Hydrogen Gas / HO-1 Cancer Research Results

H2, Hydrogen Gas: Click to Expand ⟱
Features:
Hydrogen Gas, Powerful Antioxidant
Mechanistically, H₂ is most defensibly framed as a selective antioxidant + anti-inflammatory signaling modulator (often via Nrf2↑ and NF-κB↓ / NLRP3↓), with strongest clinical relevance in oncology being reduction of treatment toxicities (radiation/CCRT side-effects), with mixed/early evidence for direct anticancer effects.

1.Antioxidant and Nrf2/ARE Pathway: activate Nrf2, which induces antioxidant enzymes.
2.NF-κB Pathway: reported to inhibit NF-κB activation, thereby reducing inflammatory cytokine production
3.Mitochondrial Apoptosis Pathway
4.MAPK (Mitogen-Activated Protein Kinases) Pathway
5.PI3K/Akt/mTOR Pathway
6.Inflammatory Cytokine Signaling: Reducing cytokines (such as IL-6, TNF-α)
7.p53 Pathway
8.Autophagy Pathways: might regulate autophagy, (dual roles in cancer)

Example unit sometimes used in studies
Example Canadian Supplier

Hydrogen gas can be generated in small amount by hydrogenase of certain members of the human gastrointestinal tract microbiota from unabsorbed carbohydrates in the intestine through degradation and metabolism, which then is partially diffused into blood flow and released and detected in exhaled breath, indicating its potential to serve as a biomarker.

Many studies have shown that H2 therapy can reduce oxidative stress. This, however, contradicts radiation therapy and chemotherapy, in which ROS are required to induce apoptosis and combat cancer. Yet many studies show chemoprotective and radioprotective and some even show chemosentizing
Nevertheless there are some papers claiming ROS ↑ for cancer cells

Hydrogen Gas in Water is also used.
- the amount of H2 dissolved in solutions is limited: up to 0.8 mM (1.6 mg/L) H2 can be dissolved in water under atmospheric pressure at room temperature


Hydrogen Gas — molecular hydrogen (H₂) is a small, neutral diatomic gas investigated as a therapeutic medical gas and redox-signaling modulator. It rapidly diffuses across biological membranes and can be administered by inhalation or indirectly as hydrogen-rich water (HRW), hydrogen-rich saline, or hydrogen-releasing materials. H₂ is best classified as an experimental therapeutic gas rather than a conventional antioxidant drug. Standard abbreviations are H₂ for molecular hydrogen and HRW for hydrogen-rich water. Endogenous H₂ is also produced by intestinal microbial fermentation. Its biological effects appear to involve modulation of oxidative stress, inflammation, mitochondrial function, cell-death signaling, and immune metabolism rather than indiscriminate ROS scavenging alone.

Primary mechanisms (ranked):

  1. Redox modulation and selective suppression of highly damaging oxidative/nitrosative stress, with secondary NRF2-dependent antioxidant adaptation.
  2. Suppression of inflammatory signaling, particularly NF-κB and associated cytokine pathways.
  3. Mitochondrial and metabolic modulation, including preservation or remodeling of mitochondrial bioenergetics and PGC-1α-linked signaling.
  4. Immune modulation, including reported restoration of metabolically exhausted CD8+ T-cell function in cancer.
  5. Context-dependent regulation of tumor-cell ROS, apoptosis, pyroptosis, differentiation, proliferation, and PI3K/Akt/mTOR signaling.
  6. Protection of normal tissues from chemotherapy- and radiotherapy-associated oxidative and inflammatory injury.

Bioavailability / PK relevance: H₂ has unusually rapid tissue diffusion because of its very small, nonpolar structure, but tissue exposure is transient because hydrogen is rapidly redistributed and exhaled. Inhalation provides continuing systemic exposure during administration, whereas HRW delivers a comparatively small finite H₂ dose that falls rapidly after preparation and ingestion. At approximately atmospheric pressure and room temperature, water saturation is only about 1.6 mg/L H₂, approximately 0.8 mmol/L. Biological efficacy therefore depends strongly on route, concentration, treatment duration, and proximity of H₂ generation to the target tissue.

