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Published in: International Journal of Clinical Oncology 5/2015

01-10-2015 | Original Article

Detection of circulating tumor cell-specific markers in breast cancer patients using the quantitative RT-PCR assay

Authors: Hye-young Wang, Sungwoo Ahn, Sunghyun Kim, Sunyoung Park, Dongju Jung, Sangjung Park, Hyunju Han, JooHyuk Sohn, SeungIl Kim, Hyeyoung Lee

Published in: International Journal of Clinical Oncology | Issue 5/2015

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Abstract

Background

Breast cancer is a highly prevalent disease among women worldwide. While the expression of certain proteins within breast cancer tumors is used to determine the prognosis and select therapies, additional markers need to be identified. Circulating tumor cells (CTCs) are constituent cells that have detached from a primary tumor to circulate in the bloodstream. CTCs are considered the main source of breast cancer metastases; therefore, detection of CTCs could be a promising diagnostic method for metastatic breast cancer.

Methods

In this study, the CircleGen CTC RT-qDx assay was used to analyze the mRNA expression levels of six CTC-specific markers including EpCAM, CK19, HER2, Ki67, hTERT, and vimentin with a total of 692 peripheral whole blood samples from 221 breast cancer patients and 376 healthy individuals.

Results

This assay showed high specificity with multiple markers; none of the healthy controls were detected positive, whereas 21.7 and 14 % of breast cancer patients were positive for EpCAM and CK19, respectively. Of the 221 breast cancer patients, 84 (38 %), 46 (20.8 %), 83 (37.6 %), and 39 (17.6 %) were positively for HER2, Ki67, hTERT, and vimentin mRNA, respectively. Of the 84 patients who were HER2 positive, nine (4 %) were also positive for EpCAM, CK19, Ki67, hTERT, and vimentin. Of the 139 breast cancer patients who were HER2 negative, 65 (29.1 %) were negative for EpCAM, CK19, Ki67, hTERT, and vimentin. Furthermore, the EpCAM-positive population decreased from 21.5 to 8.3 % after completion of anti-tumor treatment (TP4). Similarly, the CK19, HER2, hTERT, and vimentin positives also decreased from 13.9 to 9.5 %, from 37.7 to 21.4 %, from 37.2 to 33.3 %, and from 17.5 to 14.3 %, respectively, after completion of anti-tumor treatment. In contrast, the Ki67 positives increased from 20.6 to 41.7 % after completion of anti-tumor treatment.

