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  • mProX™ Human SPHK2 Stable Cell Line

    [CAT#: S01YF-1023-PY102]
    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-KX491 Magic™ Human SPHK2 in Vitro Assay Human Kinase Assay

    Product Information

    Target Family
    Kinases/Enzyme
    Target Protein Species
    Human
    Host Cell Type
    HEK293;CHO-K1;Huh-7
    Target Classification
    Kinase Cell Lines
    Target Research Area
    Immunology Research
    Related Diseases
    Ureteral Obstruction; Dermatitis, Atopic, 7
    Gene ID
    Human:56848
    UniProt ID
    Human:Q9NRA0

    Product Properties

    Biosafety Level
    Level 1
    Activity
    Yes
    Quantity
    10⁶ cells per vial
    Applications
    SPHK2 (sphingosine kinase 2) has various applications in different fields. In the context of alcoholic liver disease (ALD), targeting SPHK2 with red rice seed coat extract (RRA) was found to improve gut microbiota composition, restore intestinal barrier, and decrease lipopolysaccharide (LPS) levels, thereby ameliorating ALD. In pulmonary hypertension (PH), the SPHK2/S1P axis was found to promote smooth muscle cell histone acetylation, leading to vascular remodeling. In prostate cancer, inhibiting SPHK1/2 with SKI-178 was shown to inhibit cancer cell growth and migration. Additionally, novel SPHK2 inhibitors were designed and synthesized for potential antitumor activity. Lastly, miR-137 was found to be downregulated in glioma and targeting SPHK2 with miR-137 promoted M1-type tumor-associated macrophage polarization, suggesting its potential as a diagnostic biomarker and therapeutic strategy for glioma treatment.

    Protocols

    Please visit our protocols page.

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    FAQ

    chat Jordan Jones (Verified Customer)

    How does SPHK2 contribute to gastric cancer progression? Feb 19 2023

    chat Patrick Liam (Creative Biolabs Scientific Support)

    METTL3-mediated m6A methylation of SPHK2 promotes gastric cancer progression by targeting KLF2. Feb 19 2023

    chat Skyler Johnson (Verified Customer)

    What is the impact of miR-153-3p on SPHK2 in gastric cancer? Oct 04 2021

    chat Patrick Liam (Creative Biolabs Scientific Support)

    miR-153-3p attenuates the development of gastric cancer by suppressing SPHK2. Oct 04 2021

    Published Data

    Fig.1 Hepatic insulin signaling is compromised by the downregulation of SphK2.

    In the Huh7 hepatic cell line, a knockdown of SphK2 was achieved through the application of lentiviral-based shRNA, followed by treatment with insulin at specified concentrations for a duration of 15 minutes. Subsequent Western blot analyses were carried out.

    Ref: Aji, Gulibositan, et al. "Regulation of hepatic insulin signaling and glucose homeostasis by sphingosine kinase 2." Proceedings of the National Academy of Sciences 117.39 (2020): 24434-24442.

    Pubmed: 32917816

    DOI: 10.1073/pnas.2007856117

    Research Highlights

    Chen, Yuxu. et al. "Red Rice Seed Coat Targeting SPHK2 Ameliorated Alcoholic Liver Disease via Restored Intestinal Barrier and Improved Gut Microbiota in Mice." Nutrients, 2023.
    Alcoholic liver disease (ALD) is a prevalent chronic liver disease and a growing global health concern that necessitates the development of new treatments. This study aimed to evaluate the therapeutic potential of red rice extract (Monascus purpureus) in alleviating alcoholic liver injury in a mouse model. The results demonstrate the efficacy of RRME in mitigating the effects of ALD. This research highlights the potential of RRME as a novel therapeutic agent for the management of ALD.
    Chen, Yuxu. et al. "Red Rice Seed Coat Targeting SPHK2 Ameliorated Alcoholic Liver Disease via Restored Intestinal Barrier and Improved Gut Microbiota in Mice." Nutrients, 2023.
    Pubmed: 37836459   DOI: 10.3390/nu15194176

    Dushani C U Ranasinghe, A. et al. "Altered Smooth Muscle Cell Histone Acetylome by the SPHK2/S1P Axis Promotes Pulmonary Hypertension." Circulation research, 2023.
    The study delved into the enigmatic epigenetic regulation of vascular remodeling in pulmonary hypertension (PH), aiming to uncover upstream factors disrupting this equilibrium. Employing various methodologies, including RNA-seq databases and biochemical assays, it revealed that histone acetylation significantly influences transcription machinery in human pulmonary artery smooth muscle cells, particularly in PH-afflicted cells. The research also spotlighted the heightened presence of SPHK2 in iPAH lung tissue, demonstrating its pivotal role in catalyzing histone H3K9 acetylation through EMAP II. Inhibiting SPHK2 mitigated hypoxia-induced PH in mice. Furthermore, the study identified pulmonary vascular endothelial cells as key players in this epigenetic modulation process. Ultimately, these findings offer potential therapeutic avenues for mitigating PH vascular remodeling by targeting SPHK2 and histone acetylation.
    Dushani C U Ranasinghe, A. et al. "Altered Smooth Muscle Cell Histone Acetylome by the SPHK2/S1P Axis Promotes Pulmonary Hypertension." Circulation research, 2023.
    Pubmed: 37698017   DOI: 10.1161/CIRCRESAHA.123.322740

    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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