Sørensen Patricia Diana, Andersen Rikke Fredslund, Pallisgaard Niels, Madsen Jonna Skov, Jakobsen Erik Hugger, Brandslund Ivan
Department of Clinical Immunology and Biochemistry, Vejle, Lillebaelt Hospital, Denmark.
Institute of Regional Health Research, Faculty of Health Sciences, University of Southern Denmark, Odense, Denmark.
J Circ Biomark. 2015 Aug 31;4:9. doi: 10.5772/61320. eCollection 2015 Jan-Dec.
The purpose of this study was to quantify the free-circulating plasma HER-2 DNA (cfHER-2 DNA) and to assess the ability of analysis to discriminate between patients with primary breast cancer and healthy controls in order to detect metastatic recurrence in comparison with serum HER-2 protein and also HER-2 gene amplification. The study population consisted of 100 patients with primary breast cancer and 50 healthy female donors. An additional 22 patients with metastases were subsequently included. cfHER-2 DNA was quantified with a quantitative PCR method together with a reference gene.
Using a cut-off of 2.5 for the ratio of the cfHER-2 DNA/reference gene, three (of 15) tissue HER-2-positive patients had a ratio >2.5 prior to the detection of metastatic disease. In the post-metastatic/pre-chemotherapy setting, 11 (of 23) tissue HER-2-positive patients with metastases had a ratio >2.5. There was no difference between absolute preoperative cfHER-2 DNA values for patients with primary breast cancer and those for healthy controls. There was no difference between cfHER-2 DNA values taken within nine months of development of the metastatic disease and the levels in patients without metastases, but there was a significant difference in the corresponding serum HER-2 protein levels in the tissue HER-2-positive patient group.
Amplified HER-2 DNA can be detected in plasma when using a ratio between cfHER-2 DNA and a reference gene. cfHER-2 DNA could not be used to discriminate between patients with primary breast cancer and healthy controls, and could not predict the development of metastatic disease.
本研究的目的是对游离循环血浆人表皮生长因子受体2 DNA(cfHER-2 DNA)进行定量,并评估该分析方法区分原发性乳腺癌患者与健康对照的能力,以便与血清HER-2蛋白及HER-2基因扩增情况相比较来检测转移复发。研究人群包括100例原发性乳腺癌患者和50名健康女性供体。随后又纳入了22例有转移的患者。采用定量PCR方法并结合一个参照基因对cfHER-2 DNA进行定量。
对于cfHER-2 DNA/参照基因的比值,采用2.5作为临界值,15例组织HER-2阳性患者中有3例在转移疾病检测之前比值>2.5。在转移后/化疗前的情况下,23例有转移的组织HER-2阳性患者中有11例比值>2.5。原发性乳腺癌患者术前cfHER-2 DNA的绝对值与健康对照者相比没有差异。转移疾病发生后9个月内采集的cfHER-2 DNA值与无转移患者的水平之间没有差异,但在组织HER-2阳性患者组中相应的血清HER-2蛋白水平存在显著差异。
当使用cfHER-2 DNA与参照基因的比值时,可在血浆中检测到扩增的HER-2 DNA。cfHER-2 DNA不能用于区分原发性乳腺癌患者与健康对照,也不能预测转移疾病的发生。