HK2 Antibody, Biotin conjugated

1. downregulation of HK2 gene may be caused by its negative regulation through microRNAs miR-9-5p, -98-5p, and -199-5p. PMID:29695690
2. this study reports the structure of HK2 in complex with glucose and glucose-6-phosphate (G6P). PMID:29298880
3. Altogether, these findings provide strong support for the direct contribution of HK2 in B-cell lymphoma development and suggest that HK2 is a key metabolic driver of the diffuse large B-cell lymphoma phenotype. PMID:29335581
4. Taken together, these findings suggested that UCA1 may have an important role in regulating radioresistance through the HK2/glycolytic pathway, providing novel potential targets to improve cervical cancer RT. PMID:30015920
5. Data suggest that HK2 plays role in cisplatin resistance in ovarian cancer by regulating drug-induced, MAP kinase signaling-mediated autophagy. PMID:29247711
6. miR-125b-5p-HK2 pathway as a novel mechanism in regulating the glycolysis and progression of Laryngeal squamous cell carcinoma. PMID:29864898
7. These findings provide clues regarding the role of miR-216a-5p as a tumor suppressor in uveal melanoma through the inhibition of HK2. PMID:29763606
8. Overexpression of miR-125b inhibits cellular glucose metabolism through direct targeting of hexokinase 2. PMID:29631677
9. Data indicate that hexokinase-2 (HK2) was the direct target of miR-125b. PMID:29169422
10. Tesults suggest that mTOR-STAT3-HK2 pathway is involved in the glycolysis of HCC cells and STAT3 may regulate HCC glycolysis through HK2 pathway. PMID:28445971
11. our results demonstrate that deregulation of HK2 expression has an important function in the progression of TSCC and may serve as a biomarker of its metastatic potential in TSCC patients. HK2 enhances the metastatic potential of TSCC by stimulating the SOD2-H2O2 pathway. PMID:27926482
12. present studies highlight miR-143 as a tumor suppressor in oral squamous cell carcinoma (OSCC) by the suppression of cell migration, glucose metabolism and proliferation through directly targeting HK2, rendering miR-143 a therapeutic strategy for the treatment of clinical OSCC patients. PMID:28174335
13. FOXM1 bound directly to the GLUT1 and HK2 promoter regions and regulated the promoter activities and the expression of the genes at the transcriptional level. This reveals a novel mechanism by which glucose metabolism is regulated by FOXM1. PMID:27351131
14. our findings supported a mechanism whereby targeting HK2 inhibition contributed to suppress HPV16 E7-induced tumor glycolysis metabolism phenotype, inhibiting tumor growth, and induced apoptosis, blocking the cancer cell energy sources and ultimately enhanced the sensitivity of HPV(+) cervical cancer cells to irradiation therapy PMID:28498475
15. Data suggest Hexokinase 2 (HK2) as a potentially effective therapeutic target in Glioblastoma (GBM). PMID:27588472
16. High HKII expresiion is associated with nasopharyngeal carcinoma. PMID:26848773
17. Results show that the hexokinase 2 (HK2) promoter CpG island (HK2-CGI) surrounding regions N-shore was hypomethylated, thereby enhancing HK2 expression, the HK2-CGI was itself hypermethylated in some hepatocellular carcinomas (HCCs). PMID:27260001
18. findings confirmed the tumorigenic activity of HK2 in glioma, and the involvement of the miR218/Bmi1 pathway in the regulation of its expression PMID:29220380
19. BAG3 directly stabilizes hexokinase 2 mRNA and promotes aerobic glycolysis in pancreatic cancer cells. PMID:29114069
20. Previously unknown reciprocal influence of SIRT6 and HK2 in regulating autophagy driven monocyte differentiation. PMID:28935467
21. SIRT6 over-expression establishes a condition whereby reconfiguration of the Hexokinase 2 promoter chromatin structure makes it receptive to interaction with MZF1/SIRT6 complex, thereby favouring a regulatory state conducive to diminished transcription PMID:28478957
22. findings suggested that PVT1 contributes to osteosarcoma (OS) cell glucose metabolism, cell proliferation, and motility through the miR-497/HK2 pathway, and revealed a novel relation between lncRNA and the alteration of glycolysis in OS cells PMID:28602700
23. High HKII expression is associated with metastasis and epithelial-mesenchymal transition in hepatocellular carcinoma. PMID:28429188
24. The EML4-ALK-mediated upregulation of HIF1alpha, HK2 and glycolytic metabolism was also highly active in vivo as demonstrated by fluorodeoxyglucose-positron emission tomography imaging of xenografts grown from EML4-ALK-positive NSCLC cells. PMID:27132509
