Li Yanli, Zhang Jiarong
Department of Obstetrics and Gynecology, Affiliated First Hospital of Shanghai Jiao Tong University, Shanghai, China.
Appl Immunohistochem Mol Morphol. 2017 Feb;25(2):110-116. doi: 10.1097/PAI.0000000000000275.
S100A11 is a calcium-binding protein implicated in a variety of biological functions and is overexpressed in many human cancers. However, S100A11 expression level in ovarian cancer has not been well characterized. High-grade serous ovarian cancer (HGSC) is the most common and lethal type of ovarian cancer. The aim of the present study was to investigate S100A11 expression and its clinical significance in HGSC. S100A11 expression was evaluated by Western blot in 45 snap-frozen specimens (15 normal ovarian epithelia, 15 normal fallopian tube epithelia, and 15 HGSCs) and by immunohistochemistry in 211 paraffin-embedded specimens (40 normal fallopian tube epithelia, 54 normal ovarian epithelia, and 117 HGSCs). S100A11 expression was extremely elevated in HGSC compared with normal epithelial tissues and was positively correlated with FIGO stage (P=0.014), ascitic fluid volume (P=0.009), and residual disease (P=0.004) of HGSC patients. Higher S100A11 expression was associated with poorer disease-free (P=0.004) and overall (P=0.006) survival, whereas multivariate analysis revealed S100A11 to be an independent prognostic factor for disease-free (P=0.019) and overall (P=0.027) survival in patients with HGSC. In conclusion, S100A11 overexpression correlates with an aggressive malignant phenotype and may constitute a novel prognostic factor for HGSC.
S100A11是一种钙结合蛋白,参与多种生物学功能,且在许多人类癌症中过表达。然而,卵巢癌中S100A11的表达水平尚未得到充分表征。高级别浆液性卵巢癌(HGSC)是最常见且致死率最高的卵巢癌类型。本研究的目的是调查HGSC中S100A11的表达及其临床意义。通过蛋白质免疫印迹法评估了45份速冻标本(15份正常卵巢上皮、15份正常输卵管上皮和15份HGSC)中的S100A11表达,并通过免疫组织化学法评估了211份石蜡包埋标本(40份正常输卵管上皮、54份正常卵巢上皮和117份HGSC)中的S100A11表达。与正常上皮组织相比,HGSC中S100A11的表达极度升高,且与HGSC患者的国际妇产科联盟(FIGO)分期(P = 0.014)、腹水体积(P = 0.009)和残留病灶(P = 0.004)呈正相关。较高的S100A11表达与无病生存期(P = 0.004)和总生存期(P = 0.006)较差相关,而多变量分析显示S100A11是HGSC患者无病生存期(P = 0.019)和总生存期(P = 0.027)的独立预后因素。总之,S100A11过表达与侵袭性恶性表型相关,可能构成HGSC的一种新的预后因素。