Targeting Signaling Molecules for Developing Anti-Obesity Therapeutics
InquiryOverview of Signaling Molecules in Obesity
Signaling molecules coordinate the body's complex metabolic pathways and physiological processes and are key to metabolic regulation. These molecules act as important messengers, transmitting key information between cells and tissues to maintain energy balance and homeostasis. By decoding and manipulating these biochemical signals, Protheragen precisely intervenes in the signaling molecules to develop innovative therapies to address obesity from the source rather than the symptoms.
Fig.1 Signaling pathways involved in pro-obesity and anti-obesity mechanisms. (Wen, et al., 2022)
Harnessing Signaling Molecules as Targets for Anti-Obesity Therapy
From hormones such as leptin and insulin to neurotransmitters and inflammatory cytokines, the various signaling molecules associated with obesity provide numerous targets for potential anti-obesity therapies. This novel perspective not only broadens our understanding of the underlying mechanisms of obesity but also opens up new avenues for more effective and sustainable treatment options. We help clients develop anti-obesity therapies by targeting signaling molecules through meticulous target identification, target validation, Therapy Development, and Preclinical Research.
Obesity-related Signaling Molecule Targets
- Adipokines
Adipokines are key cell-signaling proteins produced by adipose tissue that regulate energy balance, glucose metabolism, insulin sensitivity, and more. Protheragen uses advanced biotechnology to identify and modulate specific adipokines with potential therapeutic benefits to develop advanced innovative therapies that correct metabolic imbalances caused by obesity and address obesity-related complications. - Tumor Necrosis Factor-alpha (TNF-α)
Protheragen develops effective TNF-α inhibitors or modulators by focusing on the role of TNF-α as a key pro-inflammatory cytokine in obesity and metabolic syndrome. They reduce the inflammatory response, improve insulin sensitivity, and normalize glucose metabolism. Such targeted interventions not only address the symptoms of obesity but also its underlying inflammatory causes, thereby providing a more effective and comprehensive solution. - Transforming Growth Factor (TGF)-β
We address obesity by precisely modulating signaling molecules within the TGF-β pathway to affect adipogenesis and energy metabolism. Our strategy involves developing specific inhibitors and agonists that modulate TGF-β activity. SP-1154, a novel synthetic TGF-β inhibitor, has been reported to reduce high-fat diet-induced obesity and hepatic steatosis in mice.
Methods for Anti-Obesity Therapy Development
In the process of developing obesity treatments targeting these signaling molecule targets, the technologies we use include but are not limited to:
- High-throughput screenings (HTS): Rapidly screen and identify small molecule compounds that interact with target molecules. This technology rapidly screens thousands to millions of compounds to find potential drug candidates.
- Gene Editing: Use powerful editing technologies to knock in, knock out, silence, and overexpress target genes to understand their role in obesity and develop effective Gene Therapies.
- Nanotechnology: Use nanoparticles and nanomaterials to effectively deliver drugs to specific tissues or cells, improve efficacy, and reduce side effects of anti-obesity therapies.
- Bioinformatics: Use algorithms and models to integrate and analyze large data sets from genomics, proteomics, and metabolomics studies to identify new targets and predict the effects of potential therapies.
Evaluating the Efficacy of Anti-obesity Therapies
- Animal Models: We use mammalian obesity models (e.g., Mice, Dogs, Rats) and non-mammalian obesity models (e.g., zebrafish, Drosophila melanogaster) to evaluate the efficacy of anti-obesity therapies. We also study obesity models induced by High-fat Diet, High Sugar, High Protein, or genetic modification.
- Cell Models: We use adipocyte cell lines for in vitro studies to evaluate the effects of anti-obesity therapies on adipocytes at the molecular level.
- Metabolic and biochemical assays: We analyze the effects of therapies on glucose uptake, lipid accumulation, and energy expenditure, as well as changes in hormones such as insulin, leptin, adiponectin, and ghrelin.
Workflow
Applications
- Study how different signaling molecules affect fat storage, energy expenditure, appetite control, and insulin sensitivity to identify new therapeutic targets.
- Study the role of signaling molecules in adipose tissue and other metabolic organs to reveal the molecular basis of obesity and promote the discovery of biomarkers for early detection and prognosis.
- Develop drugs that specifically regulate signaling molecule pathways to provide more effective and personalized treatment options for obesity and its related metabolic disorders.
Advantages
- A team of experts in metabolic research, pharmacology, and biotechnology ensures a high level of scientific and technical support throughout the drug development process.
- We have state-of-the-art laboratory facilities equipped with cutting-edge technologies for high-throughput screening, bioinformatics analysis, and preclinical testing, ensuring efficient and accurate identification of promising signaling molecules.
- Our end-to-end services cover all stages of preclinical research for the development of anti-obesity therapies, such as target screening and identification, lead compound screening and optimization, and animal model studies.
We provide clients with obesity-related analytical services to fully understand the complexity of obesity and provide them with data-driven insights to manage and combat obesity. By leveraging cutting-edge technology and scientific expertise, we provide clients with personalized and effective strategies for obesity research.
Publication Data
DOI: 10.3390/cancers11010024
Journal: Cancers
Published: 2019
IF: 4.5
Results: Obesity contributes to the development of various cancers, including liver and colorectal cancers, at least partially due to chronic, low-grade inflammation induced by obesity. Specifically, the recruitment and activation of immune cell subsets in white adipose tissue lead to an increase in proinflammatory cytokines like TNFα and interleukin-6 (IL-6). These proinflammatory cytokines not only impair insulin action in metabolic tissues but also promote cancer development. Here, the authors summarize the effects of obesity on inflammatory TNFα and IL-6 signaling in hepatocellular carcinoma (HCC) and colorectal cancer (CRC).
Fig.2 The obesity-induced, systemic, low-grade inflammation contributes to the progression of HCC and CRC. (Kern, et al., 2019)
Frequently Asked Questions
What is the timeline of preclinical studies for developing an anti-obesity drug targeting signaling molecules?
The timeline of preclinical studies for anti-obesity drug development targeting signaling molecules depends on many factors, such as the complexity of the target, the type of drug, etc., and usually takes several years. This process includes identifying and validating the target, optimizing the lead compound (including in vivo and in vitro efficacy, specificity, and safety testing, etc.), as well as toxicology studies and pharmacokinetic evaluations.
How can I partner with Protheragen to develop signaling molecule-targeted anti-obesity therapies?
Protheragen provides comprehensive support for the preclinical stage of anti-obesity therapy development using its extensive expertise and cutting-edge drug development platforms. We provide end-to-end services from target screening, lead compound discovery, and optimization, and in vitro activity evaluation to in vivo animal models. Discuss potential collaborations, and tailor-made solutions with us, and leverage our strengths in this field to bring innovative weight loss therapies to market.
Protheragen is at the forefront of developing anti-obesity therapeutics, targeting signaling molecules to provide innovative and scientific approaches to address obesity and its related metabolic disorders. Please feel free to contact us to explore tailored solutions and strategic collaborations to meet specific project needs.
References
- Kern, L.; et al. Obesity-induced TNFα and IL-6 signaling: the missing link between obesity and inflammation-driven liver and colorectal cancers. Cancers. 2019,11(1): 24.
- Wen, X.; et al. Signaling pathways in obesity: mechanisms and therapeutic interventions. Signal transduction and targeted therapy. 2022, 7(1): 298.
All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.