2021
DOI: 10.1002/ccr3.4498
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Merkel cell carcinoma on the right calf in association with chronic lymphocytic leukemia: A case report

Abstract: This is an open access article under the terms of the Creat ive Commo ns Attri bution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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Cited by 2 publications
(1 citation statement)
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“…The capacity of self‐renewal and differentiation into multiple cellular subtypes introduces CSCs as the source or origin of both tumor initiation and tumor maintenance in various cancers. TME‐associated stromal and non‐stromal cells more support tumorigenic function of CSCs through activation of survival‐supportive signaling pathways such as Wnt/β‐catenin, Hh, Notch, and NF‐κB and on the other hand CSCs‐derived immunomodulators (i.e., cytokines and chemokines), angiogenic factors (e.g., VEGF, vascular endothelial growth factor), and metastatic factors (e.g., MMP‐2, matrix metalloproteinase‐2) lead to recruitment of tumor‐supportive immune cells, activation of angiogenesis, and promotion of tumor metastasis 10,11 . Various mechanisms of radio/chemoresistance in CSCs have emerged, resulting in the development of specific approaches for CSC‐directed immunotherapies including: (i) monoclonal and bispecific antibodies targeting CSCs surface biomarkers (e.g., CD44v6, CD44, CD123, EGFR, EpCAM, and CD133) or immune checkpoint molecules using immune checkpoint inhibitors (ICIs) (e.g., Letaplimab against CD47), (ii) adoptive cell therapy in the format of chimeric antigen receptor (CAR) T‐cells and CAR NK‐cells, and (iii) CSCs‐based vaccines 12 (Figure 1 and Table 1).…”
Section: Stemness Factors and Immunotherapy Resistancementioning
confidence: 99%
“…The capacity of self‐renewal and differentiation into multiple cellular subtypes introduces CSCs as the source or origin of both tumor initiation and tumor maintenance in various cancers. TME‐associated stromal and non‐stromal cells more support tumorigenic function of CSCs through activation of survival‐supportive signaling pathways such as Wnt/β‐catenin, Hh, Notch, and NF‐κB and on the other hand CSCs‐derived immunomodulators (i.e., cytokines and chemokines), angiogenic factors (e.g., VEGF, vascular endothelial growth factor), and metastatic factors (e.g., MMP‐2, matrix metalloproteinase‐2) lead to recruitment of tumor‐supportive immune cells, activation of angiogenesis, and promotion of tumor metastasis 10,11 . Various mechanisms of radio/chemoresistance in CSCs have emerged, resulting in the development of specific approaches for CSC‐directed immunotherapies including: (i) monoclonal and bispecific antibodies targeting CSCs surface biomarkers (e.g., CD44v6, CD44, CD123, EGFR, EpCAM, and CD133) or immune checkpoint molecules using immune checkpoint inhibitors (ICIs) (e.g., Letaplimab against CD47), (ii) adoptive cell therapy in the format of chimeric antigen receptor (CAR) T‐cells and CAR NK‐cells, and (iii) CSCs‐based vaccines 12 (Figure 1 and Table 1).…”
Section: Stemness Factors and Immunotherapy Resistancementioning
confidence: 99%