Cancer stem cells as key drivers of tumour progression
Open accessAbstract
BACKGROUND: Cancer stem cells (CSCs) are subpopulations of cancer cells sharing similar characteristics as normal stem or progenitor cells such as self-renewal ability and multi-lineage differentiation to drive tumour growth and heterogeneity. Throughout the cancer progression, CSC can further be induced from differentiated cancer cells via the adaptation and cross-talks with the tumour microenvironment as well as a response from therapeutic pressures, therefore contributes to their heterogeneous phenotypes. Challengingly, conventional cancer treatments target the bulk of the tumour and are unable to target CSCs due to their highly resistance nature, leading to metastasis and tumour recurrence. MAIN BODY: This review highlights the roles of CSCs in tumour initiation, progression and metastasis with a focus on the cellular and molecular regulators that influence their phenotypical changes and behaviours in the different stages of cancer progression. We delineate the cross-talks between CSCs with the tumour microenvironment that support their intrinsic properties including survival, stemness, quiescence and their cellular and molecular adaptation in response to therapeutic pressure. An insight into the distinct roles of CSCs in promoting angiogenesis and metastasis has been captured based on in vitro and in vivo evidences. CONCLUSION: Given dynamic cellular events along the cancer progression and contributions of resistance nature by CSCs, understanding their molecular and cellular regulatory mechanism in a heterogeneous nature, provides significant cornerstone for the development of CSC-specific therapeutics.
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Molecular markers of CSCs are used for diagnosis and have therapeutic value because they are implicated in oncogenesis.
“Molecular markers of CSCs are not only used for diagnosis, but also have a therapeutic value because they are implicated in oncogenesis [84].”
From 20-Hydroxyecdysone Confers Antioxidant and Antineoplastic Properties in Human Non-Small Cell Lung Cancer Cells (2023) · cites this paper as [84]
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References 210 · Cited by 910
- Authors
- Ayob, A. Z., & Ramasamy, T. S.
- Affiliations
- University of Malaya (MY)
- Corresponding author
- Ramasamy, Thamil Selvee
- Venue
- Journal of Biomedical Science
- Published
- 2018-03-06
- Volume
- 25
- Issue
- 1
- Pages
- 20-20
- ISSN
- 1021-7770 (ISSN-L)
- 1423-0127
- PMC
- PMC5838954
- OpenAlex
- W2801437236
- Cited by
- 910
- References
- 210
- Citations by year
- 2026: 39 · 2025: 100 · 2024: 126 · 2023: 161 · 2022: 152 · 2021: 166 · 2020: 101 · 2019: 47 · 2018: 17
- FWCI
- 8.67
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Licence
- cc-by
- Locations
- Journal of Biomedical Science (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Universiti Malaya (RP032-14HTM)
- Topics
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Health Sciences › Medicine › Genetics › Mesenchymal stem cell research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- cancer stem cells, tumor progression, tumor heterogeneity, tumor microenvironment, stemness, quiescence, treatment resistance, metastasis, angiogenesis, tumor recurrence, self-renewal, multilineage differentiation
- MeSH terms
- Cell Differentiation, Neoplasms, Neoplastic Stem Cells, Gene Expression Regulation, Neoplastic, Tumor Microenvironment
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