Conclusions

mRNA overexpression of six CTC-specific markers was detected by the CircleGen CTC RT-qDx assay with high specificity, and the obtained mRNA expression levels of CTC-specific markers might provide useful criteria to select appropriate anti-tumor treatment for breast cancer patients.
Literature
1.
go back to reference Coughlin SS, Ekwueme DU (2009) Breast cancer as a global health concern. Cancer Epidemiol 33:315–318CrossRefPubMed Coughlin SS, Ekwueme DU (2009) Breast cancer as a global health concern. Cancer Epidemiol 33:315–318CrossRefPubMed
3.
go back to reference Ignatiadis M, Georgoulias V, Mavroudis D (2008) Micrometastatic disease in breast cancer: clinical implications. Eur J Cancer 44:2726–2736CrossRefPubMed Ignatiadis M, Georgoulias V, Mavroudis D (2008) Micrometastatic disease in breast cancer: clinical implications. Eur J Cancer 44:2726–2736CrossRefPubMed
4.
go back to reference Slade MJ, Coombes RC (2007) The clinical significance of disseminated tumor cells in breast cancer. Nat Clin Pract Oncol 4:30–41CrossRefPubMed Slade MJ, Coombes RC (2007) The clinical significance of disseminated tumor cells in breast cancer. Nat Clin Pract Oncol 4:30–41CrossRefPubMed
5.
go back to reference Alunni-Fabbroni M, Sandri MT (2010) Circulating tumour cells in clinical practice: Methods of detection and possible characterization. Methods 50:289–297CrossRefPubMed Alunni-Fabbroni M, Sandri MT (2010) Circulating tumour cells in clinical practice: Methods of detection and possible characterization. Methods 50:289–297CrossRefPubMed
6.
go back to reference Ignatiadis M, Georgoulias V, Mavroudis D (2008) Circulating tumor cells in breast cancer. Curr Opin Obstet Gynecol 20:55–60CrossRefPubMed Ignatiadis M, Georgoulias V, Mavroudis D (2008) Circulating tumor cells in breast cancer. Curr Opin Obstet Gynecol 20:55–60CrossRefPubMed
7.
go back to reference Parikh RR, Yang Q, Higgins SA et al (2008) Outcomes in young women with breast cancer of triple-negative phenotype: the prognostic significance of CK19 expression. Int J Radiat Oncol Biol Phys 70:35–42CrossRefPubMed Parikh RR, Yang Q, Higgins SA et al (2008) Outcomes in young women with breast cancer of triple-negative phenotype: the prognostic significance of CK19 expression. Int J Radiat Oncol Biol Phys 70:35–42CrossRefPubMed
8.
go back to reference Elder EE, Xu D, Höög A et al (2003) KI-67 AND hTERT expression can aid in the distinction between malignant and benign pheochromocytoma and paraganglioma. Mod Pathol 16:246–255CrossRefPubMed Elder EE, Xu D, Höög A et al (2003) KI-67 AND hTERT expression can aid in the distinction between malignant and benign pheochromocytoma and paraganglioma. Mod Pathol 16:246–255CrossRefPubMed
9.
go back to reference Domagala W, Lasota J, Dukowicz A et al (1990) Vimentin expression appears to be associated with poor prognosis in node-negative ductal NOS breast carcinomas. Am J Pathol 137:1299–1304PubMedCentralPubMed Domagala W, Lasota J, Dukowicz A et al (1990) Vimentin expression appears to be associated with poor prognosis in node-negative ductal NOS breast carcinomas. Am J Pathol 137:1299–1304PubMedCentralPubMed
10.
go back to reference Radhika K, Prayaga AK (2010) Estrogen and progesterone hormone receptor status in breast carcinoma: comparison of immunocytochemistry and immunohistochemistry. Indian J Cancer 47:148–150CrossRefPubMed Radhika K, Prayaga AK (2010) Estrogen and progesterone hormone receptor status in breast carcinoma: comparison of immunocytochemistry and immunohistochemistry. Indian J Cancer 47:148–150CrossRefPubMed
11.
go back to reference Moretti E, Desmedt C, Biagioni C et al (2013) TOP2A protein by quantitative immunofluorescence as a predictor of response to epirubicin in the neoadjuvant treatment of breast cancer. Future Oncol 9:1477–1487CrossRefPubMed Moretti E, Desmedt C, Biagioni C et al (2013) TOP2A protein by quantitative immunofluorescence as a predictor of response to epirubicin in the neoadjuvant treatment of breast cancer. Future Oncol 9:1477–1487CrossRefPubMed
12.
go back to reference Swennenhuis JF, Reumers J, Thys K et al (2013) Efficiency of whole genome amplification of single circulating tumor cells enriched by Cell Search and sorted by FACS. Genome Med 5:106PubMedCentralCrossRefPubMed Swennenhuis JF, Reumers J, Thys K et al (2013) Efficiency of whole genome amplification of single circulating tumor cells enriched by Cell Search and sorted by FACS. Genome Med 5:106PubMedCentralCrossRefPubMed
13.
go back to reference Van der Auwera I, Peeters D, Benoy IH et al (2010) Circulating tumour cell detection: a direct comparison between the Cell Search System, the Adna test and CK-19/mammaglobin RT-PCR in patients with metastatic breast cancer. Br J Cancer 102:276–284PubMedCentralCrossRefPubMed Van der Auwera I, Peeters D, Benoy IH et al (2010) Circulating tumour cell detection: a direct comparison between the Cell Search System, the Adna test and CK-19/mammaglobin RT-PCR in patients with metastatic breast cancer. Br J Cancer 102:276–284PubMedCentralCrossRefPubMed
