2016
DOI: 10.1371/journal.pone.0167857
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Downregulation of FBP1 Promotes Tumor Metastasis and Indicates Poor Prognosis in Gastric Cancer via Regulating Epithelial-Mesenchymal Transition

Abstract: BackgroundRecent studies indicated that some glycolytic enzymes are complicated, multifaceted proteins rather than simple components of the glycolytic pathway. FBP1 plays a vital role in glucose metabolism, but its role in gastric cancer tumorigenesis and metastasis has not been fully understood.MethodsThe prognostic value of FBP1 was first studied in The Cancer Genome Atlas (TCGA) database and validated in in-house database. The effect of FBP1 on cell proliferation and metastasis was examined in vitro. Nonpar… Show more

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Cited by 66 publications
(93 citation statements)
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“…The characteristics of the samples are shown in Table 1. Construction of the TMA was performed as described previously [8].…”
Section: Patients and Samplesmentioning
confidence: 99%
“…The characteristics of the samples are shown in Table 1. Construction of the TMA was performed as described previously [8].…”
Section: Patients and Samplesmentioning
confidence: 99%
“…Construction of the TMA and IHC staining were performed as described previously (9,10). Gas1 and FOXM1 anti-human rabbit polyclonal antibodies were used at a dilution of 1:100 (AP11869a; Abgent) and 1:50 (sr-500; Santa Cruz Biotechnology), respectively; PBS was used alternately as negative control.…”
Section: Construction Of the Tma And Ihc Stainingmentioning
confidence: 99%
“…Cell proliferation was assessed by CCK8 assay as described previously (10). To determine clonogenic ability, 200 cells were transplanted in each well of a 6-well dish and allowed to grow for 14 days to form colonies.…”
Section: Cell Proliferation and Clonogenic Assaymentioning
confidence: 99%
See 1 more Smart Citation
“…We have proved that FOXC-2 over expression was related to aggressive molecular subtype particularly triple negative breast carcinomas (TNBCs) that was in line with results of Hollier et al [13], who found that FOXC2 levels were up-regulated in triple negative breast carcinoma and also up-regulated in the to induce the expression of several cell cycle regulators, including cyclin-dependent kinase 1 (CDK1), suggesting a role for FOXC2 phosphorylation in the expression of cell cycle-specific genes and that FOXC2 may regulate the cell cycle in CSC-rich cell populations [18], that subsequently might increased proliferation in plethora of cancer types [19] [20] [21].…”
Section: Discussionmentioning
confidence: 99%