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⇱ The chemokine MCP-1 (CCL2) in the host interaction with cancer: a foe or ally?


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2018
DOI: 10.1038/cmi.2017.135 |Get access via publisher |Summarize |
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The chemokine MCP-1 (CCL2) in the host interaction with cancer: a foe or ally?

Abstract: Macrophages are one of the most abundant leukocyte populations infiltrating tumor tissues and can exhibit both tumoricidal and tumor-promoting activities. In 1989, we reported the purification of monocyte chemoattractant protein-1 (MCP-1) from culture supernatants of mitogen-activated peripheral blood mononuclear cells and tumor cells. MCP-1 is a potent monocyte-attracting chemokine, identical to the previously described lymphocyte-derived chemotactic factor or tumor-derived chemotactic factor, and greatly con… Show more

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Cited by 267 publications

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β€œβ€¦10b ). These findings suggest that the major cell types recruited by ORM2 injection are monocytes/macrophages, in accordance with the in vitro findings that ORM2 increases the CCL2 production necessary for monocyte recruitment 34 , in contrast with the finding that ORM2 has no effect on CXCL8 production for neutrophil recruitment 35 .
Fig.
…”
Section: Resultssupporting
confidence: 88%
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD). Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD. The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC). Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
β€œβ€¦10b ). These findings suggest that the major cell types recruited by ORM2 injection are monocytes/macrophages, in accordance with the in vitro findings that ORM2 increases the CCL2 production necessary for monocyte recruitment 34 , in contrast with the finding that ORM2 has no effect on CXCL8 production for neutrophil recruitment 35 .
Fig.
…”
Section: Resultssupporting
confidence: 88%
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD). Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD. The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC). Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
β€œβ€¦might promote intestinal lumen inflammation and induce the CCL2 transcription by cells in the tumor microenvironment. In support of our hypothesis, recent findings link CCL2 to the inflammation and cancer pathogenesis and provide evidence that CCL2 production in tumors is due to complex interactions between tumor and non-tumor cells, both cells contributing to the high tumor-associated CCL2 levels [ 10 , 11 ]. However, we cannot rule out that other potential confounders covariates could contribute in increasing CCL2 levels in CRC and further studies should confirm our results.…”
Section: Discussionsupporting
confidence: 81%
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD). Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD. The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC). Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
β€œβ€¦A high expression of CCL2 in the tumors was shown to correlate with a poor prognosis [19,20]. We found a fraction of stromal lymphocytes also expressing CCL2, which is in accordance with previous reports of CCL2 being produced not only by tumor cells themselves but also by stromal cells in response to various inflammatory stimuli [21][22][23][24]. We found the number of highly CCL2 positive cancer cells higher in the CNBs, while the fraction of CCL2-positive lymphocytes was significantly higher in post-biopsy resected tumors.…”
Section: Expression Of Ccl2supporting
confidence: 91%
Exaggerated anticipatory anxiety is common in social anxiety disorder (SAD). Neuroimaging studies have revealed altered neural activity in response to social stimuli in SAD, but fewer studies have examined neural activity during anticipation of feared social stimuli in SAD. The current study examined the time course and magnitude of activity in threat processing brain regions during speech anticipation in socially anxious individuals and healthy controls (HC). Method Participants (SAD n = 58; HC n = 16) underwent functional magnetic resonance imaging (fMRI) during which they completed a 90s control anticipation task and 90s speech anticipation task.
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