Detection Methods and Clinical Applications of Circulating Tumor Cells in Breast Cancer
Circulating Tumor Cells (CTCs) are cancer cells that split away from the primary tumor and appear in the circulatory system as singular units or clusters, which was first reported by Dr. Thomas Ashworth in 1869. CTCs migrate and implantation occurs at a new site, in a process commonly known as tumor...
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Published in | Frontiers in oncology Vol. 11; p. 652253 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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02.06.2021
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Abstract | Circulating Tumor Cells (CTCs) are cancer cells that split away from the primary tumor and appear in the circulatory system as singular units or clusters, which was first reported by Dr. Thomas Ashworth in 1869. CTCs migrate and implantation occurs at a new site, in a process commonly known as tumor metastasis. In the case of breast cancer, the tumor cells often migrate into locations such as the lungs, brain, and bones, even during the early stages, and this is a notable characteristic of breast cancer. Survival rates have increased significantly over the past few decades because of progress made in radiology and tissue biopsy, making early detection and diagnosis of breast cancer possible. However, liquid biopsy, particularly that involving the collection of CTCs, is a non-invasive method to detect tumor cells in the circulatory system, which can be easily isolated from human plasma, serum, and other body fluids. Compared to traditional tissue biopsies, fluid sample collection has the advantages of being readily available and more acceptable to the patient. It can also detect tumor cells in blood earlier and in smaller numbers, possibly allowing for diagnosis prior to any tumor detection using imaging methods. Because of the scarcity of CTCs circulating in blood vessels (only a few CTCs among billions of erythrocytes and leukocytes), thorough but accurate detection methods are particularly important for further clinical applications. |
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AbstractList | Circulating Tumor Cells (CTCs) are cancer cells that split away from the primary tumor and appear in the circulatory system as singular units or clusters, which was first reported by Dr. Thomas Ashworth in 1869. CTCs migrate and implantation occurs at a new site, in a process commonly known as tumor metastasis. In the case of breast cancer, the tumor cells often migrate into locations such as the lungs, brain, and bones, even during the early stages, and this is a notable characteristic of breast cancer. Survival rates have increased significantly over the past few decades because of progress made in radiology and tissue biopsy, making early detection and diagnosis of breast cancer possible. However, liquid biopsy, particularly that involving the collection of CTCs, is a non-invasive method to detect tumor cells in the circulatory system, which can be easily isolated from human plasma, serum, and other body fluids. Compared to traditional tissue biopsies, fluid sample collection has the advantages of being readily available and more acceptable to the patient. It can also detect tumor cells in blood earlier and in smaller numbers, possibly allowing for diagnosis prior to any tumor detection using imaging methods. Because of the scarcity of CTCs circulating in blood vessels (only a few CTCs among billions of erythrocytes and leukocytes), thorough but accurate detection methods are particularly important for further clinical applications. Circulating Tumor Cells (CTCs) are cancer cells that split away from the primary tumor and appear in the circulatory system as singular units or clusters, which was first reported by Dr. Thomas Ashworth in 1869. CTCs migrate and implantation occurs at a new site, in a process commonly known as tumor metastasis. In the case of breast cancer, the tumor cells often migrate into locations such as the lungs, brain, and bones, even during the early stages, and this is a notable characteristic of breast cancer. Survival rates have increased significantly over the past few decades because of progress made in radiology and tissue biopsy, making early detection and diagnosis of breast cancer possible. However, liquid biopsy, particularly that involving the collection of CTCs, is a non-invasive method to detect tumor cells in the circulatory system, which can be easily isolated from human plasma, serum, and other body fluids. Compared to traditional tissue biopsies, fluid sample collection has the advantages