Characterization of stem-like cancer cells in basal cell carcinoma and its surgical margins
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Milošević, Maja
Lazarević, Miloš

Toljić, Boško

Simonović, Jelena
Trišić, Dijana

Nikolić, Nadja

Petrović, Milan

Milašin, Jelena

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BackgroundUnderstanding the pathogenesis of basal cell carcinoma (BCC) and identifying the cells responsible for propagation and recurrence are crucial for the development of new treatment strategies. The aim of this study was to characterize the cells isolated from BCC and its margin. MethodsPrimary cultures were established from 10 BCCs, their respective close resection margins (3mm) and 10 control tissues. Stem cell markers analysis was carried out by real-time PCR and/or flow cytometry. Spheroid formation and MTT assays were also performed. ResultsReal-time PCR showed a higher expression of embryonic (Oct4, Sox2 and Nanog) and mesenchymal (CD44 and CD73) stem cell markers in tumors compared to margins and controls (P lt 0.05). Bmi-1 and GPR49 were also upregulated in tumors in comparison with margins. Both tumor and margin cells, but not normal, had the capacity to form spheroids. During passages, the number of spheres increased, while the diameter decreased. Tumor cells showed hig...her chemo-resistance compared to margin and control cells. ConclusionsBasal cell carcinomas expressed stem cell markers, pointing to the existence of a cancer cell side population with stemness characteristics. Margin also appeared to harbour a small number of cancer-initiating cells.
Keywords:
basal cell carcinoma / embryonic and mesenchymal markers / neoplastic stem cells / surgical marginSource:
Experimental Dermatology, 2018, 27, 10, 1160-1165Publisher:
- Wiley, Hoboken
Funding / projects:
DOI: 10.1111/exd.13755
ISSN: 0906-6705
PubMed: 30033544
WoS: 000445727200013
Scopus: 2-s2.0-85052578159
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Stomatološki fakultetTY - JOUR AU - Milošević, Maja AU - Lazarević, Miloš AU - Toljić, Boško AU - Simonović, Jelena AU - Trišić, Dijana AU - Nikolić, Nadja AU - Petrović, Milan AU - Milašin, Jelena PY - 2018 UR - https://smile.stomf.bg.ac.rs/handle/123456789/2279 AB - BackgroundUnderstanding the pathogenesis of basal cell carcinoma (BCC) and identifying the cells responsible for propagation and recurrence are crucial for the development of new treatment strategies. The aim of this study was to characterize the cells isolated from BCC and its margin. MethodsPrimary cultures were established from 10 BCCs, their respective close resection margins (3mm) and 10 control tissues. Stem cell markers analysis was carried out by real-time PCR and/or flow cytometry. Spheroid formation and MTT assays were also performed. ResultsReal-time PCR showed a higher expression of embryonic (Oct4, Sox2 and Nanog) and mesenchymal (CD44 and CD73) stem cell markers in tumors compared to margins and controls (P lt 0.05). Bmi-1 and GPR49 were also upregulated in tumors in comparison with margins. Both tumor and margin cells, but not normal, had the capacity to form spheroids. During passages, the number of spheres increased, while the diameter decreased. Tumor cells showed higher chemo-resistance compared to margin and control cells. ConclusionsBasal cell carcinomas expressed stem cell markers, pointing to the existence of a cancer cell side population with stemness characteristics. Margin also appeared to harbour a small number of cancer-initiating cells. PB - Wiley, Hoboken T2 - Experimental Dermatology T1 - Characterization of stem-like cancer cells in basal cell carcinoma and its surgical margins VL - 27 IS - 10 SP - 1160 EP - 1165 DO - 10.1111/exd.13755 ER -
@article{ author = "Milošević, Maja and Lazarević, Miloš and Toljić, Boško and Simonović, Jelena and Trišić, Dijana and Nikolić, Nadja and Petrović, Milan and Milašin, Jelena", year = "2018", abstract = "BackgroundUnderstanding the pathogenesis of basal cell carcinoma (BCC) and identifying the cells responsible for propagation and recurrence are crucial for the development of new treatment strategies. The aim of this study was to characterize the cells isolated from BCC and its margin. MethodsPrimary cultures were established from 10 BCCs, their respective close resection margins (3mm) and 10 control tissues. Stem cell markers analysis was carried out by real-time PCR and/or flow cytometry. Spheroid formation and MTT assays were also performed. ResultsReal-time PCR showed a higher expression of embryonic (Oct4, Sox2 and Nanog) and mesenchymal (CD44 and CD73) stem cell markers in tumors compared to margins and controls (P lt 0.05). Bmi-1 and GPR49 were also upregulated in tumors in comparison with margins. Both tumor and margin cells, but not normal, had the capacity to form spheroids. During passages, the number of spheres increased, while the diameter decreased. Tumor cells showed higher chemo-resistance compared to margin and control cells. ConclusionsBasal cell carcinomas expressed stem cell markers, pointing to the existence of a cancer cell side population with stemness characteristics. Margin also appeared to harbour a small number of cancer-initiating cells.", publisher = "Wiley, Hoboken", journal = "Experimental Dermatology", title = "Characterization of stem-like cancer cells in basal cell carcinoma and its surgical margins", volume = "27", number = "10", pages = "1160-1165", doi = "10.1111/exd.13755" }
Milošević, M., Lazarević, M., Toljić, B., Simonović, J., Trišić, D., Nikolić, N., Petrović, M.,& Milašin, J.. (2018). Characterization of stem-like cancer cells in basal cell carcinoma and its surgical margins. in Experimental Dermatology Wiley, Hoboken., 27(10), 1160-1165. https://doi.org/10.1111/exd.13755
Milošević M, Lazarević M, Toljić B, Simonović J, Trišić D, Nikolić N, Petrović M, Milašin J. Characterization of stem-like cancer cells in basal cell carcinoma and its surgical margins. in Experimental Dermatology. 2018;27(10):1160-1165. doi:10.1111/exd.13755 .
Milošević, Maja, Lazarević, Miloš, Toljić, Boško, Simonović, Jelena, Trišić, Dijana, Nikolić, Nadja, Petrović, Milan, Milašin, Jelena, "Characterization of stem-like cancer cells in basal cell carcinoma and its surgical margins" in Experimental Dermatology, 27, no. 10 (2018):1160-1165, https://doi.org/10.1111/exd.13755 . .