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HKDC1 upregulation promotes glycolysis and disease progression, and confers chemoresistance onto gastric cancer
by
Xu, Hui‐Wen
, Ma, Yuan‐Zhen
, Zhu, Sen‐Lin
, Suo, Da‐Qin
, Guan, Xin‐Yuan
, Li, Yan
, Zhan, Jia‐Rong
, Wang, Mei‐Qian
, Chen, Yi‐Ru
, Wang, Ji‐Jin
in
5-Fluorouracil
/ Antigens
/ Carcinogenesis - genetics
/ Cell Line, Tumor
/ Cell migration
/ Cell Movement - genetics
/ Cell Proliferation
/ Chemoresistance
/ Chemotherapy
/ Cisplatin
/ Clinical significance
/ Confidence intervals
/ Disease
/ Disease Progression
/ DNA damage
/ DNA repair
/ Drug resistance
/ Drug Resistance, Neoplasm - genetics
/ Epithelial-Mesenchymal Transition - genetics
/ Fluorouracil - pharmacology
/ Gastric cancer
/ Gene expression
/ Gene Expression Regulation, Neoplastic
/ Genomes
/ Glucose
/ Glycolysis
/ Hexokinase
/ Hexokinase - genetics
/ Hexokinase - metabolism
/ HKDC1
/ Humans
/ Immunohistochemistry
/ Kinases
/ Medical prognosis
/ Metabolism
/ Metastases
/ Metastasis
/ NF-kappa B - metabolism
/ NF-κB protein
/ Original
/ Oxaliplatin
/ Polymerase chain reaction
/ Proteins
/ Stomach Neoplasms - drug therapy
/ Stomach Neoplasms - genetics
/ Stomach Neoplasms - metabolism
/ Tumorigenesis
/ Tumors
/ Up-Regulation
2023
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HKDC1 upregulation promotes glycolysis and disease progression, and confers chemoresistance onto gastric cancer
by
Xu, Hui‐Wen
, Ma, Yuan‐Zhen
, Zhu, Sen‐Lin
, Suo, Da‐Qin
, Guan, Xin‐Yuan
, Li, Yan
, Zhan, Jia‐Rong
, Wang, Mei‐Qian
, Chen, Yi‐Ru
, Wang, Ji‐Jin
in
5-Fluorouracil
/ Antigens
/ Carcinogenesis - genetics
/ Cell Line, Tumor
/ Cell migration
/ Cell Movement - genetics
/ Cell Proliferation
/ Chemoresistance
/ Chemotherapy
/ Cisplatin
/ Clinical significance
/ Confidence intervals
/ Disease
/ Disease Progression
/ DNA damage
/ DNA repair
/ Drug resistance
/ Drug Resistance, Neoplasm - genetics
/ Epithelial-Mesenchymal Transition - genetics
/ Fluorouracil - pharmacology
/ Gastric cancer
/ Gene expression
/ Gene Expression Regulation, Neoplastic
/ Genomes
/ Glucose
/ Glycolysis
/ Hexokinase
/ Hexokinase - genetics
/ Hexokinase - metabolism
/ HKDC1
/ Humans
/ Immunohistochemistry
/ Kinases
/ Medical prognosis
/ Metabolism
/ Metastases
/ Metastasis
/ NF-kappa B - metabolism
/ NF-κB protein
/ Original
/ Oxaliplatin
/ Polymerase chain reaction
/ Proteins
/ Stomach Neoplasms - drug therapy
/ Stomach Neoplasms - genetics
/ Stomach Neoplasms - metabolism
/ Tumorigenesis
/ Tumors
/ Up-Regulation
2023
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HKDC1 upregulation promotes glycolysis and disease progression, and confers chemoresistance onto gastric cancer
by
Xu, Hui‐Wen
, Ma, Yuan‐Zhen
, Zhu, Sen‐Lin
, Suo, Da‐Qin
, Guan, Xin‐Yuan
, Li, Yan
, Zhan, Jia‐Rong
, Wang, Mei‐Qian
, Chen, Yi‐Ru
, Wang, Ji‐Jin
in
5-Fluorouracil
/ Antigens
/ Carcinogenesis - genetics
/ Cell Line, Tumor
/ Cell migration
/ Cell Movement - genetics
/ Cell Proliferation
/ Chemoresistance
/ Chemotherapy
/ Cisplatin
/ Clinical significance
/ Confidence intervals
/ Disease
/ Disease Progression
/ DNA damage
/ DNA repair
/ Drug resistance
/ Drug Resistance, Neoplasm - genetics
/ Epithelial-Mesenchymal Transition - genetics
/ Fluorouracil - pharmacology
/ Gastric cancer