25. relevant number of patients with FDG-PET false-negative multiple myeloma and a strong association between hexokinase-2 expression and this negativity: a finding which may also be relevant for clinical imaging of other hematological cancers. PMID:28432222
26. MicroRNA-98 Suppress Warburg Effect by Targeting HK2 in Colon Cancer Cells. PMID:28025745
27. High HK2 expression is associated with prostate cancer. PMID:28098871
28. Metformin downregulated both endogenous and exogenous UCA1 expression, leading to the inhibition of mammalian target of rapamycin-signal transducer and activator of transcription 3-hexokinase 2 signaling pathway. Our study provided the first evidence that metformin inhibited proliferation and glycolysis in cancer cells through regulation of long non-coding RNA UCA1 PMID:28641488
29. AKT inhibition blocks miR-124 silencing-induced AKT1/2, glucose transporter 1, hexokinase II activation, cell proliferation, and glycolytic or energy metabolism changes. In summary, this study demonstrated that miR-124 is able to inhibit proliferation, glycolysis, and energy metabolism, potentially by targeting AKT1/2-glucose transporter 1/hexokinase II in non-small cell lung cancer cells. PMID:28488541
30. Results from the simulations show that HK2 binding restricts the movement of the VDAC1 N-terminal helix. As a result, VDAC1 is kept in the open state most of the time and probably allows a constant supply of ATP to HK2 for glycolysis. PMID:27544294
31. These results suggest that HK2 plays important roles in the glycolytic, proliferation and migration properties of colorectal carcinoma PMID:27363977
32. HK2modulated glucose metabolism was significantly upregulated by overexpression of miR155. Notably, inhibition of miR155 sensitized lung cancer cells to irradiation via suppression of glucose metabolism. PMID:27315591
33. We demonstrated that the expression levels of glycolysis-related proteins glucose transporter 1, hexokinase II, carbonic anhydrase IX, and monocarbonylate transporter 4 differ between thyroid cancer subtypes and are correlated with poorer prognosis PMID:28347233
34. miR-181b directly inhibits the expression level of hexokinase 2 (HK2), a key enzyme that catalyzes the first step of glycolysis, through targeting its 3'-untranslated region. PMID:27314295
35. The N-terminal end of HKII has a mitochondrial-binding site and a VDAC bindig site. PMID:26182367
36. HK2 functions as a novel oncogene in lung cancer and may be a potential therapeutic target for lung cancer. PMID:26802651
37. Cells with HKII knockdown showed no changes in 3BP sensitivity, suggesting the effects of 3BP are independent of HKII expression. PMID:26740252
38. Suggest HK2 as an independent prognostic indicator of radiation resistance in cervical squamous carcinoma. PMID:26097593
39. High exokinase 2 expression is associated with neuroblastoma metastasis. PMID:26986252
40. The degree of plaque disruption and expression of TF and HK-II appear to be important vascular factors for AMI onset, and polarized macrophages make a distinct contribution to thrombogenicity and glucose metabolism. PMID:26346032
41. The overexpression of Hk2 (and Pkm2) sustains high levels of glycolysis during embryonic stem cell differentiation. PMID:26059508
42. In the present study it was determined whether three key enzymes for glycolysis, glutaminolysis and de novo synthesis of FAs, hexokinase-2, glutaminase and fatty acid synthase PMID:26134042
43. In conclusion, our findings suggested that miR-4458 inhibited the progression of colon cancer cells by inhibition of glycolysis and lactate production via directly targeting HK2 mRNA. PMID:26607110
44. Hexokinase 2 controls cellular stress response through localization of hnRNP A1. PMID:26247723
45. Insulin resistance in obese boys leads to up-regulation of INSIG2 gene expression as well as to down-regulation of PFKFB1, PFKFB3, and HK2 genes in the blood cells as compared to obese patients with normal insulin sensitivity. PMID:26827442
46. HK2 was identified as a chaperone-mediated autophagy substrate. PMID:26323688
47. study reveals a novel relationship between PI3K/Akt signaling and aerobic glycolysis and indicates that PI3K/Akt/HK2 might be potential therapeutic approaches for OS PMID:26116768
48. HK2 regulated the protein level and T14 phosphorylation of CDK2, and knockdown of HK2 resulted in a G1 phase cell cycle arrest. PMID:24780297
49. High HK-II expression was correlated with esophageal adenocarcinoma compared with squamous cell carcinoma. PMID:24939624
50. Suggest that upregulation of HKII occurs during the process of hepatocarcinogenesis in humans. PMID:25381201

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HGNC: 4923

UNIGENE: Hs.406266

KEGG: hsa:3099

STRING: 9606.ENSP00000290573

OMIM: 601125