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  • mProX™ Human SLK Stable Cell Line

    [CAT#: S01YF-1023-PY100]
    Product Category:
    Membrane Protein Stable Cell Lines
    Subcategory:
    Kinase Cell Lines

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    Based on this stable cell line, we also provide cell-based in vitro assays to evaluate the effects of your compounds or antibodies.

    Sub Cat Product Name Target Protein Species Host Cell Type Assay Types Inquiry Datasheet
    S01YF-1222-KX489 Magic™ Human SLK in Vitro Assay Human Kinase Assay

    Product Information

    Target Family
    Kinases/Enzyme
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;NMuMG
    Target Classification
    Kinase Cell Lines
    Target Research Area
    CNS Research
    Related Diseases
    Advanced Sleep Phase Syndrome, Familial, 1; Advanced Sleep Phase Syndrome, Familial, 3
    Gene ID
    Human:2534
    UniProt ID
    Human:P06241

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    The applications of SLK (STE20-like kinase) include its role in promoting ferroptosis of hepatocellular carcinoma (HCC) by stabilizing O-GlcNAc transferase (OGT) and inhibiting O-GlcNAcylation of SLC7A11, its involvement in the development of a mobile app for assessing the quality of life of cancer patients, its association with mortality in vancomycin-resistant enterococcus (VRE) infections, and its use in concurrent septorhinoplasty and endoscopic sinus surgery to improve quality of life.

    Protocols

    Please visit our protocols page.

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    FAQ

    chat Alex Jones (Verified Customer)

    What are the potential applications of SLK inhibitors? May 16 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    Potent and selective inhibitors of SLK, like compound 31, have been identified, which could have therapeutic applications. May 16 2023

    chat Casey Jones (Verified Customer)

    How does SLK contribute to muscle contraction? May 04 2022

    chat Patrick Liam (Creative Biolabs Scientific Support)

    SLK mediates control of actin polymerization, which is crucial for smooth muscle contraction. May 04 2022

    Published Data

    Fig.1 Invasion of NeuNT-expressing cells is hindered by the knockdown of SLK.

    In the chemotaxis assays, NMuMG cells, either expressing NeuNT or the signaling-deficient mutant NYPD, were transfected with SLK siRNA or a non-targeting control. A notable decrease in chemotaxis was detected following SLK depletion.

    Ref: Roovers, K., et al. "The Ste20-like kinase SLK is required for ErbB2-driven breast cancer cell motility." Oncogene 28.31 (2009): 2839-2848.

    Pubmed: 19525980

    DOI: 10.1038/onc.2009.146

    Research Highlights

    Tang, Jianing. et al. "Targeting USP8 Inhibits O-GlcNAcylation of SLC7A11 to Promote Ferroptosis of Hepatocellular Carcinoma via Stabilization of OGT." Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023.
    Hepatocellular carcinoma (HCC) is a highly deadly and aggressive form of cancer in humans. In a recent study, the potential of deubiquitylating enzyme (DUB) inhibitors in treating HCC was investigated. The results showed that targeting ubiquitin specific peptidase 8 (USP8) and using DUB-IN-3 had the most promising anti-cancer effects. Specifically, inhibiting USP8 led to reduced HCC cell proliferation and increased cell ferroptosis. In vivo experiments also showed that USP8 inhibition suppressed tumor growth and lung metastasis. Mechanistic analyses further revealed that USP8 stabilizes O-GlcNAc transferase (OGT) by preventing its K48-specific poly-ubiquitination at the K117 site. Additionally, STE20-like kinase (SLK)-mediated phosphorylation of USP8 at S716 was found to facilitate its interaction with OGT. Notably, it was also discovered that OGT O-GlcNAcylation of solute carrier family 7, member 11 (SLC7A11) at Ser26 is crucial for SLC7A11 to import cystine from the extracellular environment. These findings suggest that targeting USP8 may be a viable option for HCC treatment, as it disrupts the stability of OGT and promotes ferroptosis.
    Tang, Jianing. et al. "Targeting USP8 Inhibits O-GlcNAcylation of SLC7A11 to Promote Ferroptosis of Hepatocellular Carcinoma via Stabilization of OGT." Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2023.
    Pubmed: 37867237   DOI: 10.1002/advs.202302953

    Nakajima Doi, Seiko. et al. "Diabetes and Implantable Cardioverter Defibrillator in Nonischemic Systolic Heart Failure: An Extended Follow-Up Analysis of DANISH." Circulation. Heart failure, 2023.
    This article is about a study that investigated the effect of diabetes and implantable cardioverter defibrillator (ICD) on the outcomes of patients with nonischemic systolic heart failure. The study was an extended follow-up analysis of DANISH, a randomized clinical trial that compared ICD with usual care.
    Nakajima Doi, Seiko. et al. "Diabetes and Implantable Cardioverter Defibrillator in Nonischemic Systolic Heart Failure: An Extended Follow-Up Analysis of DANISH." Circulation. Heart failure, 2023.
    Pubmed: 37753706   DOI: 10.1161/CIRCHEARTFAILURE.123.010606

    Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR CLINICAL PROCEDURES" For licensing inquiries, please contact
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