Zhao Gang, Wang Xiaozhen, Qu Limei, Zhu Zhu, Hong Jinghui, Hou Haiqin, Li Zuonong, Wang Jun, Lv Zheng
Department of Breast Surgery, the First Affiliated Hospital of Jilin University, Changchun, China.
Department of Pathology, the First Affiliated Hospital of Jilin University, Changchun, China.
Breast Care (Basel). 2021 Feb;16(1):16-26. doi: 10.1159/000505806. Epub 2020 Mar 26.
Transcription factor SOX2 (sex-determining region Y-box 2) has a crucial role in the maintenance of the stem cell state. However, current evidence regarding the role of SOX2 in breast cancer is conflicting. We conducted this meta-analysis to clarify the association of SOX2 expression with clinical and molecular features and its prognostic effect on breast cancer.
All relevant articles were searched using electronic databases. The pooled odds ratios (ORs) or hazard ratios (HRs: multivariate Cox survival analysis) with their 95% confidence intervals (CIs) were calculated.
A final total of 18 studies containing 3,080 patients with breast cancer were included. SOX2 protein expression was not related to age, menopausal status, lymph node metastasis, lymphovascular invasion, molecular estrogen receptor status, progesterone receptor status, triple-negative status, and the overall survival in breast cancer, but was closely associated with advanced tumor grade (grade 3 vs. grade 1-2: OR = 2.74, 95% CI = 1.85-4.06, < 0.001), clinical stage (stage 3-4 vs. stage 0-2: OR = 2.46, 95% CI = 1.37-4.40, = 0.002), pT stage (T stage 2-4 vs. T stage 1: OR = 1.52, 95% CI = 1.07-2.17, = 0.019), molecular human epidermal growth factor receptor 2 (HER2) status (positive vs. negative: OR = 1.61, 95% CI = 1.21-2.14, = 0.001), epidermal growth factor receptor (EGFR) status (positive vs. negative: OR = 2.21, 95% CI = 1.13-4.33, = 0.021), and worse disease-free survival (DFS) (HR = 2.66, 95% CI = 1.20-5.91, = 0.016) of breast cancer.
SOX2 expression is correlated with breast cancer progression, HER2 status, and EGFR status, and may be an independent prognostic marker for predicting poor DFS.
转录因子SOX2(性别决定区Y框2)在维持干细胞状态中起关键作用。然而,目前关于SOX2在乳腺癌中作用的证据相互矛盾。我们进行了这项荟萃分析,以阐明SOX2表达与临床和分子特征的关联及其对乳腺癌的预后影响。
使用电子数据库检索所有相关文章。计算合并优势比(OR)或风险比(HR:多变量Cox生存分析)及其95%置信区间(CI)。
最终共纳入18项研究,包含3080例乳腺癌患者。SOX2蛋白表达与年龄、绝经状态、淋巴结转移、淋巴管浸润、分子雌激素受体状态、孕激素受体状态、三阴性状态及乳腺癌患者的总生存期无关,但与肿瘤高级别(3级vs.1 - 2级:OR = 2.74,95%CI = 1.85 - 4.06,<0.001)、临床分期(3 - 4期vs.0 - 2期:OR = 2.46,95%CI = 1.37 - 4.40,=0.002)、pT分期(T2 - 4期vs.T1期:OR = 1.52,95%CI = 1.07 - 2.17,=0.019)、分子人表皮生长因子受体2(HER2)状态(阳性vs.阴性:OR = 1.61,95%CI = 1.21 - 2.14,=0.001)、表皮生长因子受体(EGFR)状态(阳性vs.阴性:OR = 2.21,95%CI = 1.13 - 4.33,=0.021)密切相关,且与乳腺癌患者较差的无病生存期(DFS)(HR = 2.66,95%CI = 1.20 - 5.91,=0.016)相关。
SOX2表达与乳腺癌进展、HER2状态和EGFR状态相关,可能是预测DFS不良的独立预后标志物。