Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In mouse models of melanoma, the combinatorial regimen of using the PLGA nanoparticles with the CXCL1 hydrogels exhibited superior tumor inhibition capability.
|
31818156 |
2020 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Increased tumor (nuclear) TNFα and IL-1β, CX3CL1 and CXCL1 gene expression was observed in the WLI.Tumor Ki67 did not differ between arms.
|
31442303 |
2020 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Systemic administration of HL2401 in mice bearing bladder and prostate xenograft tumors retarded tumor growth through the inhibition of cellular proliferation and angiogenesis along with an induction of apoptosis.
|
30809313 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
(2018) generate a library of clonal PDAC tumors to examine the tumor-intrinsic features shaping the anti-tumor immune response and find that tumor cell-derived CXCL1 directly blunts T cell infiltration and reduces responsiveness to immunotherapy.
|
30021140 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Cxcl1 KD phenocopied the effects of Plac1 KD on tumor growth, and overexpression of Cxcl1 partially rescued Plac1 KD cells.
|
29632317 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
CXCL1 expression was correlated with tumor diameter (<i>P</i>=0.002), T stage (<i>P</i>=0.044), N stage (<i>P</i>=0.005), M stage (<i>P</i>=0.001), lymphovascular invasion (<i>P</i>=0.010), and carcinoembryonic antigen status (<i>P</i>=0.019).
|
29784873 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Metformin inhibited CXCL1 secretion in ESCC cells and tumor xenografts by enhancing AMPK phosphorylation and inducing DACH1 expression, leading to NF-κB inhibition and reducing MDSC migration.
|
29900050 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Snail knockdown reduces the expression of CXCR2 ligands (CXCL1 and CXCL2), chemokines that attract MDSCs to the tumor via CXCR2.
|
29703902 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Together, our study highlighted CAF-secreted CXCL1 as an attractive target to reverse tumor radioresistance and can be used as an independent prognostic factor of ESCC patients treated with chemoradiotherapy.
|
28518141 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Melanomas developed from cells lacking MyD88 showed an enhanced secretion of chemoattractant ligands such as CCL2, CXCL10 and CXCL1 and have an improved infiltration of macrophages to the tumor site.
|
28662055 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Clinicopathologic significance of the CXCL1-CXCR2 axis in the tumor microenvironment of gastric carcinoma.
|
28575019 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Here, we successfully isolated tumor-associated LECs (T-LECs) and normal LECs (N-LECs) from clinical samples by magnetic-activated cell sorting system (MACS) and proved that CXCL1 expression was elevated in T-LECs compared with N-LECs in situ and vitro.
|
27832972 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Here, we demonstrate that colorectal carcinoma cells secrete VEGFA, which stimulates tumor-associated macrophages to produce CXCL1 in the primary tumor.
|
28455419 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Analysis of immune cells revealed that CXCR2 ligands (CXCL1, CXCL 2 and CXCL5) expressed by TNFα-activated MSCs efficiently recruited CXCR2<sup>+</sup> neutrophils into tumor.
|
27375023 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In addition, an experiment using the orthotopic bladder cancer model revealed that CXCL1 production in TAMs/CAFs supported tumor implantation into the murine bladder wall and UCB growth when injected together, which was confirmed by clinical data of patients with bladder cancer.
|
27690238 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The mbIL-12-mediated decrease in tumor burden was associated with a significant reduction in neutrophil and macrophage infiltration in the OFB, and correlated with a reduced expression of neutrophil and macrophage chemoattractants (CXCL1, -2, -3 and CCL2, -7).
|
26430781 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
High GRO-α expression in the cytoplasm of cancer cells was related to tumor location (P = 0.047), tumor status (T classification; P = 0.001), distant metastasis (P < 0.001), and tumor node metastasis (TNM) stage (P < 0.001).
|
27472713 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
CXCL1 protein expression was detected by IHC in 41 patients (41%), these were associated with advanced tumor‑node‑metastasis (TNM) stage, LMVD, tumor differentiation and poor survival.
|
27748927 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, knocking down CXCL1 expression in 3LL cells significantly hindered tumor growth by inhibiting recruitment of neutrophils from peripheral blood into tumor tissues.
|
27446967 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Using mouse models, we show that the CXCL1 chemokine gradient is required for the obesity-dependent tumour ASC recruitment, vascularization and tumour growth promotion.
|
27241286 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Taken together, our results indicate that adiponectin promotes stromal cell senescence within invasive colon cancer contributing to angiogenesis and tumor growth in part through the production of CXCL1 and may serve as a therapeutic target for tumor patients.
|
27092462 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
CBRH-7919 cells carrying CXCL1 siRNA resulted in decreased tumor growth in nude mice.
|
27682863 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
CXCL1 from DGC cells stimulates the recruitment of BM-MCs into tumor stroma via CXCR2 signaling of BM-MCs.
|
27742059 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In situ hybridization could confirm the upregulation of CXCL1 and downregulation of CA7 in colorectal adenomas and tumors compared to healthy controls.
|
26208990 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Upon γ-irradiation of glioma cells, IκBζ expression is enhanced, and subsequently serves as a transcriptional activator of the tumor promoting cytokines interleukin (IL-6), IL-8 and chemokine (C-X-C motif) ligand 1 (CXCL1) that are known to be involved in glioma associated inflammatory processes.
|
26398661 |
2015 |