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采用聚合酶链反应(PCR)对循环游离DNA进行平行评估,并采用酶联免疫吸附测定(ELISA)对乳腺肿瘤中的核小体进行平行评估。

Parallel assessment of circulatory cell-free DNA by PCR and nucleosomes by ELISA in breast tumors.

作者信息

Seefeld M, El Tarhouny S, Fan A X C, Hahn S, Holzgreve W, Zhong X Y

机构信息

Laboratory for Prenatal Medicine and Gynecologic Oncology, Women's Hospital/Department of BioMedicine, University of Basel, Basel - Switzerland.

出版信息

Int J Biol Markers. 2008 Apr-Jun;23(2):69-73. doi: 10.1177/172460080802300202.

Abstract

OBJECTIVES

In order to assess the potential biomolecules for breast cancer, we analyzed in parallel the levels of cell-free glyceraldehyde 3-phosphate dehydrogenase (GAPDH) and cell-free nucleosomes in serum samples from patients with benign and malignant breast tumors. The levels of cell-free DNA obtained by quantitative PCR were compared with those obtained by enzyme-linked immunosorbent assay (ELISA).

METHODS

Twenty-three patients with benign breast tumors, 27 patients with breast cancer, and 32 age-matched healthy women were recruited. The amounts of serum nucleosomes were analyzed by ELISA and the levels of cell-free GAPDH were measured by real-time quantitative PCR. The correlation between nucleosome and cell-free GAPDH levels was examined using the Spearman rank test.

RESULTS

The levels of cell-free GAPDH were significantly higher in the serum samples of patients with benign and malignant breast tumors than in those of the control group (median 37,966 GE/mL, range 3,802-130,104 versus 11,770 GE/mL, range 2,198-73,522, p=0.035 and median 40,698 GE/mL, range 3,644-192,482 versus 11,770 GE/mL range 2,198-73,522, p=0.001). The concentration of cell-free GAPDH correlated significantly with the quantities of nucleosomes in serum samples (r=0.451, p=0.000). There was, however, no significant difference between healthy individuals and women with benign breast tumors or breast cancer in terms of nucleosomes determined by ELISA.

CONCLUSION

Our data suggest that the cell-free serum GAPDH DNA assayed by quantitative PCR is a better biomarker than nucleosomes assayed by ELISA in patients with breast tumors.

摘要

目的

为了评估乳腺癌潜在的生物分子,我们同时分析了患有良性和恶性乳腺肿瘤患者血清样本中无细胞甘油醛-3-磷酸脱氢酶(GAPDH)和无细胞核小体的水平。通过定量PCR获得的无细胞DNA水平与通过酶联免疫吸附测定(ELISA)获得的水平进行了比较。

方法

招募了23名患有良性乳腺肿瘤的患者、27名患有乳腺癌的患者以及32名年龄匹配的健康女性。通过ELISA分析血清核小体的量,通过实时定量PCR测量无细胞GAPDH的水平。使用Spearman秩检验检查核小体与无细胞GAPDH水平之间的相关性。

结果

患有良性和恶性乳腺肿瘤患者的血清样本中无细胞GAPDH水平显著高于对照组(中位数37,966 GE/mL,范围3,802 - 130,104,而对照组为11,770 GE/mL,范围2,198 - 73,522,p = 0.035;中位数40,698 GE/mL,范围3,644 - 192,482,而对照组为11,770 GE/mL,范围2,198 - 73,522,p = 0.001)。血清样本中无细胞GAPDH的浓度与核小体的量显著相关(r = 0.451,p = 0.000)。然而,通过ELISA测定的核小体在健康个体与患有良性乳腺肿瘤或乳腺癌的女性之间没有显著差异。

结论

我们的数据表明,在乳腺肿瘤患者中,通过定量PCR测定的无细胞血清GAPDH DNA是比通过ELISA测定的核小体更好的生物标志物。

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