2011
DOI: 10.1053/j.gastro.2011.04.008
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SNAIL Regulates Interleukin-8 Expression, Stem Cell–Like Activity, and Tumorigenicity of Human Colorectal Carcinoma Cells

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Cited by 269 publications
(229 citation statements)
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“…In fact, simply overexpressing certain oncogenic molecules (e.g., Nanog, CD44, Twist, hTERT, etc) is sufficient to reprogram primary non-tumorigenic cells or bulk cancer cells into stem-like cancer cells [136][137][138][139][140][141]. These latter observations [136][137][138][139][140][141] are consistent with the observations that such 'stemness' molecules are most frequently expressed in undifferentiated tumor cells. Finally, as CSCs constantly interact with their microenvironment, protumorigenic alterations in the microenvironment (e.g., in stromal cells) will likely affect CSC properties and promote plasticity in CSC progeny [142,143].…”
Section: Intrinsic and Induced Plasticity In Csc Progenysupporting
confidence: 79%
See 1 more Smart Citation
“…In fact, simply overexpressing certain oncogenic molecules (e.g., Nanog, CD44, Twist, hTERT, etc) is sufficient to reprogram primary non-tumorigenic cells or bulk cancer cells into stem-like cancer cells [136][137][138][139][140][141]. These latter observations [136][137][138][139][140][141] are consistent with the observations that such 'stemness' molecules are most frequently expressed in undifferentiated tumor cells. Finally, as CSCs constantly interact with their microenvironment, protumorigenic alterations in the microenvironment (e.g., in stromal cells) will likely affect CSC properties and promote plasticity in CSC progeny [142,143].…”
Section: Intrinsic and Induced Plasticity In Csc Progenysupporting
confidence: 79%
“…Experimental EMT and inflammatory cytokines IL-6, IL-8, TGFβ, and TNFα can all promote the manifestation of CSC phenotypes and properties [130][131][132][133][134][135]. In fact, simply overexpressing certain oncogenic molecules (e.g., Nanog, CD44, Twist, hTERT, etc) is sufficient to reprogram primary non-tumorigenic cells or bulk cancer cells into stem-like cancer cells [136][137][138][139][140][141]. These latter observations [136][137][138][139][140][141] are consistent with the observations that such 'stemness' molecules are most frequently expressed in undifferentiated tumor cells.…”
Section: Intrinsic and Induced Plasticity In Csc Progenymentioning
confidence: 99%
“…IL-8 is often found upregulated in certain types of cancers and has been suspected to promote CSC's growth. Inhibition of IL-8 or SNAIL signaling appears to be beneficial for controlling colon and breast cancers [48]. Carcinopromoting role of M-CSF was confirmed, when disruption of M-CSF gene was found to cause diminished tumour growth and metastasis as a result of defective angiogenesis [49].…”
Section: Cytokines Regulate Cancer Stem Cells (Cscs)mentioning
confidence: 99%
“…SB-T-1214, one of the new-generation taxoids which was developed as an attempt to improve widely used taxane-based anticancer agents [62], has been demonstrated to induce growth inhibition and apoptotic cell death in drug resistant [63,64] and tumorigenic CD133+/CD44+ colon cancer spheroids [65], suggesting that this compound can specifically target tumor-specific SCLCs by inhibiting some stemness-related signaling pathways.…”
Section: Influence Of Sclcs In the Therapeutic Settingmentioning
confidence: 99%