Table 4.
VTE related-genes reported by GWAS and their putative links with cancer hallmarks.
| Genes | HUGO nomenclature | Molecular processes that promote carcinogenesis | Potential cancer hallmarks |
|---|---|---|---|
| F5 | Coagulation Factor V | Generation of thrombin | Metastasis, angiogenesis, immune evasion and apoptosis [11] |
| CCDC181 (C1orf114) | Coiled-Coil Domain Containing 181 | Despite the unknown role in carcinogenesis, this gene is frequently methylated in patients with prostate cancer [12] | Genome instability and mutation |
| ABO | ABO Blood Group | Activation of adhesion molecules [13] | Inflammation, immune evasion and metastasis [13, 14] |
| Regulation of plasmatic levels of von Willebrand factor (vWF) [11] | Angiogenesis and apoptosis [15] | ||
| C4BPB | Complement Component 4 Binding Protein Beta | Inactivation of protein S, which is an important cofactor to activated protein C and constitutes a ligand for the Axl family of receptor tyrosine kinases [16, 17] | Inflammation and apoptosis [16] Proliferation signalling, invasion and apoptosis through Axl receptor tyrosine kinase signalling [18] |
| NME7 | NME/NM23 Family Member 7 | Embryonic Stem Cell Renewal [19] | Metastasis |
| FGB/FGG/FGA | Fibrinogen Beta Chain/ Fibrinogen Gamma Chain/ Fibrinogen Alpha Chain | Formation of fibrin clot | Angiogenesis [11] |
| Immune response [20] | Immune evasion and inflammation | ||
| Augmentation of the proliferative effect of fibroblast growth factor‐2 (FGF‐2) [21] | Proliferative signalling and angiogenesis [21] | ||
| F11 | Coagulation Factor XI | Generation of Factor Xa | Apoptosis [22] |
| Generation of thrombin | Metastasis, angiogenesis, immune evasion and apoptosis [11] | ||
| SLC19A2 | Solute Carrier Family 19 Member 2 | Metabolism | Cancer metabolism |
| F2 | Coagulation Factor II, thrombin | Generation of thrombin | Metastasis, angiogenesis, immune evasion and apoptosis [11] |
| CNTN6 | Contactin 6 | Activating of Notch signalling pathway [23] Mediation of cell surface interactions | Proliferative signalling and metastasis [11] |
| OTUD7A | OTU Deubiquitinase 7A | Modulation of nuclear factor kappa B (NF-κB) expression through interaction with TNF receptor associated factor 6 (TRAF6) | Metastasis [24] |
| SV2C | Synaptic Vesicle Glycoprotein 2C | Modulation of dopamine release [25] | Apoptosis and inflammation [26] |
| SUSD1 | Sushi Domain Containing 1 | Unknown role in carcinogenesis | unknown |
| PROCR | Protein C Receptor | Protein C pathway | Proliferative signalling, invasion, metastasis, apoptosis and immune evasion [27] Angiogenesis [28] |
| ZFPM2 (FOG2) | Zinc Finger Protein, FOG Family Member 2 | GATA transcriptional network | Apoptosis, invasion and inflammation [29] |
| Angiogenesis [30] | |||
| TSPAN15 | Tetraspanin 15 | Mediates signal transduction events that play a role in the regulation of cell activation, growth, development and motility. | Metastasis [31] |
| SLC44A2 | Solute Carrier Family 44 Member 2 | Metabolism | Cancer metabolism |
| FUNDC2 | FUN14 Domain Containing 2 | Modulation of platelet survival [32] | Metastasis, angiogenesis and immune evasion [33] |
| COX7A2L | Cytochrome C Oxidase Subunit 7A2 Like | Regulation of oxidative phosphorylation | Cancer metabolism |
| EPHA3 | EPH Receptor A3 | Regulation of developmental events Regulation of cytoskeletal organization, cell-cell adhesion and cell migration |
Invasion and metastasis [34] Angiogenesis [35] |
| B3GAT2 | Beta-1,3-Glucuronyltransferase 2 | Mismatch repair deficiency [36] | Genome instability and mutation |
| THBD | Thrombomodulin | Protein C pathway Regulation of adhesion molecules [37] |
Angiogenesis [28] Invasion and metastasis [37] |
| LEMD3 (MAN1) | LEM Domain Containing 3 | Regulation of transforming growth factor-beta (TGF-beta) signalling at the inner nuclear membrane | Proliferative signalling, invasion and apoptosis [38] Immune evasion [39] |
| LY86 (MD-1) | Lymphocyte Antigen 86 | Innate Immune System | Inflammation |
| LOC100130298 | HCG1816373-Like | Unknown role in carcinogenesis | Unknown |
The data shown in Table 4 concerning the HUGO nomenclature and the molecular process involved in carcinogenesis were obtained from "Genecards" database (exceptions are referenced).