Free Circulating Tumor DNA as a Diagnostic Marker for Breast Cancer

Background Cell‐free DNA (cfDNA) in the plasma of patients with both malignant and benign breast lesions was analyzed to determine whether the findings may have diagnostic and prognostic implications and to analyze the association between the levels of cfDNA and prognostic parameters. Methods Plasma...

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Published inJournal of clinical laboratory analysis Vol. 26; no. 6; pp. 467 - 472
Main Authors Hashad, D., Sorour, A., Ghazal, A., Talaat, I.
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.11.2012
John Wiley & Sons, Inc
John Wiley and Sons Inc
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ISSN0887-8013
1098-2825
1098-2825
DOI10.1002/jcla.21548

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Abstract Background Cell‐free DNA (cfDNA) in the plasma of patients with both malignant and benign breast lesions was analyzed to determine whether the findings may have diagnostic and prognostic implications and to analyze the association between the levels of cfDNA and prognostic parameters. Methods Plasma samples were obtained from 99 subjects; 42 with breast cancer (BC), 30 with benign breast lesions, and 27 healthy women as normal controls. Circulatory cfDNA was extracted from the plasma samples and quantified using a real‐time quantitative PCR method. Immunohistochemistry was done on formalin‐fixed paraffin‐embedded sections to evaluate the status of hormonal receptors (estrogen receptor [ER] and progesterone receptor [PR]), and the protein expression of both Her2/neu and Topoisomerase IIα. Results The level of cfDNA in the BC group was significantly higher than in the benign lesions and control groups. cfDNA level was associated with malignant tumor size, lymph node involvement, stage, and grade as well as Her2/neu and Topoisomerase IIα expression, while it was not associated with ER or PR status. Conclusions The present study suggests that the level of cfDNA can be easily quantified using plasma samples. Thus, level of plasma cfDNA might constitute an important noninvasive diagnostic and prognostic valuable tool in cancer breast patients’ management.
AbstractList Background Cell-free DNA (cf DNA ) in the plasma of patients with both malignant and benign breast lesions was analyzed to determine whether the findings may have diagnostic and prognostic implications and to analyze the association between the levels of cf DNA and prognostic parameters. Methods Plasma samples were obtained from 99 subjects; 42 with breast cancer (BC), 30 with benign breast lesions, and 27 healthy women as normal controls. Circulatory cf DNA was extracted from the plasma samples and quantified using a real-time quantitative PCR method. Immunohistochemistry was done on formalin-fixed paraffin-embedded sections to evaluate the status of hormonal receptors (estrogen receptor [ER] and progesterone receptor [PR]), and the protein expression of both Her2/neu and Topoisomerase II[alpha]. Results The level of cf DNA in the BC group was significantly higher than in the benign lesions and control groups. cf DNA level was associated with malignant tumor size, lymph node involvement, stage, and grade as well as Her2/neu and Topoisomerase II[alpha] expression, while it was not associated with ER or PR status. Conclusions The present study suggests that the level of cf DNA can be easily quantified using plasma samples. Thus, level of plasma cf DNA might constitute an important noninvasive diagnostic and prognostic valuable tool in cancer breast patients' management.
Background Cell-free DNA (cfDNA) in the plasma of patients with both malignant and benign breast lesions was analyzed to determine whether the findings may have diagnostic and prognostic implications and to analyze the association between the levels of cfDNA and prognostic parameters. Methods Plasma samples were obtained from 99 subjects; 42 with breast cancer (BC), 30 with benign breast lesions, and 27 healthy women as normal controls. Circulatory cfDNA was extracted from the plasma samples and quantified using a real-time quantitative PCR method. Immunohistochemistry was done on formalin-fixed paraffin-embedded sections to evaluate the status of hormonal receptors (estrogen receptor [ER] and progesterone receptor [PR]), and the protein expression of both Her2/neu and Topoisomerase II[alpha]. Results The level of cfDNA in the BC group was significantly higher than in the benign lesions and control groups. cfDNA level was associated with malignant tumor size, lymph node involvement, stage, and grade as well as Her2/neu and Topoisomerase II[alpha] expression, while it was not associated with ER or PR status. Conclusions The present study suggests that the level of cfDNA can be easily quantified using plasma samples. Thus, level of plasma cfDNA might constitute an important noninvasive diagnostic and prognostic valuable tool in cancer breast patients' management. [PUBLICATION ABSTRACT]
Background Cell‐free DNA (cfDNA) in the plasma of patients with both malignant and benign breast lesions was analyzed to determine whether the findings may have diagnostic and prognostic implications and to analyze the association between the levels of cfDNA and prognostic parameters. Methods Plasma samples were obtained from 99 subjects; 42 with breast cancer (BC), 30 with benign breast lesions, and 27 healthy women as normal controls. Circulatory cfDNA was extracted from the plasma samples and quantified using a real‐time quantitative PCR method. Immunohistochemistry was done on formalin‐fixed paraffin‐embedded sections to evaluate the status of hormonal receptors (estrogen receptor [ER] and progesterone receptor [PR]), and the protein expression of both Her2/neu and Topoisomerase IIα. Results The level of cfDNA in the BC group was significantly higher than in the benign lesions and control groups. cfDNA level was associated with malignant tumor size, lymph node involvement, stage, and grade as well as Her2/neu and Topoisomerase IIα expression, while it was not associated with ER or PR status. Conclusions The present study suggests that the level of cfDNA can be easily quantified using plasma samples. Thus, level of plasma cfDNA might constitute an important noninvasive diagnostic and prognostic valuable tool in cancer breast patients’ management.
