mProX™ Human HASPIN Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Kinase Cell Lines
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Published Data
Fig.1 HASPIN mRNA levels in breast cancer cell lines.
Given that HASPIN is an intronless gene, the PCR primer set was unable to discriminate between genomic and cDNA. Samples that tested negative for reverse transcriptase (RT) showed no amplification products, indicating that there was no genomic DNA contamination.
Ref: Nishida-Fukuda, Hisayo, et al. "Evaluation of the antiproliferative effects of the HASPIN inhibitor CHR-6494 in breast cancer cell lines." Plos one 16.4 (2021): e0249912.
Pubmed: 33852630
DOI: 10.1371/journal.pone.0249912
Research Highlights
Since threonine 3 of histone 3 is the only substrate for Haspin, inhibiting Haspin may not be as harmful as other anticancer drugs.
Amoussou, Nathalie Gisèle, et al. "Haspin: a promising target for the design of inhibitors as potent anticancer drugs." Drug Discovery Today 23.2 (2018): 409-415.
Pubmed:
29031622
DOI:
10.1016/j.drudis.2017.10.005
The foundation of cancer treatment is the selective elimination of cancerous cells without seriously harming healthy tissues, and new therapeutic targets for the management of tumors are continuously needed in current clinical practice. Most eukaryotes share the atypical protein kinase Haspin, which has been demonstrated to be especially active in cycling cells.
Quadri, Roberto, Sarah Sertic, and Marco Muzi-Falconi. "Roles and regulation of Haspin kinase and its impact on carcinogenesis." Cellular signalling 93 (2022): 110303.
Pubmed:
35278668
DOI:
10.1016/j.cellsig.2022.110303