Zhou Yu-Ting, Qiu Juan-Juan, Wang Yao, Liu Peng-Cheng, Lv Qing, Du Zheng-Gui
West China Hospital, Sichuan University, Chengdu, China.
Front Oncol. 2019 Jul 31;9:710. doi: 10.3389/fonc.2019.00710. eCollection 2019.
The expression and role of sperm protein antigen 17 (SPA17), which has been confirmed to be immunogenic, in breast cancer remain unclear. We examined the expression of SPA17 in breast cancer and assessed its effect on patient prognosis and its function in breast cancer development. SPA17 expression was evaluated by immunohistochemistry and Q-RT-PCR in 120 breast tissue samples. Correlation of SPA17 expression with the patients' clinicopathological parameters and overall survival was assessed. The function of SPA17 was also explored. By reviewing Gene Expression Omnibus datasets, we found that SPA17 expression in ductal breast carcinoma in situ (log2[fold change] = 1.14, -value = 0.004) and invasive ductal breast cancer (log2[fold change] = 1.03, -value = 0.016) tissues was 2.20 and 2.05 times higher, respectively, than that in normal breast tissues. Our result also showed that 27% (27/100) of breast cancer samples expressed SPA17 but none of the normal breast (0/20) samples did. Lymph node metastasis ( < 0.001) and molecular subtyping ( = 0.002) were independent factors associated with SPA17 expression. Most importantly, SPA17 expression resulted in poor prognosis. In addition, cell function assay validated that SPA17 increased the migration ( < 0.001) and invasion ( = 0.007) of breast cancer cells, but not affected the proliferation of breast cancer cells. Our results demonstrated the vital role of SPA17 in the development and metastasis of breast cancer and that SPA17 may be a new therapeutic target in improving breast cancer prognosis.
精子蛋白抗原17(SPA17)已被证实具有免疫原性,但其在乳腺癌中的表达及作用尚不清楚。我们检测了SPA17在乳腺癌中的表达,评估其对患者预后的影响及其在乳腺癌发生发展中的功能。采用免疫组织化学和Q-RT-PCR方法检测了120例乳腺组织样本中SPA17的表达。评估SPA17表达与患者临床病理参数及总生存期的相关性。同时也探讨了SPA17的功能。通过查阅基因表达综合数据库,我们发现导管原位癌(log2[倍数变化]=1.14,P值=0.004)和浸润性导管癌(log2[倍数变化]=1.03,P值=0.016)组织中SPA17的表达分别比正常乳腺组织高2.20倍和2.05倍。我们的结果还显示,27%(27/100)的乳腺癌样本表达SPA17,而正常乳腺样本(0/20)均未表达。淋巴结转移(P<0.001)和分子亚型(P=0.002)是与SPA17表达相关的独立因素。最重要的是,SPA17表达导致预后不良。此外,细胞功能实验证实SPA17增加了乳腺癌细胞的迁移能力(P<0.001)和侵袭能力(P=0.007),但不影响乳腺癌细胞的增殖。我们的结果证明了SPA17在乳腺癌发生发展和转移中的重要作用,并且SPA17可能是改善乳腺癌预后的一个新的治疗靶点。