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An Image-Based Identification of Aggressive Breast Cancer Circulating Tumor Cell Subtypes

SIMPLE SUMMARY: The majority of cancer-related deaths are attributed to distant metastases—the spread of cancer to different parts of the body. Accurate and early prediction of metastasis and response to therapy is key for the better management of cancer. Although metastases were initiated by circul...

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Autores principales: Kamal, Mohamed, Wang, Yiru Jess, Plummer, Sarai, Dickerson, Amber, Yu, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216536/
https://www.ncbi.nlm.nih.gov/pubmed/37345005
http://dx.doi.org/10.3390/cancers15102669
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author Kamal, Mohamed
Wang, Yiru Jess
Plummer, Sarai
Dickerson, Amber
Yu, Min
author_facet Kamal, Mohamed
Wang, Yiru Jess
Plummer, Sarai
Dickerson, Amber
Yu, Min
author_sort Kamal, Mohamed
collection PubMed
description SIMPLE SUMMARY: The majority of cancer-related deaths are attributed to distant metastases—the spread of cancer to different parts of the body. Accurate and early prediction of metastasis and response to therapy is key for the better management of cancer. Although metastases were initiated by circulating tumor cells (CTCs) shed into the bloodstream, only a small subset of CTCs bears metastatic capacity. Since cellular morphology has been shown to reflect cell state and function, we aim to detect the metastasis-initiating subpopulation of CTCs through a simple image analysis. We performed deep morphometric analyses of CTCs and determined their metastatic potential in mice. We identified a subgroup of CTCs with small size, large mitochondria and rough membrane texture to have the highest tumorigenic potential. Our new findings provide a simple image-based identification of CTC subpopulations with elevated aggressiveness, which is expected to provide a more accurate prediction of breast cancer patient survival than total CTC numbers. ABSTRACT: Using previously established CTC lines from breast cancer patients, we identified different morphometric subgroups of CTCs with one of them having the highest tumorigenic potential in vivo despite the slowest cell proliferation in vitro. This subgroup represents 32% of all cells and contains cells with small cell volume, large nucleus to cell, dense nuclear areas to the nucleus, mitochondria to cell volume ratios and rough texture of cell membrane and termed “Small cell, Large mitochondria, Rough membrane” (SLR). RNA-seq analyses showed that the SLR group is enriched in pathways and cellular processes related to DNA replication, DNA repair and metabolism. SLR upregulated genes are associated with poor survival in patients with ER+ breast cancer based on the KM Plotter database. The high tumorigenic potential, slow proliferation, and enriched DNA replication/repair pathways suggest that the SLR subtype is associated with stemness properties. Our new findings provide a simple image-based identification of CTC subpopulations with elevated aggressiveness, which is expected to provide a more accurate prediction of patient survival and therapy response than total CTC numbers. The detection of morphometric and transcriptomic profiles related to the SLR subgroup of CTCs also opens opportunities for potential targeted cancer treatment.
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spelling pubmed-102165362023-05-27 An Image-Based Identification of Aggressive Breast Cancer Circulating Tumor Cell Subtypes Kamal, Mohamed Wang, Yiru Jess Plummer, Sarai Dickerson, Amber Yu, Min Cancers (Basel) Article SIMPLE SUMMARY: The majority of cancer-related deaths are attributed to distant metastases—the spread of cancer to different parts of the body. Accurate and early prediction of metastasis and response to therapy is key for the better management of cancer. Although metastases were initiated by circulating tumor cells (CTCs) shed into the bloodstream, only a small subset of CTCs bears metastatic capacity. Since cellular morphology has been shown to reflect cell state and function, we aim to detect the metastasis-initiating subpopulation of CTCs through a simple image analysis. We performed deep morphometric analyses of CTCs and determined their metastatic potential in mice. We identified a subgroup of CTCs with small size, large mitochondria and rough membrane texture to have the highest tumorigenic potential. Our new findings provide a simple image-based identification of CTC subpopulations with elevated aggressiveness, which is expected to provide a more accurate prediction of breast cancer patient survival than total CTC numbers. ABSTRACT: Using previously established CTC lines from breast cancer patients, we identified different morphometric subgroups of CTCs with one of them having the highest tumorigenic potential in vivo despite the slowest cell proliferation in vitro. This subgroup represents 32% of all cells and contains cells with small cell volume, large nucleus to cell, dense nuclear areas to the nucleus, mitochondria to cell volume ratios and rough texture of cell membrane and termed “Small cell, Large mitochondria, Rough membrane” (SLR). RNA-seq analyses showed that the SLR group is enriched in pathways and cellular processes related to DNA replication, DNA repair and metabolism. SLR upregulated genes are associated with poor survival in patients with ER+ breast cancer based on the KM Plotter database. The high tumorigenic potential, slow proliferation, and enriched DNA replication/repair pathways suggest that the SLR subtype is associated with stemness properties. Our new findings provide a simple image-based identification of CTC subpopulations with elevated aggressiveness, which is expected to provide a more accurate prediction of patient survival and therapy response than total CTC numbers. The detection of morphometric and transcriptomic profiles related to the SLR subgroup of CTCs also opens opportunities for potential targeted cancer treatment. MDPI 2023-05-09 /pmc/articles/PMC10216536/ /pubmed/37345005 http://dx.doi.org/10.3390/cancers15102669 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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/).
spellingShingle Article
Kamal, Mohamed
Wang, Yiru Jess
Plummer, Sarai
Dickerson, Amber
Yu, Min
An Image-Based Identification of Aggressive Breast Cancer Circulating Tumor Cell Subtypes
title An Image-Based Identification of Aggressive Breast Cancer Circulating Tumor Cell Subtypes
title_full An Image-Based Identification of Aggressive Breast Cancer Circulating Tumor Cell Subtypes
title_fullStr An Image-Based Identification of Aggressive Breast Cancer Circulating Tumor Cell Subtypes
title_full_unstemmed An Image-Based Identification of Aggressive Breast Cancer Circulating Tumor Cell Subtypes
title_short An Image-Based Identification of Aggressive Breast Cancer Circulating Tumor Cell Subtypes
title_sort image-based identification of aggressive breast cancer circulating tumor cell subtypes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216536/
https://www.ncbi.nlm.nih.gov/pubmed/37345005
http://dx.doi.org/10.3390/cancers15102669
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