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CPEB3 inhibits epithelial-mesenchymal transition by disrupting the crosstalk between colorectal cancer cells and tumor-associated macrophages via IL-6R/STAT3 signaling
by
He, Chengcheng
, Lai, Qiuhua
, Yan, Qun
, Li, Aimin
, Liu, Side
, Zhong, Qian
, Wang, Shanci
, Fang, Yuxin
in
Animals
/ Antibodies
/ Apoptosis
/ Biochemistry
/ Biomarkers, Tumor - genetics
/ Biomarkers, Tumor - metabolism
/ Biomedical and Life Sciences
/ Biomedicine
/ Cancer cells
/ Cancer Research
/ Cell cycle
/ Cell Proliferation
/ Colorectal cancer
/ Colorectal Neoplasms - genetics
/ Colorectal Neoplasms - metabolism
/ Colorectal Neoplasms - pathology
/ CPEB3
/ Cytokines
/ Cytoplasmic polyadenylation element binding protein 3
/ Development and progression
/ EMT
/ Epithelial-Mesenchymal Transition
/ Extracellular matrix
/ Flow cytometry
/ Gene Expression Regulation, Neoplastic
/ Humans
/ IL-6
/ Immunology
/ Kinases
/ Laboratory animals
/ Macrophages
/ Male
/ Mice
/ Mice, Inbred BALB C
/ Mice, Nude
/ Oncology
/ Pathogens
/ Prognosis
/ Protein binding
/ Protein expression
/ Proteins
/ Receptors, Interleukin-6 - genetics
/ Receptors, Interleukin-6 - metabolism
/ RNA
/ RNA-Binding Proteins - genetics
/ RNA-Binding Proteins - metabolism
/ Signal transduction
/ STAT3 Transcription Factor - genetics
/ STAT3 Transcription Factor - metabolism
/ Stem cells
/ Tumor Cells, Cultured
/ Tumor Microenvironment
/ Tumor-associated macrophage
/ Tumor-Associated Macrophages - metabolism
/ Tumor-Associated Macrophages - pathology
/ Tumors
/ Xenograft Model Antitumor Assays
2020
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CPEB3 inhibits epithelial-mesenchymal transition by disrupting the crosstalk between colorectal cancer cells and tumor-associated macrophages via IL-6R/STAT3 signaling
by
He, Chengcheng
, Lai, Qiuhua
, Yan, Qun
, Li, Aimin
, Liu, Side
, Zhong, Qian
, Wang, Shanci
, Fang, Yuxin
in
Animals
/ Antibodies
/ Apoptosis
/ Biochemistry
/ Biomarkers, Tumor - genetics
/ Biomarkers, Tumor - metabolism
/ Biomedical and Life Sciences
/ Biomedicine
/ Cancer cells
/ Cancer Research
/ Cell cycle
/ Cell Proliferation
/ Colorectal cancer
/ Colorectal Neoplasms - genetics
/ Colorectal Neoplasms - metabolism
/ Colorectal Neoplasms - pathology
/ CPEB3
/ Cytokines
/ Cytoplasmic polyadenylation element binding protein 3
/ Development and progression
/ EMT
/ Epithelial-Mesenchymal Transition
/ Extracellular matrix
/ Flow cytometry
/ Gene Expression Regulation, Neoplastic
/ Humans
/ IL-6
/ Immunology
/ Kinases
/ Laboratory animals
/ Macrophages
/ Male
/ Mice
/ Mice, Inbred BALB C
/ Mice, Nude
/ Oncology
/ Pathogens
/ Prognosis
/ Protein binding
/ Protein expression
/ Proteins
/ Receptors, Interleukin-6 - genetics
/ Receptors, Interleukin-6 - metabolism
/ RNA
/ RNA-Binding Proteins - genetics
/ RNA-Binding Proteins - metabolism
/ Signal transduction
/ STAT3 Transcription Factor - genetics
/ STAT3 Transcription Factor - metabolism
/ Stem cells
/ Tumor Cells, Cultured
/ Tumor Microenvironment
/ Tumor-associated macrophage
/ Tumor-Associated Macrophages - metabolism
/ Tumor-Associated Macrophages - pathology
/ Tumors
/ Xenograft Model Antitumor Assays
2020
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CPEB3 inhibits epithelial-mesenchymal transition by disrupting the crosstalk between colorectal cancer cells and tumor-associated macrophages via IL-6R/STAT3 signaling
by
He, Chengcheng
, Lai, Qiuhua
, Yan, Qun
, Li, Aimin
, Liu, Side
, Zhong, Qian
, Wang, Shanci
, Fang, Yuxin
in
Animals
/ Antibodies
/ Apoptosis
/ Biochemistry
/ Biomarkers, Tumor - genetics
/ Biomarkers, Tumor - metabolism
/ Biomedical and Life Sciences
/ Biomedicine
/ Cancer cells
/ Cancer Research
/ Cell cycle
/ Cell Proliferation
/ Colorectal cancer
/ Colorectal Neoplasms - genetics
/ Colorectal Neoplasms - metabolism
/ Colorectal Neoplasms - pathology