/ Gene expression
/ Gene Expression Regulation, Neoplastic
/ Genomes
/ Glucose
/ Glycolysis
/ Hexokinase
/ Hexokinase - genetics
/ Hexokinase - metabolism
/ HKDC1
/ Humans
/ Immunohistochemistry
/ Kinases
/ Medical prognosis
/ Metabolism
/ Metastases
/ Metastasis
/ NF-kappa B - metabolism
/ NF-κB protein
/ Original
/ Oxaliplatin
/ Polymerase chain reaction
/ Proteins
/ Stomach Neoplasms - drug therapy
/ Stomach Neoplasms - genetics
/ Stomach Neoplasms - metabolism
/ Tumorigenesis
/ Tumors
/ Up-Regulation
2023
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HKDC1 upregulation promotes glycolysis and disease progression, and confers chemoresistance onto gastric cancer
Journal Article
HKDC1 upregulation promotes glycolysis and disease progression, and confers chemoresistance onto gastric cancer
2023
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Overview
There is increasing evidence that hexokinase is involved in cell proliferation and migration. However, the function of the hexokinase domain containing protein‐1 (HKDC1) in gastric cancer (GC) remains unclear. Immunohistochemistry analysis and big data mining were used to evaluate the correlation between HKDC1 expression and clinical features in GC. In addition, the biological function and molecular mechanism of HKDC1 in GC were studied by in vitro and in vivo assays. Our study indicated that HKDC1 expression was upregulated in GC tissues compared with adjacent nontumor tissues. High expression of HKDC1 was associated with worse prognosis. Functional experiments demonstrated that HKDC1 upregulation promoted glycolysis, cell proliferation, and tumorigenesis. In addition, HKDC1 could enhance GC invasion and metastasis by inducing epithelial–mesenchymal transition (EMT). Abrogation of HKDC1 could effectively attenuate its oncogenic and metastatic function. Moreover, HKDC1 promoted GC proliferation and migration in vivo. HKDC1 overexpression conferred chemoresistance to cisplatin, oxaliplatin, and 5‐fluorouracil (5‐Fu) onto GC cells. Furthermore, nuclear factor kappa‐B (NF‐κB) inhibitor PS‐341 could attenuate tumorigenesis, metastasis, and drug resistance ability induced by HKDC1 overexpression in GC cells. Our results highlight a critical role of HKDC1 in promoting glycolysis, tumorigenesis, and EMT of GC cells via activating the NF‐κB pathway. In addition, HKDC1‐mediated drug resistance was associated with DNA damage repair, which further activated NF‐κB signaling. HKDC1 upregulation may be used as a potential indicator for choosing an effective chemotherapy regimen for GC patients undergoing chemotherapy. HKDC1 upregulation predicts resistance to cisplatin, oxaliplatin and 5‐FU in patients with GC. HKDC1 upregulation may be used as a potential indicator for choosing an effective chemotherapy regimen for GC patients undergoing chemotherapy.
Publisher
John Wiley & Sons, Inc,John Wiley and Sons Inc
Subject
/ Antigens
/ Disease
/ Drug Resistance, Neoplasm - genetics
/ Epithelial-Mesenchymal Transition - genetics
/ Gene Expression Regulation, Neoplastic
/ Genomes
/ Glucose
/ HKDC1
/ Humans
/ Kinases
/ Original
/ Proteins
/ Stomach Neoplasms - drug therapy
/ Stomach Neoplasms - genetics
/ Stomach Neoplasms - metabolism
/ Tumors
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