Grp78 promotes the invasion of hepatocellular carcinoma.
about
Melanoma and the Unfolded Protein ResponseGlucose-regulated protein 78 demonstrates antiviral effects but is more suitable for hepatocellular carcinoma prevention in hepatitis B.Lack of association between the GRP78 polymorphisms in the promoter and 3' UTR and susceptibility to chronic HBV infection in a Chinese Han population.Antitumor agent 25-epi Ritterostatin GN1N induces endoplasmic reticulum stress and autophagy mediated cell death in melanoma cellsGranulin-epithelin precursor interacts with 78-kDa glucose-regulated protein in hepatocellular carcinomaLyGDI, a novel SHIP-interacting protein, is a negative regulator of FcγR-mediated phagocytosis.Endoplasmic reticulum stress and cancer.Glucose regulated protein 78 promotes cell invasion via regulation of uPA production and secretion in colon cancer cells.Clusterin protects hepatocellular carcinoma cells from endoplasmic reticulum stress induced apoptosis through GRP78.Proteomic differences between hepatocellular carcinoma and nontumorous liver tissue investigated by a combined gel-based and label-free quantitative proteomics study.The 3' UTR variants in the GRP78 are not associated with overall survival in resectable hepatocellular carcinoma.De-acetylation and degradation of HSPA5 is critical for E1A metastasis suppression in breast cancer cells.Endoplasmic reticulum stress in endometrial cancer.Autoantibodies against cell surface GRP78 promote tumor growth in a murine model of melanomaRole of prostate apoptosis response 4 in translocation of GRP78 from the endoplasmic reticulum to the cell surface of trophoblastic cells.JNK contributes to the tumorigenic potential of human cholangiocarcinoma cells through the mTOR pathway regulated GRP78 induction.Upregulation of heat shock proteins (HSPA12A, HSP90B1, HSPA4, HSPA5 and HSPA6) in tumour tissues is associated with poor outcomes from HBV-related early-stage hepatocellular carcinoma.Unfolding the Role of Stress Response Signaling in Endocrine Resistant Breast Cancers.Melatonin Activates Endoplasmic Reticulum Stress and Apoptosis in Rats with Diethylnitrosamine-Induced HepatocarcinogenesisElevated GRP78 expression is associated with poor prognosis in patients with pancreatic cancer3'3-Diindolylmethane inhibits migration, invasion and metastasis of hepatocellular carcinoma by suppressing FAK signaling.GRP78 confers the resistance to 5-FU by activating the c-Src/LSF/TS axis in hepatocellular carcinomaAutoantibodies against glucose-regulated protein 78 as serological diagnostic biomarkers in hepatocellular carcinomaThe cell surface GRP78 facilitates the invasion of hepatocellular carcinoma cells.High expression of glucose-regulated protein 78 (GRP78) is associated with metastasis and poor prognosis in patients with esophageal squamous cell carcinoma.GRP78 as a regulator of liver steatosis and cancer progression mediated by loss of the tumor suppressor PTEN.The biological and therapeutic relevance of mRNA translation in cancer.Targeting GRP78 and antiestrogen resistance in breast cancer.Expression of ER stress and autophagy-related molecules in human non-small cell lung cancer and premalignant lesions.Oncolytic vaccinia virus inhibits human hepatocellular carcinoma MHCC97-H cell proliferation via endoplasmic reticulum stress, autophagy and Wnt pathways.Grp78 Is Critical for Amelogenin-Induced Cell Migration in a Multipotent Clonal Human Periodontal Ligament Cell Line.High Expression of GRP78 Promotes Invasion and Metastases in Patients with Esophageal Squamous Cell Carcinoma.Nanoparticles inhibit cancer cell invasion and enhance antitumor efficiency by targeted drug delivery via cell surface-related GRP78.GRP78 promotes the invasion of pancreatic cancer cells by FAK and JNK.Knockdown of glucose-regulated protein 78 decreases the invasion, metalloproteinase expression and ECM degradation in hepatocellular carcinoma cells.Silencing of glucose-regulated protein 78 (GRP78) enhances cell migration through the upregulation of vimentin in hepatocellular carcinoma cells.Glucose-regulated protein 58 modulates cell invasiveness and serves as a prognostic marker for cervical cancer.Secreted GRP78 activates EGFR-SRC-STAT3 signaling and confers the resistance to sorafeinib in HCC cells.Deficiency of protein-L-isoaspartate (D-aspartate) O-methyl-transferase expression under endoplasmic reticulum stress promotes epithelial mesenchymal transition in lung adenocarcinoma.Mouse models for investigating the underlying mechanisms of nonalcoholic steatohepatitis-derived hepatocellular carcinoma.
P2860
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P2860
Grp78 promotes the invasion of hepatocellular carcinoma.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Grp78 promotes the invasion of hepatocellular carcinoma.
@ast
Grp78 promotes the invasion of hepatocellular carcinoma.
@en
Grp78 promotes the invasion of hepatocellular carcinoma.
@nl
type
label
Grp78 promotes the invasion of hepatocellular carcinoma.
@ast
Grp78 promotes the invasion of hepatocellular carcinoma.
@en
Grp78 promotes the invasion of hepatocellular carcinoma.
@nl
prefLabel
Grp78 promotes the invasion of hepatocellular carcinoma.
@ast
Grp78 promotes the invasion of hepatocellular carcinoma.
@en
Grp78 promotes the invasion of hepatocellular carcinoma.
@nl
P2093
P2860
P356
P1433
P1476
Grp78 promotes the invasion of hepatocellular carcinoma.
@en
P2093
Cuifen Bao
Hongdan Li
Huijuan Song
Liufang Cheng
Rongjian Su
P2860
P2888
P356
10.1186/1471-2407-10-20
P407
P577
2010-01-19T00:00:00Z
P5875
P6179
1046991698