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Reduced Serum Circulation of Cell-Free DNA Following Chemotherapy in Breast Cancer Patients
Breast cancer is the most common malignancy in women, with alarming mortalities. Neoadjuvant treatments employ chemotherapy to shrink tumours to a well-defined size for a better surgical outcome. The current means of assessing effectiveness of chemotherapy management are imprecise. We previously sho...
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Published in: | Medical sciences (Basel) 2021-05, Vol.9 (2), p.37 |
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creator | Adusei, Evelyn Ahenkorah, John Adu-Aryee, Nii Armah Adutwum-Ofosu, Kevin Kofi Tagoe, Emmanuel Ayitey Koney, Nii Koney-Kwaku Nkansah, Emmanuel Aryee, Nii Ayite Blay, Richard Michael Hottor, Bismarck Afedo Clegg-Lamptey, Joe-Nat Arko-Boham, Benjamin |
description | Breast cancer is the most common malignancy in women, with alarming mortalities. Neoadjuvant treatments employ chemotherapy to shrink tumours to a well-defined size for a better surgical outcome. The current means of assessing effectiveness of chemotherapy management are imprecise. We previously showed that breast cancer patients have higher serum circulating cell-free DNA concentrations. cfDNA is degraded cellular DNA fragments released into the bloodstream. We further report on the utility of cfDNA in assessing the response to chemotherapy and its potential as a monitoring biomarker. A total of 32 newly diagnosed and treatment-naive female breast cancer patients and 32 healthy females as controls were included. Anthropometric, demographic and clinicopathological information of participants were recorded. Each participant donated 5 mL of venous blood from which sera were separated. Blood sampling was carried out before the commencement of chemotherapy (timepoint 1) and after the third cycle of chemotherapy (timepoint 2). qPCR was performed on the sera to quantify ALU 115 and 247 levels, and DNA integrity (ALU247/ALU115) was determined. ALU 115 and 247 levels were elevated in cancer patients but were significantly decreased after the third cycle of chemotherapy (T2) compared to T1. DNA integrity increased after the third cycle. Serum cfDNA may provide a relatively inexpensive and minimally invasive procedure to evaluate the response to chemotherapy in breast cancer. |
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Neoadjuvant treatments employ chemotherapy to shrink tumours to a well-defined size for a better surgical outcome. The current means of assessing effectiveness of chemotherapy management are imprecise. We previously showed that breast cancer patients have higher serum circulating cell-free DNA concentrations. cfDNA is degraded cellular DNA fragments released into the bloodstream. We further report on the utility of cfDNA in assessing the response to chemotherapy and its potential as a monitoring biomarker. A total of 32 newly diagnosed and treatment-naive female breast cancer patients and 32 healthy females as controls were included. Anthropometric, demographic and clinicopathological information of participants were recorded. Each participant donated 5 mL of venous blood from which sera were separated. Blood sampling was carried out before the commencement of chemotherapy (timepoint 1) and after the third cycle of chemotherapy (timepoint 2). qPCR was performed on the sera to quantify ALU 115 and 247 levels, and DNA integrity (ALU247/ALU115) was determined. ALU 115 and 247 levels were elevated in cancer patients but were significantly decreased after the third cycle of chemotherapy (T2) compared to T1. DNA integrity increased after the third cycle. Serum cfDNA may provide a relatively inexpensive and minimally invasive procedure to evaluate the response to chemotherapy in breast cancer.