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Isolation and Functional Assessment of Human Breast Cancer Stem Cells from Cell and Tissue Samples
Published on: October 2, 2020
Nanotechniques Inactivate Cancer Stem Cells
Anatoliy N Goltsev1, Natalya N Babenko2, Yulia A Gaevskaya2
1Institute for Problems of Cryobiology and Cryomedicine of the National Academy of Sciences of Ukraine, Pereyaslavska Str. 23, Kharkiv, 61016, Ukraine. cryopato@gmail.com.
Abstract:
One of the tasks of current oncology is identification of cancer stem cells and search of therapeutic means capable of their specific inhibition. The paper presents the data on phenotype characteristics of Ehrlich carcinoma cells as convenient and easy-to-follow model of tumor growth. The evidence of cancer stem cells as a part of Ehrlich carcinoma and significance of CD44+ and CD44- subpopulations in maintaining the growth of this type of tumor were demonstrated. A high (tenfold) tumorigenic activity of the Ehrlich carcinoma CD44+ cells if compared to CD44- cells was proven. In this pair of comparison, the CD44+ cells had a higher potential of generating in peritoneal cavity of CD44high, CD44+CD24-, CD44+CD24+ cell subpopulations, highlighting the presence of cancer stem cells in a pool of CD44+ cells.In this study, the ability of synthesized hybrid nanocomplexes, comprising the nanoparticles of rare earth orthovanadates GdYVO4:Eu3+ and cholesterol to inhibit the tumor growth and to increase the survival of the animals with tumors was established. A special contribution into tumor-inhibiting effect is made by each of its components. Treatment of Ehrlich carcinoma cells with two-component hybrid complex resulted in maximum reduction in the concentration of the most tumorigenic CD44high cells with simultaneous rise in the number of CD117+ cells that decreased an intensity of tumor growth by 74.70 ± 4.38% if compared with the control.
Insights
This study identifies cancer stem cells within Ehrlich carcinoma, demonstrating CD44+ cells possess higher tumorigenic potential. Hybrid nanocomplexes effectively inhibited tumor growth by targeting these cancer stem cells.
Area of Science:
- Oncology
- Cancer Stem Cell Biology
- Nanomedicine
Background:
- Cancer stem cells (CSCs) are crucial for tumor growth and recurrence.
- Identifying CSCs and developing targeted therapies is a key challenge in oncology.
- Ehrlich carcinoma serves as a model to study CSCs and their therapeutic inhibition.
Purpose of the Study:
- To characterize Ehrlich carcinoma cells and identify CSCs.
- To evaluate the therapeutic potential of novel hybrid nanocomplexes for cancer treatment.
- To investigate the role of CD44+ and CD44- subpopulations in tumor growth.
Main Methods:
- Phenotypic characterization of Ehrlich carcinoma cells.
- Assessment of tumorigenic activity of CD44+ and CD44- subpopulations.
- Treatment with hybrid nanocomplexes (GdYVO4:Eu3+ and cholesterol).
- Flow cytometry analysis of cell subpopulations (CD44, CD24, CD117).
Main Results:
- Ehrlich carcinoma contains CSCs, with CD44+ cells exhibiting significantly higher tumorigenic activity (tenfold) than CD44- cells.
- CD44+ cells generated CD44high, CD44+CD24-, and CD44+CD24+ subpopulations, confirming CSC presence.
- Hybrid nanocomplex treatment reduced CD44high cells and increased CD117+ cells.
- Tumor growth intensity was reduced by 74.70% ± 4.38% in the treated group compared to the control.
Conclusions:
- Cancer stem cells are present in Ehrlich carcinoma and are enriched within the CD44+ subpopulation.
- Synthesized hybrid nanocomplexes demonstrate significant tumor-inhibiting effects.
- These nanocomplexes offer a promising therapeutic strategy by targeting cancer stem cells in Ehrlich carcinoma.
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