Mitogen-activated protein kinase kinase kinase kinase 4 (MAP4K4) – also known as hepatocyte progenitor kinase-like/germinal center kinase-like kinase (HGK) and Nck-interacting kinase (NIK) – is an enzyme, specifically a serine/threonine (S/T) kinase encoded by the MAP4K4 gene in humans.[5][6]
While MAP4K4 has been found to be upregulated in a wide array of cancers, there is currently limited information regarding its specific involvement. However, there is increasing evidence that suggests MAP4K4 has an important role in the development and progression of cancer, and may serve as a novel target for cancer therapeutics.[6]
Discovery and classification
MAP4K4 is categorized under the mammalian sterile 20 protein (Ste20p) kinase family due to its shared homology with the Ste20p kinase found in budding yeast[5] and is a member of the GCK-IV subfamily. Mammalian MAP4K4 was initially identified in mice as a kinase activator for a protein called Nck[10] followed shortly by identification and cloning of the human orthologue encoded by the MAP4K4 gene.[11]
Structure and expression
In humans, MAP4K4 is encoded by the MAP4K4 gene located on chromosome 2, position q11.2 and consists of 33 exons responsible for its synthesis.[5] It contains approximately 1200 amino acids, has a molecular mass of ~140 KDa.[10][11] and its orthologues across various species share molecular and structural similarities.
Structurally MAP4K4 contains the following domains:[5]
Interdomain - Connects the kinase and CNH domains, facilitates protein-protein interactions. Although it has been identified, its structural components and functionality are currently poorly understood
Figure 1. Schematic representation of MAP4K4 structure, depicts the N-terminal kinase domain, C-terminal citron homology domain (regulatory function) and the interdomain (facilitates protein interactions).[6][12] Note: the numbers indicate amino acid positions.
Alternative splicing of the MAP4K4 gene yields five functional isoforms, all of which display fully homologous kinase and CNH domains but differences in the interdomain domain.[13] While the biological significance of these isoforms remains to be determined, it can be speculated that such variations alter and determine MAP4K4's interactions with other proteins and factors, ultimately leading to the activation/inhibition of different biochemical and physiological cascades.
The mammalian class of Ste20 kinases require phosphorylation at specific sites for full activity. Primary phosphorylation at the activation site in their kinase domain is believed to cause a conformational change in the protein, stabilizing the structure of its activation segment to allow suitable substrate binding.[5] Secondary sites also require phosphorylation for the enzyme to assume full activation and is achieved via autophosphorylation or by upstream kinases.[5]
To date, MAP4K4 has been found to be expressed in all tissue types[11] with a relatively more pronounced expression in the brain and testes.[14] Multiple isoforms of MAP4K4 can be present at any given time in the same cell but the abundance of each isoform in the cell differs depending on the cell-type or tissue-type.[14]
E.g. In humans, the shorter isoform of MAP4K4 is predominantly expressed in organs including the liver, placenta, skeletal muscles while a longer isoform is expressed in the brain
Interactions and signaling
TNF-α
Evidence from mammalian and fly studies indicate that MAP4K4 is involved with tumour necrosis factor alpha (TNF-α) and its c-jun N-terminal kinase (JNK) signaling pathway.[15] MAP4K4 not only mediates TNF-α signaling but also promotes its expression;[11] moreover, TNF-α can elevate MAP4K4 expression using transcription factors[16]
The JNK pathway is implicated in a number of physiological processes and involves JNKs – kinases responsible for the phosphorylation of a downstream protein called c-Jun. This further leads to the increase in expression and activity of specific transcription factors that respond to a variety of cellular stressors, growth factors and cytokines. The activation of the JNK signal transduction pathway by MAP4K4 has been implicated in apoptotic regulation of many different cell types,[17] tumorigenesis and/or inflammation.[7]
p53
p53 is a tumour suppressor gene and is involved with cellular response to stress. When expressed, the cell cycle is halted in the G1 phase and can induce senescence or apoptosis. Mutations to the p53 gene are often found in many types of cancers.
The MAP4K4 gene contains four binding sites for p53. Upon binding, p53 up-regulates MAP4K4 expression leading to the activation of the JNK signaling pathway. siRNA knockdown experiments have also shown a reduction of p53 induced apoptosis.[17] Current evidence therefore suggests that MAP4K4 has a modulating effect on p53 induced apoptosis in the JNK signaling pathway.
