RGD Density on Tadpole Nanostructures Regulates Cancer Stem Cell Proliferation and Stemness.
Dayong ZhangBing SunJingyi WangSung-Po R ChenValentin A BobrinYushu GuChun Ki NgWen-Yi GuMichael J MonteiroPublished in: Biomacromolecules (2024)
Cancer stem cells (CSCs) make up a small population of cancer cells, primarily responsible for tumor initiation, metastasis, and drug resistance. They overexpress Arg-Gly-Asp (RGD) binding integrin receptors that play crucial roles in cell proliferation and stemness through interaction with the extracellular matrix. Here, we showed that monodisperse polymeric tadpole nanoparticles covalently coupled with different RGD densities regulated colon CSC proliferation and stemness in a RGD density-dependent manner. These tadpoles penetrated deeply and evenly into tumor spheroids and specifically entered cells with cancer stem markers CD24 and CD133. Low RGD density tadpoles triggered integrin α5 expression that further activated TGF-β3 and TGF-β2 signaling pathways, confirmed by the increase of pERK and Bcl-2 protein levels. This process is associated with the RGD cluster presentation controlled by the RGD density on the tadpole surface.
Keyphrases
- cancer stem cells
- cell proliferation
- extracellular matrix
- stem cells
- epithelial mesenchymal transition
- signaling pathway
- papillary thyroid
- induced apoptosis
- transforming growth factor
- poor prognosis
- pi k akt
- squamous cell
- drug delivery
- cell cycle
- squamous cell carcinoma
- cancer therapy
- long non coding rna
- cell cycle arrest
- endoplasmic reticulum
- cell migration
- childhood cancer
- cell adhesion