Multiple biomarker panel for the detection of circulating tumor cells in peripheral blood of breast cancer patients for early detection using the real-time reverse transcription-polymerase chain reaction

被引:0
作者
Fooladi, Hanie [1 ]
Ghanbariasad, Ali [2 ,3 ]
Sepahi, Neda [2 ]
Taghinezhad, Ali [3 ]
Tahmasebi, Sedighe [4 ]
Amiri, Ahmad [5 ]
Mirzaei, Hadi [6 ]
Sahebnazar, Barasa [1 ]
机构
[1] Fasa Univ Med Sci, Fasa, Iran
[2] Fasa Univ Med Sci, Noncommunicable Dis Res Ctr, Fasa, Iran
[3] Fasa Univ Med Sci, Dept Med Biotechnol, Fasa, Iran
[4] Shiraz Univ Med Sci, Shiraz Iran Canc Res Ctr, Dept Gen Surg, Shiraz, Iran
[5] Shiraz Univ Med Sci, Med Sch, Dept Biochem, Shiraz, Iran
[6] Zabol Univ Med Sci, Sch Med, Dept Med Genet, Zabol, Iran
来源
MINERVA BIOTECHNOLOGY AND BIOMOLECULAR RESEARCH | 2021年 / 33卷 / 03期
关键词
Breast neoplasm; Real-time polymerase chain reaction; Neoplastic cells; circulating; Early diagnosis; MESSENGER-RNA MARKERS; MOLECULAR-DETECTION; HUMAN MAMMAGLOBIN; EXPRESSION; MASPIN; ASSAY; CHEMOTHERAPY; SURVIVAL; DISEASE; PREDICT;
D O I
10.23736/S2724-542X.20.02645-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
BACKGROUND: Circulating cells are epithelial cells that are detectable in the blood of breast cancer patients and the pattern of genes expression in these cells is different from that of the blood cells. However, their role in the early diagnosis of breast cancer has not yet been fully elucidated. One way of detecting these cells is through the use of molecular markers. Therefore, in this study, the presence of 5 specific genes was identified. METHODS: The expression of CK19-CK20-Maspin-Survivin-Ephb4 genes was done on 5 cell lines and peripheral blood samples from 30 breast cancer patients who had not yet entered the untreated phase using real-time polymerase chain reaction. Moreover, 30 healthy individuals were assigned to the control group. RESULTS : When only one gene was involved, the highest and lowest values of sensitivity were observed in Survivin (90%) and CK20 (40%) respectively. In addition, the highest and lowest specificity values were observed in CK 19 (90%) and Ephb4 (40%) respectively. But when the expression of all five genes was done simultaneously, the level of specificity increased to 100%, even though a sharp decrease was observed in sensitivity. CONCLUSIONS: In order to detect circulating tumor cells, evaluating the expression of a gene cannot be helpful. However, the use of biomarker panel can be very effective in detecting these types of cells and hence, the early detection of breast cancer.
引用
收藏
页码:127 / 134
页数:8
相关论文
共 50 条
  • [1] Detection of measles virus RNA on SYBR green real-time reverse transcription-polymerase chain reaction
    Ito, Masahiro
    Suga, Tomoko
    Akiyoshi, Kyoko
    Nukuzuma, Souichi
    Kon-no, Mayumi
    Umegaki, Yasuhiro
    Kohdera, Urara
    Ihara, Toshiaki
    PEDIATRICS INTERNATIONAL, 2010, 52 (04) : 611 - 615
  • [2] Simultaneous detection of parainfluenza viruses 1 and 3 by real-time reverse transcription-polymerase chain reaction
    Cordeya, Samuel
    Thomas, Yves
    Cherpillod, Pascal
    van Belle, Sandra
    Tapparel, Caroline
    Kaiser, Laurent
    JOURNAL OF VIROLOGICAL METHODS, 2009, 156 (1-2) : 166 - 168
  • [3] Detection of circulating tumor cells by reverse transcription-quantitative polymerase chain reaction and magnetic activated cell sorting in the peripheral blood of patients with hepatocellular carcinoma
    Guo, Limin
    Xu, Donghai
    Lu, Yan
    Peng, Jirun
    Jiang, Li
    MOLECULAR MEDICINE REPORTS, 2017, 16 (05) : 5894 - 5900
  • [4] Detection of a novel human coronavirus by real-time reverse-transcription polymerase chain reaction
    Corman, V. M.
    Eckerle, I.
    Bleicker, T.
    Zaki, A.
    Landt, O.
    Eschbach-Bludau, M.
    van Boheemen, S.
    Gopal, R.
    Ballhause, M.
    Bestebroer, T. M.
    Muth, D.
    Mueller, M. A.
    Drexler, J. F.
    Zambon, M.
    Osterhaus, A. D.
    Fouchier, R. M.
    Drosten, C.
    EUROSURVEILLANCE, 2012, 17 (39): : 3 - 8
  • [5] Real-time quantitative RT-PCR detection of circulating tumor cells from breast cancer patients
    Guo, Maowen
    Li, Xiaotian
    Zhang, Shaohua
    Song, Hua
    Zhang, Wenhui
    Shang, Xueyi
    Zheng, Yuling
    Jiang, Hua
    Lv, Qingyu
    Jiang, Yongqiang
    Hao, Huaijie
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2015, 46 (01) : 281 - 289
  • [6] The detection of circulating tumor cells of breast cancer patients by using multimarker (Survivin, hTERT and hMAM) quantitative real-time PCR
    Shen ChangXin
    Hu LiHua
    Xia Lin
    Li YiRong
    CLINICAL BIOCHEMISTRY, 2009, 42 (03) : 194 - 200
  • [7] Prognostic Significance of the Detection of Peripheral Blood CEACAM5mRNA-Positive Cells by Real-Time Polymerase Chain Reaction in Operable Colorectal Cancer
    Vardakis, Nikolaos
    Messaritakis, Ippokratis
    Papadaki, Chara
    Agoglossakis, Georgios
    Sfakianaki, Maria
    Saridaki, Zacharenia
    Apostolaki, Stella
    Koutroubakis, Ioannis
    Perraki, Maria
    Hatzidaki, Dora
    Mavroudis, Dimitris
    Georgoulias, Vassilis
    Souglakos, John
    CLINICAL CANCER RESEARCH, 2011, 17 (01) : 165 - 173
  • [8] Rapid detection and quantification of Ebola Zaire virus by one-step real-time quantitative reverse transcription-polymerase chain reaction
    Ro, Young-Tae
    Ticer, Anysha
    Carrion, Ricardo, Jr.
    Patterson, Jean L.
    MICROBIOLOGY AND IMMUNOLOGY, 2017, 61 (3-4) : 130 - 137
  • [9] Evaluation of the PrimerDesign™ genesig real-time reverse transcription-polymerase chain reaction assay and the INFINITI® Respiratory Viral Panel Plus assay for the detection of human metapneumovirus in Kuwait
    Al-Turab, Mariam
    Chehadeh, Wassim
    Al-Mulla, Fahd
    Al-Nakib, Widad
    DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2012, 72 (04) : 358 - 362
  • [10] Molecular Detection of Peripheral Blood Breast Cancer mRNA Transcripts as a Surrogate Biomarker for Circulating Tumor Cells
    Lasa, Adriana
    Garcia, Arnal
    Alonso, Carmen
    Millet, Pilar
    Cornet, Monica
    Ramon y Cajal, Teresa
    Baiget, Montserrat
    Barnadas, Agusti
    PLOS ONE, 2013, 8 (09):