In-vitro vs systemic exposure relevance: H₂ does not behave like a conventional concentration-maintained small-molecule drug. Gas-equilibrated cell culture can provide sustained H₂ exposure that is difficult to reproduce with a single oral dose of HRW. Conversely, inhalation can continuously replenish dissolved H₂ during treatment. Results from prolonged gas-equilibrated cultures, high-pressure systems, or locally generated H₂ nanomaterials should therefore not automatically be extrapolated to ordinary hydrogen-water exposure.

Clinical evidence status: Small human studies and randomized adjunctive trials exist, but H₂ is not an established anticancer therapy. The most credible oncology application currently is supportive treatment during chemotherapy or radiotherapy. A 2025 randomized study in cervical-cancer patients receiving concurrent chemoradiotherapy reported reduced acute radiation enteritis and inflammatory responses with adjunctive H₂/O₂ inhalation without an apparent reduction in tumor-control efficacy. Direct antitumor evidence remains predominantly preclinical, observational, or derived from small uncontrolled cancer cohorts. Trials of HRW during glioma radiochemotherapy and other indications remain exploratory. H₂ should therefore be classified as experimental adjunct/supportive therapy rather than standalone cancer treatment.

Hydrogen Gas Cancer-Relevant Mechanisms

Rank Pathway / Axis Cancer Cells Normal Cells TSF Primary Effect Notes / Interpretation
1 Redox and reactive oxygen species regulation ROS ↑ or ↓ (model-dependent) Excess ROS ↓; oxidative damage ↓ P, R Redox modulation H₂ should not be treated as a simple universal ROS scavenger. Normal-tissue studies predominantly show reduced oxidative injury, whereas some tumor models paradoxically show ROS ↑ and ROS-dependent tumor cell death.
2 NRF2 antioxidant stress response NRF2 ↔ or ↑ (context-dependent) NRF2 ↑; HO-1 ↑; SOD ↑; GSH-associated defenses ↑ R, G Adaptive antioxidant signaling NRF2 activation is mechanistically important mainly for cytoprotection and stress adaptation rather than as a consistent direct anticancer mechanism.
3 NF-κB inflammatory signaling NF-κB ↓ (context-dependent) NF-κB ↓; inflammatory injury ↓ R, G Anti-inflammatory signaling Frequently accompanied by IL-6 ↓, TNF-α ↓ and IL-1β ↓. This pathway is particularly relevant to normal-tissue protection during inflammatory injury and cancer therapy.
4 Mitochondrial bioenergetics and PGC-1α Mitochondrial function ↑ in exhausted immune cells; tumor response model-dependent Mitochondrial damage ↓; ATP homeostasis ↑ R, G Bioenergetic remodeling H₂ can improve mitochondrial resilience. In cancer, an important proposed mechanism is metabolic restoration of exhausted antitumor lymphocytes rather than direct mitochondrial poisoning of tumor cells.