14.
go back to reference Raimondi C, Gradilone A, Naso G et al (2014) Clinical utility of circulating tumor cell counting through Cell Search(®): the dilemma of a concept suspended in Limbo. Onco Targets Ther 7:619–625PubMedCentralPubMed Raimondi C, Gradilone A, Naso G et al (2014) Clinical utility of circulating tumor cell counting through Cell Search(®): the dilemma of a concept suspended in Limbo. Onco Targets Ther 7:619–625PubMedCentralPubMed
15.
go back to reference Müller V, Riethdorf S, Rack B et al (2012) Prognostic impact of circulating tumor cells assessed with the Cell Search System™ and Adna Test Breast™ in metastatic breast cancer patients: the detect study. Breast Cancer Res 14:R118PubMedCentralCrossRefPubMed Müller V, Riethdorf S, Rack B et al (2012) Prognostic impact of circulating tumor cells assessed with the Cell Search System™ and Adna Test Breast™ in metastatic breast cancer patients: the detect study. Breast Cancer Res 14:R118PubMedCentralCrossRefPubMed
16.
go back to reference Andreopoulou E, Yang LY, Rangel KM et al (2012) Comparison of assay methods for detection of circulating tumor cells in metastatic breast cancer: AdnaGen Adna Test Breast Cancer Select/Detect™ versus Veridex Cell Search™ system. Int J Cancer 130:1590–1597CrossRefPubMed Andreopoulou E, Yang LY, Rangel KM et al (2012) Comparison of assay methods for detection of circulating tumor cells in metastatic breast cancer: AdnaGen Adna Test Breast Cancer Select/Detect™ versus Veridex Cell Search™ system. Int J Cancer 130:1590–1597CrossRefPubMed
17.
go back to reference Amadori A, Rossi E, Zamarchi R et al (2009) Circulating and disseminated tumor cells in the clinical management of breast cancer patients: unanswered questions. Oncology 76:375–386CrossRefPubMed Amadori A, Rossi E, Zamarchi R et al (2009) Circulating and disseminated tumor cells in the clinical management of breast cancer patients: unanswered questions. Oncology 76:375–386CrossRefPubMed
18.
go back to reference Wang HY, Ahn S, Kim S et al (2014) Detection of circulating tumor cells in patients with breast cancer using the quantitative RT-PCR assay for monitoring of therapy efficacy. Exp Mol Pathol 97:445–452CrossRefPubMed Wang HY, Ahn S, Kim S et al (2014) Detection of circulating tumor cells in patients with breast cancer using the quantitative RT-PCR assay for monitoring of therapy efficacy. Exp Mol Pathol 97:445–452CrossRefPubMed
20.
go back to reference Riethdorf S, Fritsche H, Müller V et al (2007) Detection of circulating tumor cells in peripheral blood of patients with metastatic breast cancer: a validation study of the cell search system. Clin Cancer Res 13:920–928CrossRefPubMed Riethdorf S, Fritsche H, Müller V et al (2007) Detection of circulating tumor cells in peripheral blood of patients with metastatic breast cancer: a validation study of the cell search system. Clin Cancer Res 13:920–928CrossRefPubMed
21.
go back to reference Ntoulia M, Kaklamanis L, Valavanis C et al (2006) HER-2 DNA quantification of paraffin-embedded breast carcinomas with Light Cycler real-time PCR in comparison to immunohistochemistry and chromogenic in situ hybridization. Clin Biochem 39:942–946CrossRefPubMed Ntoulia M, Kaklamanis L, Valavanis C et al (2006) HER-2 DNA quantification of paraffin-embedded breast carcinomas with Light Cycler real-time PCR in comparison to immunohistochemistry and chromogenic in situ hybridization. Clin Biochem 39:942–946CrossRefPubMed
22.
go back to reference Fehm T, Müller V, Aktas B et al (2010) HER2 status of circulating tumor cells in patients with metastatic breast cancer: a prospective, multicenter trial. Breast Cancer Res Treat 124:403–412CrossRefPubMed Fehm T, Müller V, Aktas B et al (2010) HER2 status of circulating tumor cells in patients with metastatic breast cancer: a prospective, multicenter trial. Breast Cancer Res Treat 124:403–412CrossRefPubMed
23.
go back to reference Maestro LM, Sastre J, Rafael SB et al (2009) Circulating tumor cells in solid tumor in metastatic and localized stages. Anticancer Res 29:4839–4843PubMed Maestro LM, Sastre J, Rafael SB et al (2009) Circulating tumor cells in solid tumor in metastatic and localized stages. Anticancer Res 29:4839–4843PubMed
24.
Metadata
Title
Detection of circulating tumor cell-specific markers in breast cancer patients using the quantitative RT-PCR assay
Authors
Hye-young Wang
Sungwoo Ahn
Sunghyun Kim
Sunyoung Park
Dongju Jung
Sangjung Park
Hyunju Han
JooHyuk Sohn
SeungIl Kim
Hyeyoung Lee
Publication date
01-10-2015
Publisher
Springer Japan
Published in
International Journal of Clinical Oncology / Issue 5/2015
Print ISSN: 1341-9625
Electronic ISSN: 1437-7772
DOI
https://doi.org/10.1007/s10147-015-0798-3

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