2022
DOI: 10.1016/j.gene.2022.146448
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Nanog, as a key cancer stem cell marker in tumor progression

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Cited by 46 publications
(21 citation statements)
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“…Gastric cancer stemness can be determined by investigating the expression of cell surface markers, namely CD24, CD44, and LGR5, and stemness-related transcriptional factors, namely Nanog and SOX2. Nanog is widely expressed in human cancer and is involved in self-renewal, metastasis, and chemoresistance [ 33 , 34 ]. SOX2 is involved in the maintenance of an undifferentiated cellular phenotype and often leads to increased chemotherapy resistance in cancer [ 35 , 36 ].…”
Section: Discussionmentioning
confidence: 99%
“…Gastric cancer stemness can be determined by investigating the expression of cell surface markers, namely CD24, CD44, and LGR5, and stemness-related transcriptional factors, namely Nanog and SOX2. Nanog is widely expressed in human cancer and is involved in self-renewal, metastasis, and chemoresistance [ 33 , 34 ]. SOX2 is involved in the maintenance of an undifferentiated cellular phenotype and often leads to increased chemotherapy resistance in cancer [ 35 , 36 ].…”
Section: Discussionmentioning
confidence: 99%
“…Cancer cells are not able to develop in certain body without the presence of stem cells. They first attack on stem cells and handle all their activities and by using single cell they start making tumor in the body [11]. The major cause of skin ovary cancer is still understudy because most of studies are going on this issue to calculate the exact reason of developing these tumors.…”
Section: Discussionmentioning
confidence: 99%
“…Some of these proteins, including OCT4, MYC, KLF4, and SOX2 (Yamanaka factors), are universal, considering that they are typical of both cancer and normal stem cells and are considered essential for stem-related phenotypes [ 107 ]. The regulation of other markers, though, for instance, NANOG, BMI-1, SNAIL, ALDHs, LGR5, CXCR4, REX-1, Musashi-1, LETM1, and C-met, is considered to be dependent on both the cancer type and the specific phenotype of the CSCs that we want to analyze (e.g., drug-resistant, tumorigenic, metastatic) [ 35 , 108 , 109 , 110 , 111 , 112 , 113 , 114 , 115 , 116 , 117 ]. Studying the expression of specific genes both at the transcriptional and translation level, as well as the activity and localization of these proteins, is useful in assessing the enrichment of CSC properties [ 118 , 119 , 120 , 121 , 122 , 123 ].…”
Section: Cancer Stem Cells (Cscs)mentioning
confidence: 99%