5 CD8 T-cell exhaustion and antitumor immunity Indirect tumor suppression ↑ CD8+ T-cell metabolic fitness ↑ G Immune restoration Clinical observations in colorectal and lung cancer suggest restoration of exhausted CD8+ T-cell function, including mitochondrial and CoQ10-associated effects. Evidence remains preliminary.
6 PI3K Akt mTOR proliferative signaling PI3K ↓; p-Akt ↓; mTOR signaling ↓ (model-dependent) ↔ or context-dependent G Growth suppression Reported particularly in experimental colorectal-cancer models. This is not yet established as a reproducible systemic mechanism in patients.
7 NLRP3 caspase-1 GSDMD pyroptosis ROS ↑; NLRP3 ↑; caspase-1 ↑; GSDMD-mediated pyroptosis ↑ (model-dependent) NLRP3 commonly ↓ during inflammatory injury R, G Context-dependent inflammatory cell death An important example of opposite modulation by biological context. H₂ induced ROS-dependent NLRP3-mediated pyroptosis in an endometrial-cancer model, whereas normal-tissue inflammatory models commonly show NLRP3 suppression.
8 Tumor proliferation and differentiation Proliferation ↓; differentiation ↑ (model-dependent) Generally ↔ G Tumor phenotype modulation Glioblastoma models report differentiation of glioma stem-like cells and reduced tumor growth. Generalization to other cancers is uncertain.
9 Angiogenesis and hypoxic signaling HIF-1α ↓; VEGF ↓ (model-dependent) VEGF responses mixed G Angiogenic suppression Preclinical evidence suggests inhibition in selected tumor models but does not establish a general antiangiogenic clinical effect.
10 Glycolytic metabolism HK2 ↓; PFK ↓; glycolysis ↓; lactate production ↓ (model-dependent) ↔ or context-dependent G Metabolic growth restriction Reported in selected experimental cancer systems and should remain secondary until replicated across models.
11 Chemosensitization Therapeutic response ↑ in selected models Chemotherapy-associated organ injury ↓ G Adjunctive treatment modulation H₂ has produced both chemoprotective normal-tissue effects and occasional tumor chemosensitization. Protection of normal tissues should not be interpreted as established protection of tumors.
12 Radiotherapy tissue protection Tumor control apparently ↔ in limited human data Radiation-associated oxidative and inflammatory injury ↓ R, G Supportive radioprotection A randomized cervical-cancer study reported reduced acute radiation enteritis during chemoradiotherapy without evidence of compromised short-term antitumor efficacy. Larger confirmation is required.
13 Clinical Translation Constraint Direct anticancer efficacy unproven Generally well tolerated in studied protocols G Exposure and evidence limitation H₂ exposure varies substantially with inhaled concentration, flow, duration, HRW concentration, storage, and delivery technology. Gas mixtures containing high H₂ concentrations require engineered control because hydrogen is flammable and explosive in air. No standardized oncology dose or approved anticancer indication exists.

