Cloned (Comment) | Organism |
---|---|
gene TTK, quantitative real time reverse transcription PCR enzyme expression analysis | Homo sapiens |
Protein Variants | Comment | Organism |
---|---|---|
additional information | enzyme TTK knockout by siRNA transfection of cell lines PaTu-8988T, Panc1 and S2-028 | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | P33981 | - |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
hTERT-HPNE cell | - |
Homo sapiens | - |
Panc1 cell | - |
Homo sapiens | - |
pancreas | - |
Homo sapiens | - |
pancreatic ductal adenocarcinoma cell | strong overexpression of dual specificity kinase TTK | Homo sapiens | - |
PaTu-8988T cell | - |
Homo sapiens | - |
S2-028 cell | - |
Homo sapiens | - |
Synonyms | Comment | Organism |
---|---|---|
dual specificity kinase | - |
Homo sapiens |
Mps1 | - |
Homo sapiens |
TTK | - |
Homo sapiens |
Organism | Comment | Expression |
---|---|---|
Homo sapiens | TTK kinase is upregulated in pancreatic cancer | up |
General Information | Comment | Organism |
---|---|---|
malfunction | upon TTK knockdown in pancreatic ductal adenocarcinoma cells, cell proliferation is significantly attenuated, whereas apoptosis and necrosis rates are significantly increased. Anchorage-independent growth, a hallmark of malignant transformation and metastatic potential, is strongly impaired in the absence of TTK gene function. Immortalised normal pancreatic hTERT-HPNE cells are not affected by loss of TTK function. Phenotype, overview. The effects in cancer cells are associated with increased formation of micronuclei, suggesting that loss of TTK function in pancreatic cancer cells results in chromosomal instability and mitotic catastrophe | Homo sapiens |
physiological function | enzyme TTK function is critical for growth and proliferation of pancreatic cancer cells | Homo sapiens |