Cell-free DNA (cfDNA) in the plasma of patients with both malignant and benign breast lesions was analyzed to determine whether the findings may have diagnostic and prognostic implications and to analyze the association between the levels of cfDNA and prognostic parameters.BACKGROUNDCell-free DNA (cfDNA) in the plasma of patients with both malignant and benign breast lesions was analyzed to determine whether the findings may have diagnostic and prognostic implications and to analyze the association between the levels of cfDNA and prognostic parameters.Plasma samples were obtained from 99 subjects; 42 with breast cancer (BC), 30 with benign breast lesions, and 27 healthy women as normal controls. Circulatory cfDNA was extracted from the plasma samples and quantified using a real-time quantitative PCR method. Immunohistochemistry was done on formalin-fixed paraffin-embedded sections to evaluate the status of hormonal receptors (estrogen receptor [ER] and progesterone receptor [PR]), and the protein expression of both Her2/neu and Topoisomerase IIα.METHODSPlasma samples were obtained from 99 subjects; 42 with breast cancer (BC), 30 with benign breast lesions, and 27 healthy women as normal controls. Circulatory cfDNA was extracted from the plasma samples and quantified using a real-time quantitative PCR method. Immunohistochemistry was done on formalin-fixed paraffin-embedded sections to evaluate the status of hormonal receptors (estrogen receptor [ER] and progesterone receptor [PR]), and the protein expression of both Her2/neu and Topoisomerase IIα.The level of cfDNA in the BC group was significantly higher than in the benign lesions and control groups. cfDNA level was associated with malignant tumor size, lymph node involvement, stage, and grade as well as Her2/neu and Topoisomerase IIα expression, while it was not associated with ER or PR status.RESULTSThe level of cfDNA in the BC group was significantly higher than in the benign lesions and control groups. cfDNA level was associated with malignant tumor size, lymph node involvement, stage, and grade as well as Her2/neu and Topoisomerase IIα expression, while it was not associated with ER or PR status.The present study suggests that the level of cfDNA can be easily quantified using plasma samples. Thus, level of plasma cfDNA might constitute an important noninvasive diagnostic and prognostic valuable tool in cancer breast patients' management.CONCLUSIONSThe present study suggests that the level of cfDNA can be easily quantified using plasma samples. Thus, level of plasma cfDNA might constitute an important noninvasive diagnostic and prognostic valuable tool in cancer breast patients' management.
Cell-free DNA (cfDNA) in the plasma of patients with both malignant and benign breast lesions was analyzed to determine whether the findings may have diagnostic and prognostic implications and to analyze the association between the levels of cfDNA and prognostic parameters. Plasma samples were obtained from 99 subjects; 42 with breast cancer (BC), 30 with benign breast lesions, and 27 healthy women as normal controls. Circulatory cfDNA was extracted from the plasma samples and quantified using a real-time quantitative PCR method. Immunohistochemistry was done on formalin-fixed paraffin-embedded sections to evaluate the status of hormonal receptors (estrogen receptor [ER] and progesterone receptor [PR]), and the protein expression of both Her2/neu and Topoisomerase IIα. The level of cfDNA in the BC group was significantly higher than in the benign lesions and control groups. cfDNA level was associated with malignant tumor size, lymph node involvement, stage, and grade as well as Her2/neu and Topoisomerase IIα expression, while it was not associated with ER or PR status. The present study suggests that the level of cfDNA can be easily quantified using plasma samples. Thus, level of plasma cfDNA might constitute an important noninvasive diagnostic and prognostic valuable tool in cancer breast patients' management.
Author Sorour, A.
Talaat, I.
Ghazal, A.
Hashad, D.
AuthorAffiliation 3 Pathology Department Faculty of Medicine Alexandria University Alexandria Egypt
1 Clinical Pathology Department Faculty of Medicine Alexandria University Alexandria Egypt
2 General Surgery Department Faculty of Medicine Alexandria University Alexandria Egypt
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Snippet Background Cell‐free DNA (cfDNA) in the plasma of patients with both malignant and benign breast lesions was analyzed to determine whether the findings may...
Cell-free DNA (cfDNA) in the plasma of patients with both malignant and benign breast lesions was analyzed to determine whether the findings may have...
Background Cell-free DNA (cfDNA) in the plasma of patients with both malignant and benign breast lesions was analyzed to determine whether the findings may...
Background Cell-free DNA (cf DNA ) in the plasma of patients with both malignant and benign breast lesions was analyzed to determine whether the findings may...
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pubmed
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SourceType Open Access Repository
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StartPage 467
SubjectTerms Antigens, Neoplasm - biosynthesis
Benign
Biomarkers, Tumor - blood
Breast cancer
Breast Neoplasms - blood
Breast Neoplasms - diagnosis
Breast Neoplasms - pathology
Case-Control Studies
cell free plasma DNA
Deoxyribonucleic acid
Diagnostic tests
DNA
DNA Topoisomerases, Type II - biosynthesis
DNA, Neoplasm - blood
DNA-Binding Proteins - biosynthesis
Female
Humans
Neoplasm Staging
Plasma
Real-Time Polymerase Chain Reaction
real-time quantitative PCR
Receptor, ErbB-2 - biosynthesis
Receptors, Estrogen - biosynthesis
Receptors, Progesterone - biosynthesis
Title Free Circulating Tumor DNA as a Diagnostic Marker for Breast Cancer
URI https://api.istex.fr/ark:/67375/WNG-GK4XPF0H-7/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjcla.21548
https://www.ncbi.nlm.nih.gov/pubmed/23143630
https://www.proquest.com/docview/1436247166
https://www.proquest.com/docview/1151701246
https://www.proquest.com/docview/1448224360
https://pubmed.ncbi.nlm.nih.gov/PMC6807470
Volume 26
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