Clinical significance
Glucose uptake and insulin function
MAP4K4 has been identified to be involved in the negative regulation of insulin-dependent glucose transport. There is increasing evidence suggesting cytokines such as TNF-α mediate biological effects antagonistic to insulin action and induce inflammation observed in obesity.[18][19] TNF-α specifically attenuates the signaling pathway initiated by insulin receptors, reducing the amount of glucose transport and uptake;[20] and it is believed that MAP4K4 functions as an upstream signaling element in the TNF-α signaling cascade.[11]
A recent siRNA screen identified the involvement of MAP4K4 in the regulation of the glucose transporter GLUT4.[21] The silencing of MAP4K4 in adipocytes elevated the expression of peroxisome proliferator-activated receptor y (PPARy) – a nuclear hormone receptor responsible for the regulation of genes associated with adipocyte differentiation, including GLUT4.[22] siRNA silencing of MAP4K4 appears to prevent insulin resistance, restoring insulin sensitivity in human skeletal muscles by down-regulating the TNF-α signaling cascade[23] and inhibits the TNF-α-induced depletion of PPARy and GLUT4.[21] Additionally, miRNA silencing of MAP4K4 in pancreatic beta-cells conferred protection against TNF-α repression of insulin transcription and secretion,[24] further confirming that MAP4K4 targeting is a potential strategy for diabetes prevention and treatment.[24]
Atherosclerosis
Atherosclerosis is the result of an inflammatory response to lipid-mediated vascular damage. It has been identified that cytokines such as TNF-α induce the expression of pro-inflammatory genes to synthesize leukocyte adhesion molecules and chemokines.[25] Endothelial cells highly express MAP4K4[9] and recent studies have reported that MAP4K4 enhances endothelial permeability.[26] This consequently contributes to the development of atherosclerosis due to the promotion of leukocyte extravasation, transport of oxidized lipids and the formation of plaques.[9]
Silencing of endothelial MAP4K4 ameliorated the development of atherosclerosis in mice.[27] Additionally, treatment of a MAP4K4 protein kinase inhibitor in mice significantly reduced plaque progression and promoted plaque regression[27] suggesting therapeutic targeting of MAP4K4 may be a beneficial strategy for cardiovascular disease.
Cancer
The biggest causes of death for patients with cancer are tumour invasion and metastasis – processes that are highly correlated with cell migration and motility.[28] There is limited information regarding how MAP4K4 is involved in cancer but studies have shown that MAP4K4 is overexpressed in a number of cancer types including lung, prostate, pancreatic and ovarian cancer where such up-regulation is associated with increased cell migration, adhesion and invasiveness.[7]
Several studies have identified MAP4K4 as an upstream regulator of proteins associated with cytoskeletal dynamics or adhesion. Deletion of the MAP4K4 gene appears to affect membrane dynamics in endothelial cells, resulting in reduced cell migration and impaired angiogenesis;[29] while an overexpression significantly elevates the rate of cell invasion and morphogenesis.[14]
^ abcBuburuzan L, Luca C (2011). "MAP4K4 a possible new biomarker in cancer therapy". Analele Stiintifice Ale Universitatii" al. I. Cuza" Din Iasi.(Serie Noua). Sectiunea 2. A. Genetica Si Biologie Moleculara. 12 (2).
^Liang JJ, Wang H, Rashid A, Tan TH, Hwang RF, Hamilton SR, Abbruzzese JL, Evans DB, Wang H (November 2008). "Expression of MAP4K4 is associated with worse prognosis in patients with stage II pancreatic ductal adenocarcinoma". Clinical Cancer Research. 14 (21): 7043–9. doi:10.1158/1078-0432.ccr-08-0381. PMID18981001. S2CID8224034.
^Hao JM, Chen JZ, Sui HM, Si-Ma XQ, Li GQ, Liu C, Li JL, Ding YQ, Li JM (March 2010). "A five-gene signature as a potential predictor of metastasis and survival in colorectal cancer". The Journal of Pathology. 220 (4): 475–89. doi:10.1002/path.2668. hdl:10026.1/10314. PMID20077526. S2CID45964500.
Chaudhary PM, Eby MT, Jasmin A, Kumar A, Liu L, Hood L (September 2000). "Activation of the NF-kappaB pathway by caspase 8 and its homologs". Oncogene. 19 (39): 4451–60. doi:10.1038/sj.onc.1203812. PMID11002417. S2CID8314797.
Overview of all the structural information available in the PDB for UniProt: O95819 (Mitogen-activated protein kinase kinase kinase kinase 4) at the PDBe-KB.
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