P: 0–30 min     R: 30 min–3 hr     G: >3 hr



Hydrogen Gas and Alzheimer’s disease: Molecular hydrogen has substantial preclinical neuroprotective evidence and limited early human evidence in Alzheimer’s disease and mild cognitive impairment. Proposed mechanisms include oxidative-stress suppression, neuroinflammation reduction, mitochondrial protection, BDNF-related signaling, and reductions in Aβ/BACE-associated pathology and tau phosphorylation. H₂ readily diffuses into the CNS, making delivery biologically plausible, but clinical evidence remains insufficient to classify it as a disease-modifying AD treatment.

Clinical evidence status: Preclinical evidence is extensive relative to the small clinical literature. Human studies include an open-label inhalation pilot in AD, a single-arm biomarker study, and a randomized hydrogen-rich-water study in mild cognitive impairment. Reported cognitive or biomarker improvements are hypothesis-generating; adequately powered randomized trials with validated AD endpoints are still needed.

Hydrogen Gas Alzheimer-Relevant Mechanisms

Rank Pathway / Axis Modulation TSF Primary Effect Notes / Interpretation
1 Oxidative and mitochondrial stress ROS ↓; lipid oxidation ↓; mitochondrial damage ↓ P, R Neuroprotection One of the most consistently reproduced effects in experimental neurodegeneration models.
2 Neuroinflammatory signaling NF-κB ↓; IL-1β ↓; IL-6 ↓; TNF-α ↓ R, G Neuroinflammation suppression Likely interconnected with redox and glial responses.
3 NRF2 antioxidant response NRF2 ↑; HO-1 ↑; endogenous antioxidant defenses ↑ R, G Cellular stress resistance Secondary adaptive mechanism rather than simple chemical radical scavenging.
4 Amyloid beta and BACE signaling Aβ ↓; BACE-associated processing ↓ (model-dependent) G Amyloid pathology reduction Demonstrated mainly in experimental models; human disease-modifying evidence is not established.
5 Tau phosphorylation p-tau ↓ (model-dependent) G Tau pathology attenuation Supported primarily by animal and experimental hydrogen-delivery studies.
6 BDNF and neuronal plasticity BDNF ↑; neuronal plasticity ↑ G Cognitive and synaptic support Reported across several neurologic injury models and investigated as a biomarker in human inhalation studies.
7 NLRP3 inflammasome NLRP3 ↓ R, G Microglial inflammatory suppression Potential connection between oxidative stress, innate immune activation, and neurodegeneration.
8 Cognition and memory Memory ↑; cognitive performance ↑ (model-dependent) G Functional outcome Robust in several animal paradigms but human trials remain small and heterogeneous.
9 Clinical Translation Constraint Evidence insufficient for established AD treatment G Clinical evidence limitation Existing human studies are small, often uncontrolled, or use surrogate endpoints. Optimal concentration, inhalation duration, treatment schedule, and long-term efficacy remain unresolved.

P: 0–30 min     R: 30 min–3 hr     G: >3 hr
HO-1, HMOX1: Click to Expand ⟱
Source:
Type:
(Also known as Hsp32 and HMOX1)
HO-1 is the common abbreviation for the protein (heme oxygenase‑1) produced by the HMOX1 gene.
HO-1 is an enzyme that plays a crucial role in various cellular processes, including the breakdown of heme, a toxic molecule. Research has shown that HO-1 is involved in the development and progression of cancer.
-widely regarded as having antioxidant and cytoprotective effects
-The overall activity of HO‑1 helps to reduce the pro‐oxidant load (by degrading free heme, a pro‑oxidant) and to generate molecules (like bilirubin) that can protect cells from oxidative damage

Studies have found that HO-1 is overexpressed in various types of cancer, including lung, breast, colon, and prostate cancer. The overexpression of HO-1 in cancer cells can contribute to their survival and proliferation by:
  Reducing oxidative stress and inflammation
  Promoting angiogenesis (the formation of new blood vessels)
  Inhibiting apoptosis (programmed cell death)
  Enhancing cell migration and invasion
When HO-1 is at a normal level, it mainly exerts an antioxidant effect, and when it is excessively elevated, it causes an accumulation of iron ions.

A proper cellular level of HMOX1 plays an antioxidative function to protect cells from ROS toxicity. However, its overexpression has pro-oxidant effects to induce ferroptosis of cells, which is dependent on intracellular iron accumulation and increased ROS content upon excessive activation of HMOX1.

