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Updated: Mar 20, 2026

Patient Derived Cell Culture and Isolation of CD133+ Putative Cancer Stem Cells from Melanoma
Published on: March 13, 2013
CD133, Selectively Targeting the Root of Cancer
Jörg U Schmohl1,2, Daniel A Vallera3
1University of Minnesota Masonic Cancer Center, Section of Molecular Cancer Therapeutics, Therapeutic Radiology-Radiation Oncology, University of Minnesota, Minneapolis, MN 55423, USA. jschmohl@gmx.de.
Targeting cancer stem cells (CSCs) via the CD133 marker shows promise. Novel biological agents using anti-CD133 single chain variable fragments (scFv) deliver toxins or immune components for CSC elimination.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Cancer stem cells (CSCs) drive tumor initiation, self-renewal, and chemotherapy resistance.
- Drug-refractory relapse is a major challenge in cancer research, often linked to CSCs.
- CD133 is a promising CSC marker, though not universally expressed.
Purpose of the Study:
- To review novel biological agents targeting CD133 for CSC elimination.
- To discuss two distinct approaches utilizing anti-CD133 single chain variable fragments (scFv).
Main Methods:
- Development of anti-CD133 scFv for targeted delivery.
- Utilizing scFv to deliver catalytic toxins to CSCs.
- Employing scFv to deliver immune system components for CSC targeting.
Main Results:
- Two distinct biological agent strategies targeting CD133 were investigated.
- Both approaches demonstrated high efficacy in selectively targeting CD133.
- The agents showed potential for specific and efficient CSC elimination.
Conclusions:
- Targeting CD133 with biological agents offers a promising strategy against CSCs.
- scFv-based delivery systems are effective for both toxin and immune component payloads.
- These CD133-associated agents present a novel therapeutic avenue for refractory cancers.
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