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首页> 外文期刊>Gynecologic Oncology: An International Journal >Specificity and prognostic validation of a polyclonal antibody to detect Six1 homeoprotein in ovarian cancer
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Specificity and prognostic validation of a polyclonal antibody to detect Six1 homeoprotein in ovarian cancer

机译:检测卵巢癌中Six1同源蛋白的多克隆抗体的特异性和预后验证

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Objective: The presence of Six1 mRNA gene portends a poor prognosis in ovarian cancer. We describe validation of a Six1 specific antibody and evaluate its association with tumorigenicity and prognosis in ovarian cancer. Methods: A Six1 antibody (Six1cTerm) was raised to residues downstream of the Six1 homeodomain, representing its unique C-terminus as compared to other Six family members. Cells were transfected with Six1-Six6 and Western blot was performed to demonstrate Six1 specificity. Ovarian cancer cell lines were analyzed for Six1 mRNA and Six1cTerm and tumorigenicity was evaluated. Ovarian cancer tissue microarrays (OTMA) were analyzed for Six1cTerm by immunohistochemistry and scored by two blinded observers. The metastatic tumors of 15 stage IIIC high grade serous ovarian cancers were analyzed with Six1 mRNA and Six1cTerm and expression was compared to clinical factors and survival. Results: The Six1cTerm antibody is specific for Six1. Cell line tumorigenicity in SCID mice correlates with Six1 levels both by mRNA(p = 0.001, Mann-Whitney U test) and by protein (presence vs. absence, p = 0.05 Fischer's Exact test). Six1 protein was present in up to 54% of OTMA specimens. Six1 protein expression in omental/peritoneal metastases correlated with worsened survival in a sample (n = 15) of high grade serous stage IIIC ovarian cancers (p = 0.001). Conclusions: The Six1cTerm antibody is specific and able to detect Six1 in cell lines and tumor tissue. Six1 protein detection is common in ovarian cancer and is associated with tumorigenicity and poor prognosis in this group of patient samples. Six1cTerm antibody should be further validated as prognostic tool.
机译:目的:Six1 mRNA基因的存在预示着卵巢癌预后不良。我们描述了Six1特异性抗体的验证,并评估其与卵巢癌致瘤性和预后的关系。方法:将Six1抗体(Six1cTerm)生成到Six1同源域下游的残基,与其他六个家族成员相比,代表其唯一的C末端。用Six1-Six6转染细胞并进行蛋白质印迹以证明Six1特异性。分析卵巢癌细胞系中的Six1 mRNA和Six1cTerm,并评估其致癌性。通过免疫组织化学分析卵巢癌组织微阵列(OTMA)的Six1cTerm,并由两名盲人观察者评分。用Six1 mRNA和Six1cTerm分析15种IIIC期高级别浆液性卵巢癌的转移性肿瘤,并与临床因素和生存率进行比较。结果:Six1cTerm抗体对Six1具有特异性。通过mRNA(p = 0.001,Mann-Whitney U检验)和蛋白质(存在与否,p = 0.05 Fischer精确检验),SCID小鼠的细胞系致癌性均与Six1水平相关。在高达54%的OTMA标本中存在Six1蛋白。网膜/腹膜转移中Six1蛋白的表达与高级别浆液性IIIC期卵巢癌样本(n = 15)中生存期恶化相关(p = 0.001)。结论:Six1cTerm抗体具有特异性,能够检测细胞系和肿瘤组织中的Six1。在这组患者样本中,Six1蛋白检测在卵巢癌中很常见,并且与致癌性和不良预后有关。 Six1cTerm抗体应进一步验证为预后工具。

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