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埃及乳腺癌患者血清HER2、MMP-9、一氧化氮和总抗氧化能力水平的评估:与临床病理参数的相关性

Evaluation of Serum Levels of HER2, MMP-9, Nitric Oxide, and Total Antioxidant Capacity in Egyptian Breast Cancer Patients: Correlation with Clinico-Pathological Parameters.

作者信息

Rashad Yara A, Elkhodary Tawfik R, El-Gayar Amal M, Eissa Laila A

机构信息

Department of Biochemistry, Faculty of Pharmacy, Mansoura University, Mansoura, 35516, Egypt.

Oncology Center, Mansoura University, Mansoura, 35516, Egypt.

出版信息

Sci Pharm. 2013 Sep 22;82(1):129-45. doi: 10.3797/scipharm.1306-18. Print 2014 Jan-Mar.

DOI:10.3797/scipharm.1306-18
PMID:24634847
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3951224/
Abstract

Breast cancer is by far the most common cancer in women worldwide and the main cause of cancer-related mortality. Breast cancer accounts for 38% of all malignancies among Egyptian women. The aim of our study was to evaluate the serum levels of human epidermal growth factor receptor-2 (HER2), matrix metalloproteinase-9 (MMP-9), nitric oxide (NO), and total antioxidant capacity (TAC) in breast cancer patients and to correlate these markers with clinico-pathological parameters. Serum HER2, MMP-9, and carcinoma antigen 15-3 (CA 15-3) were assessed in 80 breast cancer patients and ten healthy subjects as a control group by the enzyme-linked immunosorbent assay (ELISA) technique while NO and TAC were assessed by a colorimetric method. Serum HER2 was ≥15 ng/mL in nine patients (11.3%). High HER2 ECD levels were significantly associated with tissue HER2 (P<0.0001), metastasis (P= 0.0024), and negativity of both estrogen (P=0.0075) and progesterone (P=0.0239) receptors. Serum MMP-9 (P=0.0013), NO (P<0.0001), and CA 15-3 (P<0.0001) were significantly increased while serum TAC was significantly (P=0.01) decreased in breast cancer patients as compared to the control group. Serum MMP-9 was increased significantly (P=0.028) in metastatic patients as compared to non-metastatic patients. We found a positive correlation between serum HER2 and CA 15-3 (r=36, p=0.005). In conclusion, serum HER2 reflects the tissue HER2 status of breast cancer, so the determination of serum HER2 is helpful in assessing HER2 status, but in addition, a high level may reflect metastatic disease. Also, serum MMP-9 can be useful for denoting the development of metastasis in breast cancer patients. Follow-up is needed to evaluate the value of serum HER2 and MMP-9 as prognostic markers.

摘要

乳腺癌是目前全球女性中最常见的癌症,也是癌症相关死亡的主要原因。乳腺癌占埃及女性所有恶性肿瘤的38%。我们研究的目的是评估乳腺癌患者血清中人表皮生长因子受体2(HER2)、基质金属蛋白酶9(MMP-9)、一氧化氮(NO)和总抗氧化能力(TAC)的水平,并将这些标志物与临床病理参数相关联。采用酶联免疫吸附测定(ELISA)技术对80例乳腺癌患者和10名健康受试者作为对照组进行血清HER2、MMP-9和癌抗原15-3(CA 15-3)评估,同时采用比色法评估NO和TAC。9例患者(11.3%)血清HER2≥15 ng/mL。HER2细胞外结构域(ECD)高水平与组织HER2(P<0.0001)、转移(P=0.0024)以及雌激素(P=0.0075)和孕激素(P=0.0239)受体阴性显著相关。与对照组相比,乳腺癌患者血清MMP-9(P=0.0013)、NO(P<0.0001)和CA 15-3(P<0.0001)显著升高,而血清TAC显著降低(P=0.01)。与非转移患者相比,转移患者血清MMP-9显著升高(P=0.028)。我们发现血清HER2与CA 15-3之间存在正相关(r=0.36,p=0.005)。总之,血清HER2反映乳腺癌的组织HER2状态,因此血清HER2的测定有助于评估HER2状态,但此外,高水平可能反映转移性疾病。此外,血清MMP-9可用于表明乳腺癌患者转移的发生。需要进行随访以评估血清HER2和MMP-9作为预后标志物的价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/3951224/c75023b97df2/scipharm.2014.82.129f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/3951224/88197f7a8a17/scipharm.2014.82.129f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/3951224/6d8373c7acf9/scipharm.2014.82.129f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/3951224/bf598e0fb9ac/scipharm.2014.82.129f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/3951224/8ae60e8e2d53/scipharm.2014.82.129f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/3951224/c75023b97df2/scipharm.2014.82.129f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/3951224/88197f7a8a17/scipharm.2014.82.129f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/3951224/fc9513193bbc/scipharm.2014.82.129f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/3951224/6d8373c7acf9/scipharm.2014.82.129f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/3951224/bf598e0fb9ac/scipharm.2014.82.129f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/3951224/8ae60e8e2d53/scipharm.2014.82.129f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f6a/3951224/c75023b97df2/scipharm.2014.82.129f6.jpg

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