STRESS AND TOXICITY SIGNALING PATHWAY

The stress and toxicity signaling pathway plays crucial roles in cellular response mechanisms that help cells detect, respond to, and adapt to harmful environmental conditions.

These pathways are integral to understanding how cells cope with oxidative stress, chemical toxins, and other stressors that may lead to cellular damage or disease development. Key molecular players in these pathways include heat shock proteins, kinases, and transcription factors that modulate cellular repair, apoptosis, and detoxification processes.

AnyGenes offers specialized qPCR arrays that provide comprehensive profiling of gene expression within the stress and toxicity signaling pathways. These products are designed to support research by delivering accurate insights into gene expression levels, enabling scientists to explore biomarkers, mechanisms, and responses that are critical for understanding cellular resilience and susceptibility to stress.

Visualization of stress and toxicity signaling pathways with AnyGenes qPCR array, highlighting key mechanisms and biomarkers involved in cellular responses to stress.

In the canonical model of the UPR, unfolded or misfolded proteins activate the three major sensing molecules (IRE1, PERK, and ATF6) at the ER membrane by recruiting the ER chaperone BiP away from the lumenal domains of these proteins. IRE1 is a kinase and ribonuclease that on autophosphorylation activates splicing and produces the active transcription factor XBP1, which induces the expression of ER chaperones, degradation components, and lipid synthesis enzymes. PERK is a kinase that is also activated through dimerization and autophosphorylation and phosphorylates eIF2α to attenuate general protein synthesis. ATF6 is a transcription factor that once released from the ER will move to the Golgi. After processing at this site, it translocates to the nucleus to activate the transcription of chaperone genes. Together, these pathways reduce entry of proteins into the ER, facilitate disposal of the misfolding proteins, and produce the components for the ER to adapt its folding capacity to reach equilibrium. When these pathways fail to reach homeostasis, they can also trigger death. Under severe stress conditions, the synthesis of ATF4 is enhanced in an eIF2α-phosphorylation-independent manner that promotes apoptosis..

KEY SIGNALING PATHWAYS

Unfolded Protein Response (UPR): The UPR is activated in response to endoplasmic reticulum (ER) stress, which can arise from various factors such as protein misfolding or overload.
MAPK Pathways (JNK and p38 MAPK): The c-Jun N-terminal kinase (JNK) and p38 MAPK pathways are pivotal in mediating cellular responses to stressors like UV radiation, heat shock, and inflammatory cytokines.
p53 Pathway: acts as a guardian of the genome by preventing the proliferation of cells with damaged DNA.
Nrf2 Pathway: Nuclear factor erythroid 2-related factor 2 (Nrf2) is a key regulator of the antioxidant response. It activates genes that promote detoxification processes and protect against oxidative stress.

MECHANISMS OF STRESS AND TOXICITY SIGNALING PATHWAY

Detection of Stress Stimuli: The pathway is activated by external stressors like oxidative stress, toxins, or environmental pollutants, initiating a cellular response.
Activation of Key Pathways: Major signaling cascades (e.g., MAPK, NF-kB, JNK) are engaged to regulate cellular stress responses, helping cells adapt or counteract harmful effects.
Defense Mechanisms: These pathways drive essential responses, including antioxidant defenses and DNA repair, aimed at protecting cells from damage.
Apoptosis Initiation: When damage is severe, apoptosis is triggered to remove compromised cells, preventing potential harm to surrounding tissue.
Immune System Coordination: Signaling mechanisms ensure efficient immune clearance of damaged cells, aiding tissue health and resilience.

IMPLICATION IN HEALTH AND DISEASES

Understanding stress and toxicity signaling pathways is crucial for elucidating their roles in various health conditions and diseases:

Chronic Diseases: Dysregulation of stress signaling pathways is implicated in chronic diseases such as diabetes, cardiovascular diseases, and obesity, contributing to inflammation and metabolic dysfunction.
Neurodegenerative Disorders: Oxidative stress is a common factor in neurodegenerative diseases such as Alzheimer's and Parkinson's disease. The accumulation of ROS can lead to neuronal damage, inflammation, and cell death.
Cancer Progression: Many cancers exploit stress signaling pathways to survive under adverse conditions. Tumor cells may activate these pathways to evade apoptosis, enhance proliferation, and promote metastasis.
Autoimmune Diseases: In conditions like lupus and rheumatoid arthritis, stress pathways can exacerbate immune responses, leading to tissue damage and chronic inflammation.
Toxicological Implications: In toxicology, stress response pathways serve as indicators of cellular health and toxicity.

APPLICATIONS IN TOXICOLOGY AND DRUG SCREENING

Understanding stress and toxicity signaling pathways has vital applications in toxicology and drug screening:

Toxicological Assessment: Researchers assess how environmental pollutants and chemicals induce cellular damage, helping to establish safety standards.
Drug Development: By examining how drug candidates interact with stress pathways, researchers can identify compounds that promote beneficial responses while minimizing toxicity.
Biomarker Identification: Specific stress response pathways can serve as biomarkers for early detection of toxicity, enhancing safety evaluations.
Personalized Medicine: Individual variations in stress responses can inform tailored treatments, optimizing therapeutic strategies for better patient outcomes.
Environmental Monitoring: Monitoring the effects of pollutants on signaling pathways helps assess ecosystem health and guide environmental policy.

(1) Welcome MO. Cellular mechanisms and molecular signaling pathways in stress-induced anxiety, depression, and blood-brain barrier inflammation and leakage. Inflammopharmacology. (2020);28(3):643-665.

(2) Liu Y, et al. Signaling pathways of oxidative stress response: the potential therapeutic targets in gastric cancer. Front Immunol. (2023)18:14:1139589.Qu F, et al. Cadmium Exposure: Mechanisms and Pathways of Toxicity and Implications for Human Health. Toxics. (2024)26;12(6):388.

(3) Jennings P. Stress response pathways, toxicity pathways and adverse outcome pathways. Arch Toxicol. (2013);87(1):13-4.

(4) Hotamisligil GH, Davis RJ. Cell Signaling and Stress Responses. Cold Spring Harb Perspect Biol. (2016);8(10):a006072.

(5) Li S, Xia M. Review of High-content Screening Applications in Toxicology. Arch Toxicol. (2019)29;93(12):3387–3396

STRESS & TOXICITY SIGNALING PATHWAY BIOMARKER LIST

Customize your own signaling pathways (SignArrays®) with the factors of your choice!
Simply download and complete our Personalized SignArrays® information file and send it at contact@anygenes.com to get started on your project.

You can check the biomarker list included in this pathway, see below:

Species : Homo sapiens (human)

Signaling Pathways	Product ref	Informations
Stress & Toxicity Signaling Pathway	ST1H1	List infos

Species : Mus musculus (mouse)

Signaling Pathways	Product ref	Informations
Stress & Toxicity Signaling Pathway	ST1M1	List infos

Species : Rattus norvegicus (rat)

Signaling Pathways	Product ref	Informations
Stress & Toxicity Signaling Pathway	*******	List In progress...

Species : Sus Scrofa (Pig)

Signaling Pathways	Product ref	Informations
Stress & Toxicity Signaling Pathway	*******	List In progress...

For more information on prices, please click here