scholarly journals Colorectal cancer stem cells: a review of targeted drug delivery by gold nanoparticles

RSC Advances ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 973-985 ◽  
Author(s):  
Manali Haniti Mohd-Zahid ◽  
Rohimah Mohamud ◽  
Che Azurahanim Che Abdullah ◽  
JitKang Lim ◽  
Halima Alem ◽  
...  
Keyword(s):  
Colorectal Cancer ◽  
Drug Delivery ◽  
Stem Cells ◽  
Gold Nanoparticles ◽  
Cancer Stem Cells ◽  
Targeted Drug Delivery ◽  
Targeted Drug ◽  
Colorectal Cancer Stem Cells

The proposed schematic mechanism via which 5-fluorouracil-loaded gold nanoparticles conjugated with CD133 antibody target colorectal cancer stem cells.

Nanomaterials for targeted drug delivery to cancer stem cells

2014 ◽  
Vol 46 (2) ◽  
pp. 191-206 ◽  
Author(s):  
Anamaria Orza ◽  
Daniel Casciano ◽  
Alexandru Biris
Keyword(s):  
Drug Delivery ◽  
Stem Cells ◽  
Cancer Stem Cells ◽  
Targeted Drug Delivery ◽  
Targeted Drug

scholarly journals Magnetic Nanoparticle-Based Hyperthermia Mediates Drug Delivery and Impairs the Tumorigenic Capacity of Quiescent Colorectal Cancer Stem Cells

2021 ◽  
Vol 13 (14) ◽  
pp. 15959-15972
Author(s):  
Soraia Fernandes ◽  
Tamara Fernandez ◽  
Sabrina Metze ◽  
Preethi B. Balakrishnan ◽  
Binh T. Mai ◽  
...  
Keyword(s):  
Colorectal Cancer ◽  
Drug Delivery ◽  
Stem Cells ◽  
Cancer Stem Cells ◽  
Magnetic Nanoparticle ◽  
Colorectal Cancer Stem Cells

Cancer stem cells and strategies for targeted drug delivery

2020 ◽  
Author(s):  
Jin Cao ◽  
Shubhmita Bhatnagar ◽  
Jiawei Wang ◽  
Xueyong Qi ◽  
Swayam Prabha ◽  
...  
Keyword(s):  
Drug Delivery ◽  
Stem Cells ◽  
Cancer Stem Cells ◽  
Targeted Drug Delivery ◽  
Targeted Drug

scholarly journals The microRNA-210-Stathmin1 Axis Decreases Cell Stiffness to Facilitate the Invasiveness of Colorectal Cancer Stem Cells

Cancers ◽  
2021 ◽  
Vol 13 (8) ◽  
pp. 1833
Author(s):  
Tsai-Tsen Liao ◽  
Wei-Chung Cheng ◽  
Chih-Yung Yang ◽  
Yin-Quan Chen ◽  
Shu-Han Su ◽  
...  
Keyword(s):  
Colorectal Cancer ◽  
Stem Cells ◽  
Cancer Stem Cells ◽  
Cell Motility ◽  
Cancer Cells ◽  
Epithelial Mesenchymal Transition ◽  
Cell Stiffness ◽  
Mesenchymal Transition ◽  
Cytoskeletal Dynamics ◽  
Colorectal Cancer Stem Cells

Cell migration is critical for regional dissemination and distal metastasis of cancer cells, which remain the major causes of poor prognosis and death in patients with colorectal cancer (CRC). Although cytoskeletal dynamics and cellular deformability contribute to the migration of cancer cells and metastasis, the mechanisms governing the migratory ability of cancer stem cells (CSCs), a nongenetic source of tumor heterogeneity, are unclear. Here, we expanded colorectal CSCs (CRCSCs) as colonospheres and showed that CRCSCs exhibited higher cell motility in transwell migration assays and 3D invasion assays and greater deformability in particle tracking microrheology than did their parental CRC cells. Mechanistically, in CRCSCs, microRNA-210-3p (miR-210) targeted stathmin1 (STMN1), which is known for inducing microtubule destabilization, to decrease cell elasticity in order to facilitate cell motility without affecting the epithelial–mesenchymal transition (EMT) status. Clinically, the miR-210-STMN1 axis was activated in CRC patients with liver metastasis and correlated with a worse clinical outcome. This study elucidates a miRNA-oriented mechanism regulating the deformability of CRCSCs beyond the EMT process.

PEG-poly(amino acid)s/EpCAM aptamer multifunctional nanoparticles arrest the growth and metastasis of colorectal cancer

2021 ◽  
Author(s):  
Yingru Zhang ◽  
Chunpu Li ◽  
Ru Jia ◽  
Ruixuan Gao ◽  
Yiyang Zhao ◽  
...  
Keyword(s):  
Colorectal Cancer ◽  
Stem Cells ◽  
Amino Acid ◽  
Cancer Stem Cells ◽  
Drug Release ◽  
Signaling Pathway ◽  
Water Solubility ◽  
Sustained Drug Release ◽  
Colorectal Cancer Stem Cells ◽  
Micelle System

A new nano-micelle system with better water solubility and sustained drug release effect, targeting colorectal cancer stem cells, effectively inhibits the growth and metastasis of colorectal cancer via the Wnt/β-catenin signaling pathway.

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