-Curcumin   Activates the Nrf2 pathway leading to HO‑1 induction; known for its anti‑inflammatory and antioxidant effects.
-Resveratrol  Induces HO‑1 via activation of SIRT1/Nrf2 signaling; exhibits antioxidant and cardioprotective properties.
-Quercetin   Activates Nrf2 and related antioxidant pathways; contributes to anti‑oxidative and anti‑inflammatory responses.
-EGCG     Promotes HO‑1 expression through activation of the Nrf2/ARE pathway; also exhibits anti‑inflammatory and anticancer properties.
-Sulforaphane One of the most potent natural HO‑1 inducers; triggers Nrf2 nuclear translocation and upregulates a battery of phase II detoxifying enzymes.
-Luteolin    Induces HO‑1 via Nrf2 activation; may also exert anti‑inflammatory and neuroprotective effects in various cell models.
-Apigenin   Has been reported to induce HO‑1 expression partly via the MAPK and Nrf2 pathways; also known for anti‑inflammatory and anticancer activities.
Scientific Papers found: Click to Expand⟱
7482- H2,    Molecular Hydrogen Therapy: Mechanisms, Delivery Methods, Preventive, and Therapeutic Application
- Review, Var, NA - Review, IBD, NA - Review, Stroke, NA - Review, Sepsis, NA - Review, AD, NA
Dose↝, *Inflam↓, *IL1β↓, *IL6↓, *TNF-α↓, *neuroP↑, *mTOR↓, *IL10↑, *TGF-β↑, *Sepsis↓, *NRF2↑, *antiOx↑, *Catalase↑, *SOD↑, *GPx↑, *ROS↓, *HO-1↑, *PI3K↑, *Akt↑, *hepatoP↑, *MPO↓, *cardioP↑, CDK4↓, CDK6↑, CD47↓, PI3K↓, Akt↓, Hif1a↓, selectivity↑, *MMP↑, *ATP↑, *ER Stress↓, *CHOP/DDIT3↓, *Casp12↓, *GRP78/BiP↓, *p38↓, *p‑JNK↓, *LC3‑Ⅱ/LC3‑Ⅰ↑, *p‑eIF2α↓, *ATF4↓, *XBP-1↓, *Imm↑, *IFN-γ↓, *IL4↓, *GranB/GZMB↓, NK cell↑, radioP↑, *CD4+↑, CD8+↑, *Dose↝, *other↑, *Dose↝, *antiPs↑, *BioAv↝, *GutMicro↑, Dose↝, *IBI↑, TumCP↓, TumCI↓, TumCMig↓, CD8+↑, PGC-1α↑, Akt↓, SCD1↓, *MDA↓, eff↑, *APP↓, *BACE/β-secretase↓, *Aβ↓, *cognitive↑, *neuroP↑, NP/CIPN↓, *Stroke↓, *NLRP3↓, *ALAT↓, *AST↓, *LPS↓, *hepatoP↑, chemoP↑, *creat↓, *Urea↓, *RenoP↑, *eff↑, Apoptosis↑, XIAP↓, IAP2/BIRC3↓, TumVol↓, MALAT1↓, EZH2↓, miR-124-3p↓, eff↑, ChemoSen↑, *compII↑, *compIII↑, *LDL↓, *Obesity↓, QoL↑, PFS↑,
3787- H2,    Hydrogen, a Novel Therapeutic Molecule, Regulates Oxidative Stress, Inflammation, and Apoptosis
- Review, AD, NA
*Inflam↓, *antiOx↑, *ROS↓, *other↝, *NF-kB↓, *IL2↓, *IL6↓, *TNF-α↓, *HO-1↑, Apoptosis↑, TumAuto↑, *Sepsis↓, *NLRP3↓, Pyro↑,
7489- H2,    Molecular Hydrogen in the Treatment of Respiratory Diseases