</description><identifier>ISSN: 2076-3271</identifier><identifier>EISSN: 2076-3271</identifier><identifier>DOI: 10.3390/medsci9020037</identifier><identifier>PMID: 34070520</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Apoptosis ; biomarker ; Biomarkers, Tumor - genetics ; Breast cancer ; Breast Neoplasms - drug therapy ; Cancer therapies ; Cell-Free Nucleic Acids ; cfDNA ; Chemotherapy ; circulating cell-free DNA ; DNA ; Drugs ; Female ; Genomes ; Health care ; Hospitals ; Humans ; Metastasis ; Mortality ; Neoadjuvant Therapy ; RNA polymerase</subject><ispartof>Medical sciences (Basel), 2021-05, Vol.9 (2), p.37</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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Neoadjuvant treatments employ chemotherapy to shrink tumours to a well-defined size for a better surgical outcome. The current means of assessing effectiveness of chemotherapy management are imprecise. We previously showed that breast cancer patients have higher serum circulating cell-free DNA concentrations. cfDNA is degraded cellular DNA fragments released into the bloodstream. We further report on the utility of cfDNA in assessing the response to chemotherapy and its potential as a monitoring biomarker. A total of 32 newly diagnosed and treatment-naive female breast cancer patients and 32 healthy females as controls were included. Anthropometric, demographic and clinicopathological information of participants were recorded. Each participant donated 5 mL of venous blood from which sera were separated. Blood sampling was carried out before the commencement of chemotherapy (timepoint 1) and after the third cycle of chemotherapy (timepoint 2). qPCR was performed on the sera to quantify ALU 115 and 247 levels, and DNA integrity (ALU247/ALU115) was determined. ALU 115 and 247 levels were elevated in cancer patients but were significantly decreased after the third cycle of chemotherapy (T2) compared to T1. DNA integrity increased after the third cycle. Serum cfDNA may provide a relatively inexpensive and minimally invasive procedure to evaluate the response to chemotherapy in breast cancer.</description><subject>Apoptosis</subject><subject>biomarker</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Cancer therapies</subject><subject>Cell-Free Nucleic Acids</subject><subject>cfDNA</subject><subject>Chemotherapy</subject><subject>circulating cell-free DNA</subject><subject>DNA</subject><subject>Drugs</subject><subject>Female</subject><subject>Genomes</subject><subject>Health care</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Metastasis</subject><subject>Mortality</subject><subject>Neoadjuvant Therapy</subject><subject>RNA polymerase</subject><issn>2076-3271</issn><issn>2076-3271</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkk1v1DAQhiMEolXpkSuyxIVLYOxx4viCVAILlSpAfJw4WI4z2fUqG2_tBNR_j2FL1cUXW_bjR57XUxRPObxE1PBqR31yXoMAQPWgOBWg6hKF4g_vrU-K85S2kIfm2FTwuDhBCQoqAafFjy_UL4569pXismOtj24Z7ezDxMLAWhrHchWJ2NuPF2wVxjH88tOatRvahXlD0e5vmJ_Ym0g2zay1k6PIPuf7NM3pSfFosGOi89v5rPi-evet_VBefXp_2V5clQ51rcpea5BS215DX4HiUJOzHQ4EHa8kSHBSoNTKkegawKFqUHJllRoUDKAJz4rLg7cPdmv20e9svDHBevN3I8S1sXH2biTTDEJA0yOh7GQHunFaEhdka9QVaJ1drw-u_dLldF2uI9rxSHp8MvmNWYefpuE1AocseHEriOF6oTSbnU8u52gnCksyosJaKs4lZvT5f-g2LHHKUWVKykpwVCJT5YFyMaQUabh7DAfzpwvMURdk_tn9Cu7of3-OvwEP26u6</recordid><startdate>20210525</startdate><enddate>20210525</enddate><creator>Adusei, Evelyn</creator><creator>Ahenkorah, John</creator><creator>Adu-Aryee, Nii Armah</creator><creator>Adutwum-Ofosu, Kevin Kofi</creator><creator>Tagoe, Emmanuel Ayitey</creator><creator>Koney, Nii Koney-Kwaku</creator><creator>Nkansah, Emmanuel</creator><creator>Aryee, Nii Ayite</creator><creator>Blay, Richard Michael</creator><creator>Hottor, Bismarck Afedo</creator><creator>Clegg-Lamptey, Joe-Nat</creator><creator>Arko-Boham, Benjamin</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-0497-071X</orcidid><orcidid>https://orcid.org/0000-0002-0617-5210</orcidid><orcidid>https://orcid.org/0000-0001-6429-2186</orcidid><orcidid>https://orcid.org/0000-0001-7179-1872</orcidid><orcidid>https://orcid.org/0000-0002-5356-4323</orcidid><orcidid>https://orcid.org/0000-0002-3731-3399</orcidid><orcidid>https://orcid.org/0000-0002-0286-473X</orcidid></search><sort><creationdate>20210525</creationdate><title>Reduced Serum Circulation of Cell-Free DNA Following Chemotherapy in Breast Cancer Patients</title><author>Adusei, Evelyn ; Ahenkorah, John ; Adu-Aryee, Nii Armah ; Adutwum-Ofosu, Kevin Kofi ; Tagoe, Emmanuel Ayitey ; Koney, Nii Koney-Kwaku ; Nkansah, Emmanuel ; Aryee, Nii Ayite ; Blay, Richard Michael ; Hottor, Bismarck Afedo ; Clegg-Lamptey, Joe-Nat ; Arko-Boham, Benjamin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3967-d990449ad90d507106ecab3fe0b154040c423497ce2b803f583417a77f70f09e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Apoptosis</topic><topic>biomarker</topic><topic>Biomarkers, Tumor - genetics</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Cancer therapies</topic><topic>Cell-Free Nucleic Acids</topic><topic>cfDNA</topic><topic>Chemotherapy</topic><topic>circulating cell-free DNA</topic><topic>DNA</topic><topic>Drugs</topic><topic>Female</topic><topic>Genomes</topic><topic>Health care</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Metastasis</topic><topic>Mortality</topic><topic>Neoadjuvant Therapy</topic><topic>RNA polymerase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Adusei, Evelyn</creatorcontrib><creatorcontrib>Ahenkorah, John</creatorcontrib><creatorcontrib>Adu-Aryee, Nii Armah</creatorcontrib><creatorcontrib>Adutwum-Ofosu, Kevin Kofi</creatorcontrib><creatorcontrib>Tagoe, Emmanuel Ayitey</creatorcontrib><creatorcontrib>Koney, Nii Koney-Kwaku</creatorcontrib><creatorcontrib>Nkansah, Emmanuel</creatorcontrib><creatorcontrib>Aryee, Nii Ayite</creatorcontrib><creatorcontrib>Blay, Richard Michael</creatorcontrib><creatorcontrib>Hottor, Bismarck Afedo</creatorcontrib><creatorcontrib>Clegg-Lamptey, Joe-Nat</creatorcontrib><creatorcontrib>Arko-Boham, Benjamin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>Medical sciences (Basel)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Adusei, Evelyn</au><au>Ahenkorah, John</au><au>Adu-Aryee, Nii Armah</au><au>Adutwum-Ofosu, Kevin Kofi</au><au>Tagoe, Emmanuel Ayitey</au><au>Koney, Nii Koney-Kwaku</au><au>Nkansah, Emmanuel</au><au>Aryee, Nii Ayite</au><au>Blay, Richard Michael</au><au>Hottor, Bismarck Afedo</au><au>Clegg-Lamptey, Joe-Nat</au><au>Arko-Boham, Benjamin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reduced Serum Circulation of Cell-Free DNA Following Chemotherapy in Breast Cancer Patients</atitle><jtitle>Medical sciences (Basel)</jtitle><addtitle>Med Sci (Basel)</addtitle><date>2021-05-25</date><risdate>2021</risdate><volume>9</volume><issue>2</issue><spage>37</spage><pages>37-</pages><issn>2076-3271</issn><eissn>2076-3271</eissn><abstract>Breast cancer is the most common malignancy in women, with alarming mortalities. Neoadjuvant treatments employ chemotherapy to shrink tumours to a well-defined size for a better surgical outcome. The current means of assessing effectiveness of chemotherapy management are imprecise. We previously showed that breast cancer patients have higher serum circulating cell-free DNA concentrations. cfDNA is degraded cellular DNA fragments released into the bloodstream. We further report on the utility of cfDNA in assessing the response to chemotherapy and its potential as a monitoring biomarker. A total of 32 newly diagnosed and treatment-naive female breast cancer patients and 32 healthy females as controls were included. Anthropometric, demographic and clinicopathological information of participants were recorded. Each participant donated 5 mL of venous blood from which sera were separated. Blood sampling was carried out before the commencement of chemotherapy (timepoint 1) and after the third cycle of chemotherapy (timepoint 2). qPCR was performed on the sera to quantify ALU 115 and 247 levels, and DNA integrity (ALU247/ALU115) was determined. ALU 115 and 247 levels were elevated in cancer patients but were significantly decreased after the third cycle of chemotherapy (T2) compared to T1. DNA integrity increased after the third cycle. 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subjects | Apoptosis biomarker Biomarkers, Tumor - genetics Breast cancer Breast Neoplasms - drug therapy Cancer therapies Cell-Free Nucleic Acids cfDNA Chemotherapy circulating cell-free DNA DNA Drugs Female Genomes Health care Hospitals Humans Metastasis Mortality Neoadjuvant Therapy RNA polymerase |
title | Reduced Serum Circulation of Cell-Free DNA Following Chemotherapy in Breast Cancer Patients |
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