乳腺癌的免疫学和遗传学预测因子

A. Glushkov, E. Polenok, L. Gordeeva, S. Mun, E. Voronina, M. Kostyanko, A. Antonov, N. Verzhbitskaya, G. Kolpinskiy
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Prevalence of CYP1A1 (rs4646903), CYP1A2 (rs762551), CYP1B1 (rs1056836), CYP19A1 (rs2470152), GSTM1(del), GSTT1(del), and GSTP1 (rs1695) polymorphisms in 530 healthy women and 694 patients with stage 1 breast cancer were determined by real-time polymerase chain reaction.Results. Low personal IgA1 -Bp/IgA1 -Pg < 1 and IgA1 -E2/IgA1 -Pg < 1 ratios in combination with low IgG2 -E2 ≤ 4 and high IgG2 -Pg > 2 levels were found in 20.6% of healthy women and in 4.5% of breast cancer patients (p < 0.0001; OR = 0.2). Low IgA1 -Bp/IgA1 -Pg and high IgA1 -E2/IgA1 -Pg ratios in combination with low IgG2 -E2 and high IgG2 - Pg levels were revealed in 7.4% of healthy women and 2.8% of breast cancer patients (p = 0.009; OR = 0.4). These two variants were integrated and marked as protective immunological phenotype. 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引用次数: 0

摘要

的目标。目的探讨1期乳腺癌患者抗苯并[a]芘、雌二醇和黄体酮独特型IgA抗体(IgA1 - bp、IgA1 - e2和IgA1 -Pg)与相应的抗雌二醇和黄体酮独特型IgG抗体(IgG2 - e2和IgG2 -Pg)以及CYP1A1、CYP1A2、CYP1B1、CYP17A1、CYP19A1、GSTM1、GSTT1和GSTP1基因多态性的相关性。材料与方法。采用酶联免疫吸附法检测240例健康妇女和505例1期乳腺癌患者血清中独特型和抗独特型抗体。采用实时聚合酶链反应检测530例健康女性和694例1期乳腺癌患者中CYP1A1 (rs4646903)、CYP1A2 (rs762551)、CYP1B1 (rs1056836)、CYP19A1 (rs2470152)、GSTM1(del)、GSTT1(del)和GSTP1 (rs1695)多态性的流行情况。20.6%的健康女性和4.5%的乳腺癌患者存在IgA1 -Bp/IgA1 -Pg < 1和IgA1 -E2/IgA1 -Pg < 1并伴有IgG2 -E2≤4和IgG2 -Pg > 2的低个人比值(p < 0.0001;Or = 0.2)。7.4%的健康女性和2.8%的乳腺癌患者存在低IgA1 - bp /IgA1 -Pg和高IgA1 - e2 /IgA1 -Pg比值,并存在低IgG2 - e2和高IgG2 -Pg水平(p = 0.009;Or = 0.4)。这两种变异被整合并标记为保护性免疫表型。17.2%的健康女性和27.2%的乳腺癌患者存在高IgA1 - Bp/IgA1 - pg和高IgA1 - e2 /IgA1 - pg比值并伴有高IgG2 - pg和高或低IgG2 - e2水平(p = 0.006;OR = 1.8)、6.4%的健康女性和18.3%的乳腺癌患者(p < 0.0001;OR = 3.3)。这两种变异被整合并标记为致癌前免疫表型。这些关联仅在雌激素受体阳性(ER+)乳腺癌中发现。GSTP1 (rs1695)基因多态性与雌激素受体阴性(ER-)乳腺癌仅相关(p = 0.004;Or = 1.56)。CYP和GST基因的免疫表型与研究多态性之间没有相互关系。促癌免疫表型和GSTP1基因内rs1695基因多态性是ER+和ER-乳腺癌的独立预测因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunological and genetic predictors of breast cancer
Aim. To investigate the associations of idiotypic IgA antibodies against benzo[a]pyrene, estradiol and progesterone (IgA1 -Bp, IgA1 -E2, and IgA1 - Pg) with the corresponding anti-idiotypic IgG antibodies to estradiol and progesterone (IgG2 -E2 and IgG2 -Pg) and with gene polymorphisms of CYP1A1, CYP1A2, CYP1B1, CYP17A1, CYP19A1, GSTM1, GSTT1, and GSTP1 in patients with stage 1 breast cancer. Materials and Methods. Idiotypic and anti-idiotypic antibodies in the serum of 240 healthy women and 505 patients with stage 1 breast cancer were measured by enzyme-linked immunosorbent assay. Prevalence of CYP1A1 (rs4646903), CYP1A2 (rs762551), CYP1B1 (rs1056836), CYP19A1 (rs2470152), GSTM1(del), GSTT1(del), and GSTP1 (rs1695) polymorphisms in 530 healthy women and 694 patients with stage 1 breast cancer were determined by real-time polymerase chain reaction.Results. Low personal IgA1 -Bp/IgA1 -Pg < 1 and IgA1 -E2/IgA1 -Pg < 1 ratios in combination with low IgG2 -E2 ≤ 4 and high IgG2 -Pg > 2 levels were found in 20.6% of healthy women and in 4.5% of breast cancer patients (p < 0.0001; OR = 0.2). Low IgA1 -Bp/IgA1 -Pg and high IgA1 -E2/IgA1 -Pg ratios in combination with low IgG2 -E2 and high IgG2 - Pg levels were revealed in 7.4% of healthy women and 2.8% of breast cancer patients (p = 0.009; OR = 0.4). These two variants were integrated and marked as protective immunological phenotype. High IgA1 - Bp/IgA1 -Pg and high IgA1 -E2/IgA1 -Pg ratios combined with high IgG2 -Pg and high or low IgG2 -E2 levels were found in 17.2% of healthy women and27.2% of breast cancer patients (p = 0.006; OR = 1.8) and in 6.4% of healthy women and in 18.3% of breast cancer patients (p < 0.0001; OR = 3.3), correspondingly. These two variants were integrated and marked as pro-carcinogenic immunological phenotype. These associations were found only with estrogen receptor-positive (ER+) breast cancer. GSTP1 (rs1695) gene polymorphism was associated exclusively with estrogen receptor-negative (ER-) breast cancer (p = 0.004; OR = 1.56). No interrelations be tween immunological phenotypes and studied polymorphisms of CYP and GST genes have been found.Conclusion. Pro-carcinogenic immunological phenotype and rs1695 gene polymorphism within the GSTP1 gene were independent predictors of ER+ and ER- breast cancer correspondingly.
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