/ CPEB3
/ Cytokines
/ Cytoplasmic polyadenylation element binding protein 3
/ Development and progression
/ EMT
/ Epithelial-Mesenchymal Transition
/ Extracellular matrix
/ Flow cytometry
/ Gene Expression Regulation, Neoplastic
/ Humans
/ IL-6
/ Immunology
/ Kinases
/ Laboratory animals
/ Macrophages
/ Male
/ Mice
/ Mice, Inbred BALB C
/ Mice, Nude
/ Oncology
/ Pathogens
/ Prognosis
/ Protein binding
/ Protein expression
/ Proteins
/ Receptors, Interleukin-6 - genetics
/ Receptors, Interleukin-6 - metabolism
/ RNA
/ RNA-Binding Proteins - genetics
/ RNA-Binding Proteins - metabolism
/ Signal transduction
/ STAT3 Transcription Factor - genetics
/ STAT3 Transcription Factor - metabolism
/ Stem cells
/ Tumor Cells, Cultured
/ Tumor Microenvironment
/ Tumor-associated macrophage
/ Tumor-Associated Macrophages - metabolism
/ Tumor-Associated Macrophages - pathology
/ Tumors
/ Xenograft Model Antitumor Assays
2020
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CPEB3 inhibits epithelial-mesenchymal transition by disrupting the crosstalk between colorectal cancer cells and tumor-associated macrophages via IL-6R/STAT3 signaling
Journal Article
CPEB3 inhibits epithelial-mesenchymal transition by disrupting the crosstalk between colorectal cancer cells and tumor-associated macrophages via IL-6R/STAT3 signaling
2020
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Overview
Background
Crosstalk between cancer cells and tumor-associated macrophages (TAMs) mediates tumor progression in colorectal cancer (CRC). Cytoplasmic polyadenylation element binding protein 3 (CPEB3) has been shown to exhibit tumor-suppressive role in CRC.
Methods
The expression of CPEB3, CD68, CD86 and CD163 was determined in CRC tissues. SW480 or HCT116 cells overexpressing CPEB3 and LoVo or RKO cells with CPEB3 knockdown were constructed. Stably transfected CRC cells were co-cultured with THP-1 macrophages to determine the malignant phenotype of CRC cells, macrophage polarization, and secretory signals. The inhibition of CPEB3 on tumor progression and M2-like TAM polarization was confirmed in nude mice.
Results
Decreased CPEB3 expression in CRC was associated with fewer CD86
+
TAMs and more CD163
+
TAMs. CPEB3 knockdown in CRC cells increased the number of CD163
+
TAMs and the expression of IL1RA, IL-6, IL-4 and IL-10 in TAM supernatants. TAMs enhanced CRC cell proliferation and invasion via IL-6, and then activated the IL-6R/STAT3 pathway in CRC cells. However, CPEB3 reduced the IL-6R protein levels by directly binding to IL-6R mRNA, leading to decreased phosphorylated-STAT3 expression in CRC cells. CCL2 was significantly increased in CPEB3 knockdown cells, while CCL2 antibody treatment rescued the effect of CPEB3 knockdown in promoting CD163
+
TAM polarization. Eventually, we confirmed that CPEB3 inhibits tumor progression and M2-like TAM polarization in vivo.
Conclusions
CPEB3 is involved in the crosstalk between CRC cells and TAMs by targeting IL-6R/STAT3 signaling.
Publisher
BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
Subject
/ Biomarkers, Tumor - genetics
/ Biomarkers, Tumor - metabolism
/ Biomedical and Life Sciences
/ Colorectal Neoplasms - genetics
/ Colorectal Neoplasms - metabolism
/ Colorectal Neoplasms - pathology
/ CPEB3
/ Cytoplasmic polyadenylation element binding protein 3
/ EMT
/ Epithelial-Mesenchymal Transition
/ Gene Expression Regulation, Neoplastic
/ Humans
/ IL-6
/ Kinases
/ Male
/ Mice
/ Oncology
/ Proteins
/ Receptors, Interleukin-6 - genetics
/ Receptors, Interleukin-6 - metabolism
/ RNA
/ RNA-Binding Proteins - genetics
/ RNA-Binding Proteins - metabolism
/ STAT3 Transcription Factor - genetics
/ STAT3 Transcription Factor - metabolism
/ Tumor-Associated Macrophages - metabolism
/ Tumor-Associated Macrophages - pathology
/ Tumors
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