- Review, Asthma, NA
*antiOx↑, *Inflam↓, *Apoptosis↓, *Dose↓, *Dose↝, *eff↑, *ROS↓, *RNS↓, *NRF2↑, *HO-1↑, *Fenton↓, *NLRP3↓, *NADPH↓, *NOX4↓, *NOX↓, *MPO↓, *NF-kB↓, *TNF-α↓, *IL6↓, *IL1β↓, *HMGB1↓, *IL4↑, *IL10↑, *M2 MC↑, *Treg lymp↝, *Bcl-2↑, *Bcl-xL↑, *PI3K↑, *Akt↑, *JAK2↑, *STAT3↑, *Dose↑, *CD4+↑, *CD25+↑, *FOXP3↑, *MDA↓, *SOD↑, *Catalase↑, *Casp3↓, *Casp9↓, *TBARS↓, *SpO2↑, *VitE↓, *OS↑, *Weight↑, *DNAdam↓, *PGE2↓, *MCP1/CCL2↓, *lipid-P↓, *TumCP↓, *tumCV↓, *TumCMig↓, *TumCI↓, TumW↓, TumVol↓, selectivity↑, QoL↑, ChemoSen↑, chemoP↑, radioP↑, ROS↑, NLRP3↑, Casp3↑, VEGF↓, Wnt↓, β-catenin/ZEB1↓,
3773- H2,    Role and mechanism of molecular hydrogen in the treatment of Parkinson’s diseases
- Review, Park, NA
*neuroP↑, *antiOx↑, *Inflam↓, *ROS↓, *NADPH↓, *NRF2↑, *BBB↑, *IL1β↓, *IL6↓, *TNF-α↓, *NF-kB↓, *NLRP3↓, *Sepsis↓, *p‑mTOR↓, *AMPK↑, *SIRT1↑, *HO-1↑,
2521- H2,    Oxyhydrogen Gas: A Promising Therapeutic Approach for Lung, Breast and Colorectal Cancer
- Review, CRC, NA - Review, Lung, NA - Review, BC, NA
Inflam↑, ROS↓, ChemoSen↑, p‑PI3K↓, p‑Akt↓, QoL↑, GutMicro↑, chemoP↑, radioP↑, *NRF2↑, *Catalase↑, *GPx↑, *HO-1↑, *SOD↑, *TNF-α↓, *IL4↓, *IL6↓, ChemoSen↑, Appetite↑, cognitive↑, Pain↓, Sleep↑, other?,
2516- H2,    Hydrogen Gas in Cancer Treatment
- Review, Var, NA
*Half-Life↓, *ROS↓, *selectivity↑, *SOD↑, *HO-1↑, *NRF2↑, *chemoP↑, *radioP↑, ROS↑, *Inflam↓, eff↑, *TNF-α↓, *IL6↓, *cl‑Casp8↑, *Bax:Bcl2↓, *Apoptosis↓, *cardioP↑, *hepatoP↑, *RenoP↑, *chemoP↑, eff↝, chemoP↑, radioP↑, eff↑, TumCG↓, Ki-67↓, VEGF↓, selectivity↑,
2514- H2,    Hydrogen: A Novel Option in Human Disease Treatment
- Review, NA, NA
*Inflam↓, *IL1β↓, *IL6↓, *IL8↓, *IL10↓, *TNF-α↓, *ROS↓, *HO-1↓, *NRF2↑, *ER Stress↓, H2O2↑,
2508- H2,    Molecular hydrogen is a promising therapeutic agent for pulmonary disease
- Review, Var, NA - Review, Sepsis, NA
*ROS↓, eff↝, *Inflam↓, *NRF2↑, *HO-1↑, *SOD↑, *Catalase↑, *MPO↑, *ASK1↓, *NADPH↓, *Sepsis↓, *HMGB1↓, ROS↑, NLRP3↑, GSDMD↑, chemoP↑, eff↑,
3770- H2,    Role of Molecular Hydrogen in Ageing and Ageing-Related Diseases
- Review, AD, NA - Review, Park, NA
*antiOx↑, *NRF2↑, *HO-1↑, *Inflam↓, *neuroP↑, *cardioP↑, *other↓, *ROS↓, *NADPH↓, *Catalase↑, *GPx1↑, *NO↓, *mt-ROS↓, *SIRT3↑, *SIRT1↑, *TLR4↓, *mTOR↓, *cognitive↑, *Sepsis↓, *PTEN↓, *Akt↓, *NLRP3↓, *AntiAg↑, *IL6↓, *TNF-α↓, *IL1β↓, *MDA↓, *memory↑, *FOXO3↑, TumCG↓, *LDL↓,

