Dynamics of Phenotypic Heterogeneity Associated with EMT and Stemness during Cancer Progression
Jolly, Mohit Kumar (Indian Institute of Science)
Celià-Terrassa, Toni 
(Institut Hospital del Mar d'Investigacions Mèdiques)
| Data: |
2019 |
| Resum: |
Genetic and phenotypic heterogeneity contribute to the generation of diverse tumor cell populations, thus enhancing cancer aggressiveness and therapy resistance. Compared to genetic heterogeneity, a consequence of mutational events, phenotypic heterogeneity arises from dynamic, reversible cell state transitions in response to varying intracellular/extracellular signals. Such phenotypic plasticity enables rapid adaptive responses to various stressful conditions and can have a strong impact on cancer progression. Herein, we have reviewed relevant literature on mechanisms associated with dynamic phenotypic changes and cellular plasticity, such as epithelial-mesenchymal transition (EMT) and cancer stemness, which have been reported to facilitate cancer metastasis. We also discuss how non-cell-autonomous mechanisms such as cell-cell communication can lead to an emergent population-level response in tumors. The molecular mechanisms underlying the complexity of tumor systems are crucial for comprehending cancer progression, and may provide new avenues for designing therapeutic strategies. |
| Ajuts: |
Instituto de Salud Carlos III MS17/00037 Instituto de Salud Carlos III PI18/00014
|
| Drets: |
Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.  |
| Llengua: |
Anglès |
| Document: |
Article ; recerca ; Versió publicada |
| Matèria: |
Cellular dynamics ;
Epithelial-to-mesenchymal transition ;
Cell plasticity ;
Cancer stem cells ;
Mathematical modeling ;
Population homeostasis |
| Publicat a: |
Journal of clinical medicine, Vol. 8 (september 2019) , ISSN 2077-0383 |
DOI: 10.3390/jcm8101542
PMID: 31557977
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