of being readily available and more acceptable to the patient. It can also detect tumor cells in blood earlier and in smaller numbers, possibly allowing for diagnosis prior to any tumor detection using imaging methods. Because of the scarcity of CTCs circulating in blood vessels (only a few CTCs among billions of erythrocytes and leukocytes), thorough but accurate detection methods are particularly important for further clinical applications.Circulating Tumor Cells (CTCs) are cancer cells that split away from the primary tumor and appear in the circulatory system as singular units or clusters, which was first reported by Dr. Thomas Ashworth in 1869. CTCs migrate and implantation occurs at a new site, in a process commonly known as tumor metastasis. In the case of breast cancer, the tumor cells often migrate into locations such as the lungs, brain, and bones, even during the early stages, and this is a notable characteristic of breast cancer. Survival rates have increased significantly over the past few decades because of progress made in radiology and tissue biopsy, making early detection and diagnosis of breast cancer possible. However, liquid biopsy, particularly that involving the collection of CTCs, is a non-invasive method to detect tumor cells in the circulatory system, which can be easily isolated from human plasma, serum, and other body fluids. Compared to traditional tissue biopsies, fluid sample collection has the advantages of being readily available and more acceptable to the patient. It can also detect tumor cells in blood earlier and in smaller numbers, possibly allowing for diagnosis prior to any tumor detection using imaging methods. Because of the scarcity of CTCs circulating in blood vessels (only a few CTCs among billions of erythrocytes and leukocytes), thorough but accurate detection methods are particularly important for further clinical applications. |
Author | Smollar, Jillian Luis, Manuel A. Zhang, Hongyi Wan, Yuan Cai, Fengfeng Dique, Marcia R. Tang, Shasha Wang, Minghong Cai, Lu Lin, Xiaoyan Huang, Yuan Cen, Chunmei |
AuthorAffiliation | 3 Shanghai Public Health Clinical Center, Fudan University , Shanghai , China 4 Department of General Surgery, Zhongshan Hospital, Fudan University , Shanghai , China 2 Cellomics International Limited , Hong Kong , China 5 Department of Biomedical Engineering, The City College of New York , New York, NY , United States 1 Department of Breast Surgery, Yangpu Hospital, Tongji University School of Medicine , Shanghai , China |
AuthorAffiliation_xml | – name: 2 Cellomics International Limited , Hong Kong , China – name: 4 Department of General Surgery, Zhongshan Hospital, Fudan University , Shanghai , China – name: 3 Shanghai Public Health Clinical Center, Fudan University , Shanghai , China – name: 1 Department of Breast Surgery, Yangpu Hospital, Tongji University School of Medicine , Shanghai , China – name: 5 Department of Biomedical Engineering, The City College of New York , New York, NY , United States |
Author_xml | – sequence: 1 givenname: Hongyi surname: Zhang fullname: Zhang, Hongyi – sequence: 2 givenname: Xiaoyan surname: Lin fullname: Lin, Xiaoyan – sequence: 3 givenname: Yuan surname: Huang fullname: Huang, Yuan – sequence: 4 givenname: Minghong surname: Wang fullname: Wang, Minghong – sequence: 5 givenname: Chunmei surname: Cen fullname: Cen, Chunmei – sequence: 6 givenname: Shasha surname: Tang fullname: Tang, Shasha – sequence: 7 givenname: Marcia R. surname: Dique fullname: Dique, Marcia R. – sequence: 8 givenname: Lu surname: Cai fullname: Cai, Lu – sequence: 9 givenname: Manuel A. surname: Luis fullname: Luis, Manuel A. – sequence: 10 givenname: Jillian surname: Smollar fullname: Smollar, Jillian – sequence: 11 givenname: Yuan surname: Wan fullname: Wan, Yuan – sequence: 12 givenname: Fengfeng surname: Cai fullname: Cai, Fengfeng |
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Copyright | Copyright © 2021 Zhang, Lin, Huang, Wang, Cen, Tang, Dique, Cai, Luis, Smollar, Wan and Cai. Copyright © 2021 Zhang, Lin, Huang, Wang, Cen, Tang, Dique, Cai, Luis, Smollar, Wan and Cai 2021 Zhang, Lin, Huang, Wang, Cen, Tang, Dique, Cai, Luis, Smollar, Wan and Cai |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 Reviewed by: Ramray Bhat, Indian Institute of Science (IISc), India; Zuheir Alshehabi, Tishreen University, Syria Edited by: George Calin, University of Texas MD Anderson Cancer Center, United States This article was submitted to Molecular and Cellular Oncology, a section of the journal Frontiers in Oncology These authors have contributed equally to this work |
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