Showing Research Papers: 1 to 9 of 9

* indicates research on normal cells as opposed to diseased cells
Total Research Paper Matches: 9

Pathway results for Effect on Cancer / Diseased Cells:


NA, unassigned(tgid=0) ⓘ

CD47↓, 1,   miR-124-3p↓, 1,   PFS↑, 1,  

Redox & Oxidative Stress(tgid=1) ⓘ

H2O2↑, 1,   ROS↓, 1,   ROS↑, 3,  

Mitochondria & Bioenergetics(tgid=3) ⓘ

PGC-1α↑, 1,   XIAP↓, 1,  

Core Metabolism/Glycolysis(tgid=4) ⓘ

SCD1↓, 1,  

Cell Death(tgid=5) ⓘ

Akt↓, 2,   p‑Akt↓, 1,   Apoptosis↑, 2,   Casp3↑, 1,   GSDMD↑, 1,   IAP2/BIRC3↓, 1,   Pyro↑, 1,  

Transcription & Epigenetics(tgid=7) ⓘ

EZH2↓, 1,   other?, 1,  

Autophagy & Lysosomes(tgid=9) ⓘ

TumAuto↑, 1,  

Cell Cycle & Senescence(tgid=11) ⓘ

CDK4↓, 1,  

Proliferation, Differentiation & Cell State(tgid=12) ⓘ

PI3K↓, 1,   p‑PI3K↓, 1,   TumCG↓, 2,   Wnt↓, 1,  

Migration(tgid=13) ⓘ

Ki-67↓, 1,   MALAT1↓, 1,   TumCI↓, 1,   TumCMig↓, 1,   TumCP↓, 1,   β-catenin/ZEB1↓, 1,  

Angiogenesis & Vasculature(tgid=14) ⓘ

Hif1a↓, 1,   VEGF↓, 2,  

Immune & Inflammatory Signaling(tgid=16) ⓘ

Inflam↑, 1,   NK cell↑, 1,  

Protein Aggregation(tgid=19) ⓘ

NLRP3↑, 2,  

Hormonal & Nuclear Receptors(tgid=20) ⓘ

CDK6↑, 1,  

Drug Metabolism & Resistance(tgid=21) ⓘ

ChemoSen↑, 4,   Dose↝, 2,   eff↑, 5,   eff↝, 2,   selectivity↑, 3,  

Clinical Biomarkers(tgid=22) ⓘ

EZH2↓, 1,   GutMicro↑, 1,   Ki-67↓, 1,  

Functional Outcomes(tgid=23) ⓘ

Appetite↑, 1,   chemoP↑, 5,   cognitive↑, 1,   NP/CIPN↓, 1,   Pain↓, 1,   QoL↑, 3,   radioP↑, 4,   Sleep↑, 1,   TumVol↓, 2,   TumW↓, 1,  

Infection & Microbiome(tgid=24) ⓘ

CD8+↑, 2,  
Total Targets: 55

Pathway results for Effect on Normal Cells:


NA, unassigned(tgid=0) ⓘ

compII↑, 1,   SpO2↑, 1,   Stroke↓, 1,  

Redox & Oxidative Stress(tgid=1) ⓘ

antiOx↑, 5,   Catalase↑, 5,   Fenton↓, 1,   GPx↑, 2,   GPx1↑, 1,   HO-1↓, 1,   HO-1↑, 8,   lipid-P↓, 1,   MDA↓, 3,   MPO↓, 2,   MPO↑, 1,   NOX4↓, 1,   NRF2↑, 8,   RNS↓, 1,   ROS↓, 8,   mt-ROS↓, 1,   SIRT3↑, 1,   SOD↑, 5,   TBARS↓, 1,   VitE↓, 1,  

Mitochondria & Bioenergetics(tgid=3) ⓘ

ATP↑, 1,   compIII↑, 1,   MMP↑, 1,  

Core Metabolism/Glycolysis(tgid=4) ⓘ

ALAT↓, 1,   AMPK↑, 1,   LDL↓, 2,   NADPH↓, 4,   SIRT1↑, 2,  

Cell Death(tgid=5) ⓘ

Akt↓, 1,   Akt↑, 2,   Apoptosis↓, 2,   ASK1↓, 1,   Bax:Bcl2↓, 1,   Bcl-2↑, 1,   Bcl-xL↑, 1,   Casp12↓, 1,   Casp3↓, 1,   cl‑Casp8↑, 1,   Casp9↓, 1,   GranB/GZMB↓, 1,   p‑JNK↓, 1,   p38↓, 1,  

