Breast Cancer Stem Cell Membrane Biomarkers: Therapy Targeting and Clinical Implications.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
09 03 2022
Historique:
received: 12 01 2022
revised: 28 02 2022
accepted: 03 03 2022
entrez: 25 3 2022
pubmed: 26 3 2022
medline: 14 4 2022
Statut: epublish

Résumé

Breast cancer is the most common malignancy affecting women worldwide. Importantly, there have been significant improvements in prevention, early diagnosis, and treatment options, which resulted in a significant decrease in breast cancer mortality rates. Nevertheless, the high rates of incidence combined with therapy resistance result in cancer relapse and metastasis, which still contributes to unacceptably high mortality of breast cancer patients. In this context, a small subpopulation of highly tumourigenic cancer cells within the tumour bulk, commonly designated as breast cancer stem cells (BCSCs), have been suggested as key elements in therapy resistance, which are responsible for breast cancer relapses and distant metastasis. Thus, improvements in BCSC-targeting therapies are crucial to tackling the metastatic progression and might allow therapy resistance to be overcome. However, the design of effective and specific BCSC-targeting therapies has been challenging since there is a lack of specific biomarkers for BCSCs, and the most common clinical approaches are designed for commonly altered BCSCs signalling pathways. Therefore, the search for a new class of BCSC biomarkers, such as the expression of membrane proteins with cancer stem cell potential, is an area of clinical relevance, once membrane proteins are accessible on the cell surface and easily recognized by specific antibodies. Here, we discuss the significance of BCSC membrane biomarkers as potential prognostic and therapeutic targets, reviewing the CSC-targeting therapies under clinical trials for breast cancer.

Identifiants

pubmed: 35326385
pii: cells11060934
doi: 10.3390/cells11060934
pmc: PMC8946706
pii:
doi:

Substances chimiques

Biomarkers 0
Membrane Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Fundação para a Ciência e Tecnologia
ID : FCT/02/SAICT/2017/030625

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Auteurs

Inês Conde (I)

i3S, Institute of Investigation and Innovation in Health, 4200-135 Porto, Portugal.
Ipatimup, Institute of Molecular Pathology and Immunology, University of Porto, 4200-135 Porto, Portugal.

Ana Sofia Ribeiro (AS)

i3S, Institute of Investigation and Innovation in Health, 4200-135 Porto, Portugal.
Ipatimup, Institute of Molecular Pathology and Immunology, University of Porto, 4200-135 Porto, Portugal.

Joana Paredes (J)

i3S, Institute of Investigation and Innovation in Health, 4200-135 Porto, Portugal.
Ipatimup, Institute of Molecular Pathology and Immunology, University of Porto, 4200-135 Porto, Portugal.
Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal.

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