Cancer Protein Description

This report provides a detailed description of a selected cancer protein with information collected from various sources, including UniProt, the Wellcome Trust Sanger Institute’s Catalogue of Somatic Mutations in Cancer (COSMIC), and the Atlas of Genetics and Cytogenetics in Oncology and Haematology.


Protein Name: MAPK14
Gene Name: MAPK14
Protein Full Name: Mitogen-activated protein kinase 14
Alias: CRK1; CSAID binding protein; CSBP; CSBP1; CSBP2; CSPB1; Cytokine suppressive anti-inflammatory drug binding protein; EC 2.7.11.24; Kinase p38-alpha; MAP kinase MXI2; MAP kinase p38; MAPK14; MAX-interacting protein 2; Mitogen-activated protein kinase p38; MK14; MXI2; P38; P38 MAP kinase; P38 MAPK-alpha; PRKM14; PRKM15
Mass (Da): 41293
Number AA: 360
UniProt ID: Q16539
Locus ID: 1432
COSMIC ID: MAPK14
Gene location on chromosome: 6p21.31
Cancer protein type: OP/TSP
Effect of cancer mutation on protein: UNCLEAR
Effect of active protein on cancer: MIXED
Number of cancer specimens: 20513
Percent of cancer specimens with mutations: 0.33
Normal role description: MAPK14 is a protein-serine/threonine kinase that is activated by pro-inflammatory cytokines, environmental stress and LPS, via phosphorylation by MAP kinase kinases, or autophosphorylation. Its substrates include the transcription regulators ATF2, MEF2C, and MAX; the cell cycle regulator CDC25B; and p53, which indicates that MAPK14 plays a role in stress-related transcription and in cell cycle regulation, as well as in the genotoxic stress response. It is a key player in the maintenance of hematopoiesis homeostasis, as it balances both proliferative and growth inhibitory signals from growth factors/cytokines that regulate hematopoiesis. Alterations in this controlled balance could result in either overproduction or depletion of myelosuppressive cytokines, which could lead to the development of various types of bone marrow failures.
Commentary on involvement of protein in cancer: 1/74 gastric-, 1/477 CNS-, 1/359 lung-, and 2/86 ovarian cancer samples were also mutated (Sanger COSMIC)


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