Transcription & Epigenetics(tgid=7) ⓘ

other↓, 1,   other↑, 1,   other↝, 1,   tumCV↓, 1,  

Protein Folding & ER Stress(tgid=8) ⓘ

CHOP/DDIT3↓, 1,   p‑eIF2α↓, 1,   ER Stress↓, 2,   GRP78/BiP↓, 1,   XBP-1↓, 1,  

Autophagy & Lysosomes(tgid=9) ⓘ

LC3‑Ⅱ/LC3‑Ⅰ↑, 1,  

DNA Damage & Repair(tgid=10) ⓘ

DNAdam↓, 1,  

Proliferation, Differentiation & Cell State(tgid=12) ⓘ

FOXO3↑, 1,   mTOR↓, 2,   p‑mTOR↓, 1,   PI3K↑, 2,   PTEN↓, 1,   STAT3↑, 1,  

Migration(tgid=13) ⓘ

AntiAg↑, 1,   APP↓, 1,   TGF-β↑, 1,   Treg lymp↝, 1,   TumCI↓, 1,   TumCMig↓, 1,   TumCP↓, 1,  

Angiogenesis & Vasculature(tgid=14) ⓘ

ATF4↓, 1,   NO↓, 1,  

Barriers & Transport(tgid=15) ⓘ

BBB↑, 1,   IBI↑, 1,  

Immune & Inflammatory Signaling(tgid=16) ⓘ

CD25+↑, 1,   CD4+↑, 2,   FOXP3↑, 1,   HMGB1↓, 2,   IFN-γ↓, 1,   IL10↓, 1,   IL10↑, 2,   IL1β↓, 5,   IL2↓, 1,   IL4↓, 2,   IL4↑, 1,   IL6↓, 8,   IL8↓, 1,   Imm↑, 1,   Inflam↓, 8,   JAK2↑, 1,   LPS↓, 1,   M2 MC↑, 1,   MCP1/CCL2↓, 1,   NF-kB↓, 3,   PGE2↓, 1,   TLR4↓, 1,   TNF-α↓, 8,  

Cellular Microenvironment(tgid=17) ⓘ

NOX↓, 1,  

Protein Aggregation(tgid=19) ⓘ

Aβ↓, 1,   BACE/β-secretase↓, 1,   NLRP3↓, 5,  

Drug Metabolism & Resistance(tgid=21) ⓘ

BioAv↝, 1,   Dose↓, 1,   Dose↑, 1,   Dose↝, 3,   eff↑, 2,   Half-Life↓, 1,   selectivity↑, 1,  

Clinical Biomarkers(tgid=22) ⓘ

ALAT↓, 1,   AST↓, 1,   creat↓, 1,   GutMicro↑, 1,   IL6↓, 8,   Urea↓, 1,  

Functional Outcomes(tgid=23) ⓘ

antiPs↑, 1,   cardioP↑, 3,   chemoP↑, 2,   cognitive↑, 2,   hepatoP↑, 3,   memory↑, 1,   neuroP↑, 4,   Obesity↓, 1,   OS↑, 1,   radioP↑, 1,   RenoP↑, 2,   Weight↑, 1,  

Infection & Microbiome(tgid=24) ⓘ

Sepsis↓, 5,  
Total Targets: 126

Scientific Paper Hit Count for: HO-1, HMOX1
9 Hydrogen Gas
Query results interpretion may depend on "conditions" listed in the research papers.
Such Conditions may include : 
  -low or high Dose
  -format for product, such as nano of lipid formations
  -different cell line effects
  -synergies with other products 
  -if effect was for normal or cancerous cells

Filter Conditions: Pro/AntiFlg:%  IllCat:%  CanType:%  Cells:%  prod#:295  Target#:597  State#:%  Dir#:%
  wNotes=0  sortOrder:rid,rpid

 

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