mProX™ Human TNK2 Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 TNK2 knockdown suppresses tumor formation.
The different tumors' expression of TNK2 or beta actin, which was found by western blotting with certain antibodies in HCC1395 xenografted tumors, is displayed.
Ref: Wu, Xinyan, et al. "The non-receptor tyrosine kinase TNK2/ACK1 is a novel therapeutic target in triple negative breast cancer." Oncotarget 8.2 (2017): 2971.
Pubmed: 27902967
DOI: 10.18632/oncotarget.13579
Research Highlights
Cancer progresses because dysregulated tyrosine kinase signaling modifies cellular homeostasis. The identification of ACK1, sometimes referred to as activated Cdc42-associated kinase 1 or TNK2, as an oncogenic kinase and a non-receptor tyrosine kinase (non-RTK), has revealed new pathways by which tyrosine kinase signaling advances the development of cancer.
Mahajan, Kiran, and Nupam P. Mahajan. "ACK1/TNK2 tyrosine kinase: molecular signaling and evolving role in cancers." Oncogene 34.32 (2015): 4162-4167.
Pubmed:
25347744
DOI:
10.1038/onc.2014.350
The disorders involving these 122 target proteins were subjected to enrichment analysis, and the findings showed that CRC had the strongest connection. Additionally, the development of colorectal cancer (CRC) was linked with 47 distinct target proteins. This adds to the evidence that the tiny chemical molecule has CRC-inhibiting properties. TNK2 was thus thought to be a viable therapeutic target for the management of metastatic colorectal cancer.
Qi, Lu, and Yanqing Ding. "TNK2 as a key drug target for the treatment of metastatic colorectal cancer." International journal of biological macromolecules 119 (2018): 48-52.
Pubmed:
30036625
DOI:
10.1016/j.ijbiomac.2018.07.124