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Published on: March 13, 2013
Decoding the Role of CD271 in Melanoma
1Department of Biomedical Sciences, University of Veterinary Medicine, Institute of Medical Biochemistry (HA/I), Veterinärplatz 1, 1210 Vienna, Austria.
Abstract:
The evolution of melanoma, the most aggressive type of skin cancer, is triggered by driver mutations that are acquired in the coding regions of particularly BRAF (rat fibrosarcoma serine/threonine kinase, isoform B) or NRAS (neuroblastoma-type ras sarcoma virus) in melanocytes. Although driver mutations strongly determine tumor progression, additional factors are likely required and prerequisite for melanoma formation. Melanocytes are formed during vertebrate development in a well-controlled differentiation process of multipotent neural crest stem cells (NCSCs). However, mechanisms determining the properties of melanocytes and melanoma cells are still not well understood. The nerve growth factor receptor CD271 is likewise expressed in melanocytes, melanoma cells and NCSCs and programs the maintenance of a stem-like and migratory phenotype via a comprehensive network of associated genes. Moreover, CD271 regulates phenotype switching, a process that enables the rapid and reversible conversion of proliferative into invasive or non-stem-like states into stem-like states by yet largely unknown mechanisms. Here, we summarize current findings about CD271-associated mechanisms in melanoma cells and illustrate the role of CD271 for melanoma cell migration and metastasis, phenotype-switching, resistance to therapeutic interventions, and the maintenance of an NCSC-like state.
Insights
The nerve growth factor receptor CD271 maintains stem-like traits in melanoma cells, influencing migration, metastasis, and therapeutic resistance. Understanding CD271 is crucial for targeting aggressive skin cancer progression.
Area of Science:
- Oncology
- Cell Biology
- Dermatology
Background:
- Melanoma, an aggressive skin cancer, arises from melanocytes, which develop from neural crest stem cells (NCSCs).
- While BRAF or NRAS mutations drive melanoma, other factors are essential for its formation and progression.
- The nerve growth factor receptor CD271 is expressed in melanocytes, melanoma cells, and NCSCs, regulating stem-like and migratory properties.
Purpose of the Study:
- To summarize current findings on CD271-associated mechanisms in melanoma cells.
- To illustrate the role of CD271 in melanoma cell migration, metastasis, and phenotype switching.
- To highlight CD271's involvement in therapeutic resistance and maintaining NCSC-like states in melanoma.
Main Methods:
- Literature review and synthesis of current research findings.
- Analysis of CD271's role in gene networks associated with stem-like phenotypes.
- Examination of CD271's impact on melanoma cell behavior, including migration and phenotype switching.
Main Results:
- CD271 programs a stem-like and migratory phenotype in melanoma cells through a network of associated genes.
- CD271 regulates phenotype switching, enabling transitions between proliferative and invasive states.
- CD271 contributes to melanoma cell migration, metastasis, therapeutic resistance, and maintenance of NCSC-like characteristics.
Conclusions:
- CD271 plays a critical role in melanoma progression by maintaining stem-like properties and driving key cellular processes.
- Targeting CD271 may offer therapeutic strategies for overcoming melanoma metastasis and treatment resistance.
- Further research into CD271-associated mechanisms is vital for understanding and combating aggressive melanoma.
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