乳腺癌组织中苯并[a]芘、雌二醇和孕酮抗体与雌激素受体表型的关系

E. Polenok, S. Mun, L. Gordeeva, M. Kostyanko, A. Antonov, N. Verzhbitskaya, G. Kolpinskiy, A. Glushkov
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引用次数: 3

摘要

的目标。揭示针对苯并[a]芘、雌二醇和孕酮的IgA抗体(IgA- bp、IgA- es、IgA- pg)与乳腺癌进展过程中雌激素受体阳性(ER+)向雌激素受体阴性(ER-)肿瘤转化的关系。材料与方法。我们收集了338名健康志愿者和1407名乳腺癌患者的血清样本,采用酶联免疫吸附法对其进行了IgA-Bp、IgA-Es、IgA-Pg的分析。用牛血清白蛋白与Bp、Es和Pg结合物作为吸附抗原,用抗人IgA辣根过氧化物酶结合抗体检测特异性抗原结合抗体。计算个体IgA-Bp/IgA-Pg和IgA-Es/IgA-Pg比值。免疫组织化学法测定雌激素受体表型。与患有ER+(12.9%)和ER-(23.9%)肿瘤的1期乳腺癌患者相比,健康女性(43.8%)更常出现低IgA-Bp/IgA-Pg比值(≤1)和低IgA-Es/IgA-Pg比值(≤1),表明免疫保护表型。高IgA-Bp/IgA-Pg比值(>1)和高IgA-Es/IgA-Pg比值(>1)提示致癌前免疫表型的健康女性(27.5%)与ER+(65.5%)和ER-(58.7%)肿瘤的1期乳腺癌患者相比较少检出。在ER+和ER-肿瘤表型的1期乳腺癌患者中,保护性和致癌性表型的患病率差异有统计学意义(p = 0.017)。ER-肿瘤表型在II-IV期(25.6%)比1期(16.3%)更为普遍。在具有致癌前免疫表型的患者中,ER+向ER-肿瘤的转化是反映乳腺癌进展的特征(p<0.0001)。检测Bp、Es和Pg抗体可作为乳腺癌发生发展的危险标志。
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Associations of antibodies to benzo[a]pyrene, estradiol and progesterone with estrogen receptor phenotype in breast cancer tissue
Aim. To reveal the associations of IgA antibodies to benzo[a]pyrene, estradiol and progesterone (IgA-Bp, IgA-Es, IgA-Pg) with the conversion of estrogen-receptor positive (ER+) into estrogen-receptor negative (ER-) tumors during breast cancer progression.Materials and Methods. Having collected serum samples from 338 healthy volunteers and 1407 breast cancer patients, we have profiled them for IgA-Bp, IgA-Es, IgA-Pg by means of enzyme-linked immunosorbent assay. Conjugates of bovine serum albumin with Bp, Es and Pg were used as adsorbed antigens and anti-human IgA horseradish peroxidase-conjugated antibodies were used for the detection of specific antigen-bound antibodies. Individual IgA-Bp/IgA-Pg and IgA-Es/IgA-Pg ratios were calculated. Estrogen receptor phenotype was determined using immunohistochemistry.Results. Low IgA-Bp/IgA-Pg ratios (≤ 1) in combination with low IgA-Es/IgA-Pg ratios (≤ 1) indicative of protective immunophenotype were more frequently revealed in healthy women (43.8%) in comparison with stage 1 breast cancer patients with ER+ (12.9%) and ER- (23.9%) tumors. High IgA-Bp/IgA-Pg ratios (>1) with high IgA-Es/IgA-Pg ratios (>1) suggestive of pro-carcinogenic immunological phenotype were less often detected in healthy women (27.5%) as compared with stage 1 breast cancer patients with ER+ (65.5%) and ER- (58.7%) tumors. Prevalence of protective and pro-carcinogenic phenotypes significantly differed in stage 1breast cancer patients with ER+ and ER- tumor phenotypes (p = 0.017). ER- tumor phenotype was more prevalent at II-IV tumor stages (25.6%) than at the stage 1 (16.3%). Conversion of ER+ to ER- tumors reflecting the breast cancer progression was characteristic for the patients with pro-carcinogenic immunological phenotype (p<0.0001).Conclusion. Detection of antibodies against Bp, Es and Pg may be applied as a risk marker of breast cancer development and progression.
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