、淋巴转移、血管侵犯和预后不良有关。CBX7可能是CC患者预后的独立预后因素。