isoorientin / Catalase Cancer Research Results

isoO, isoorientin: Click to Expand ⟱
Features:

Isoorientin is specifically luteolin-6-C-glucoside

Isoorientin — a naturally occurring flavone C-glycoside, specifically luteolin-6-C-glucoside, also known as homoorientin. It is a dietary/plant polyphenol rather than an approved drug and occurs in multiple medicinal and food plants. Isoorientin is structurally related to orientin, but differs in the position of C-glucosylation. Its anticancer pharmacology is dominated by redox-dependent mitochondrial apoptosis and suppression of pro-survival signaling, while in non-cancer inflammatory and neurological models it generally behaves as an antioxidant and anti-inflammatory GSK3β/NF-κB modulator. This context-dependent redox behavior is important when interpreting apparently opposite ROS effects.
-buckwheat sprouts contain orientin, isoorientin, vitexin, isovitexin, and rutin

Primary mechanisms (ranked):

  1. ROS-dependent mitochondrial apoptosis in cancer cells, with mitochondrial membrane-potential loss, cytochrome-c release, Bax/Bcl-2 shift and caspase activation.
  2. PI3K/Akt survival-pathway suppression, contributing to apoptosis and reduced proliferation.
  3. MAPK/STAT3/NF-κB modulation, typically with ↑ JNK/p38 and ↓ ERK, STAT3 and NF-κB signaling in susceptible cancer models.
  4. Wnt/β-catenin/STAT3 suppression, reducing cancer stem-cell characteristics, epithelial-mesenchymal transition, invasion and tumorigenicity.
  5. AMPK activation, associated with reduced proliferation, invasiveness, EMT-associated signaling and VEGF secretion in pancreatic cancer models.
  6. Cell-cycle arrest, commonly G2/M in lung and gastric cancer models, involving ↓ cyclins/CDKs and ↑ p21/p27.
  7. Autophagy induction accompanying apoptosis in selected models, particularly HepG2 cells, through ROS-, PI3K/Akt-, JNK-, p38- and p53-linked signaling.
  8. Anti-inflammatory GSK3β inhibition with secondary NRF2/HO-1 activation in non-cancer cells; this is more relevant to neuroprotection and inflammatory disease than to the primary anticancer mechanism.

Bioavailability / PK relevance: Oral systemic exposure is low. In rats, absolute oral bioavailability was approximately 9%, with low circulating parent isoorientin after a 150 mg/kg oral dose and substantially greater formation of sulfated metabolite. Low aqueous solubility and extensive first-pass metabolism are important translational constraints. Reported intravenous terminal half-life in rats is approximately 1.7–2.1 hours.

In-vitro vs systemic exposure relevance: Many anticancer experiments use approximately 20–160 µM isoorientin, while oral administration produces low circulating parent-compound exposure. These concentrations therefore commonly exceed plausibly achievable systemic free-isoorientin concentrations after conventional oral dosing. Local gastrointestinal exposure, metabolites, high-dose experimental administration and specialized delivery systems may not follow this limitation to the same degree.

Clinical evidence status: Preclinical. Anticancer activity is supported by multiple cell studies and a small number of animal/xenograft studies, including oral squamous-cell carcinoma models. A 2026 systematic review identified 12 eligible anticancer studies but no established human oncology efficacy. Isoorientin is not an approved anticancer drug and there is no established therapeutic human cancer dose.

Isoorientin Cancer Mechanisms

Rank Pathway / Axis Cancer Cells Normal Cells TSF Primary Effect Notes / Interpretation
1 ROS-dependent mitochondrial apoptosis ↑ ROS; ↓ mitochondrial membrane potential; ↑ cytochrome c; ↑ Bax/Bcl-2 ratio; ↑ caspase-3 ↓ ROS or ↔ (context-dependent) P→G Apoptosis Core anticancer mechanism in liver, lung and gastric models. NAC substantially suppresses apoptosis, supporting a causal role for ROS rather than ROS being only a downstream marker.
2 PI3K/Akt survival signaling ↓ Akt phosphorylation; ↓ survival signaling ↔ (context-dependent) R→G Growth inhibition and apoptosis Strong mechanistic evidence in HepG2 and gastric cancer models; interacts with ROS and mitochondrial apoptosis.
3 MAPK STAT3 NF-κB signaling ↑ JNK; ↑ p38; ↓ ERK; ↓ STAT3; ↓ NF-κB ↓ excessive MAPK/NF-κB activation R→G Apoptosis and reduced pro-survival transcription ROS-dependent signaling is particularly well demonstrated in A549 lung cancer cells. In inflammatory normal-cell models, suppression of MAPK/NF-κB is predominantly cytoprotective.
4 Wnt β-catenin STAT3 and cancer stemness ↓ β-catenin; ↓ p-STAT3; ↓ TCF1/TCF7; ↓ LEF1; ↓ stemness Not established G Reduced EMT, invasion and tumor initiation Supported by oral squamous-cell carcinoma cell and xenograft models. Particularly relevant to metastatic and cancer-stem-cell phenotypes.
5 AMPK and angiogenic signaling ↑ AMPK; ↓ VEGF; ↓ invasiveness ↔ or ↑ metabolic AMPK signaling (context-dependent) R→G Growth and invasion suppression Mechanistically prominent in pancreatic cancer; PRKAA1 knockdown substantially attenuated the reported anticancer effects.
6 Cell-cycle control ↑ p21; ↑ p27; ↓ cyclin B1; ↓ CDK1/2; ↑ G2/M arrest Not established G Proliferation arrest G2/M arrest is reported in lung and gastric cancer; phase effects vary among tumor models.
7 Autophagy apoptosis coupling ↑ Beclin-1; ↑ LC3-II; ↑ autophagy Context-dependent R→G Autophagic and apoptotic cell death Best established in HepG2 cells. Pharmacologic inhibition suggests reciprocal interaction between autophagy and apoptosis rather than two independent responses.
8 EMT migration and invasion ↓ EMT; ↓ migration; ↓ invasion Not established G Antimetastatic phenotype Downstream of Wnt/β-catenin/STAT3, Akt and AMPK signaling depending on tumor model.
9 Chemosensitization ↑ cisplatin cytotoxicity (model-dependent) Not established G Potential combination therapy Demonstrated preclinically in oral squamous-cell carcinoma. Human benefit and therapeutic index remain unknown.
10 GSK3β NRF2 HO-1 inflammatory regulation Context-dependent ↓ GSK3β activity; ↑ NRF2; ↑ HO-1; ↓ NF-κB R→G Anti-inflammatory and cytoprotective activity More strongly established in macrophage, microglial and neurological disease models than as a primary cancer mechanism.
11 Clinical Translation Constraint Low oral exposure relative to many effective in-vitro concentrations Low oral exposure relative to many experimental concentrations G PK and evidence limitation Rat oral bioavailability is approximately 9%; substantial first-pass sulfation occurs. Most anticancer evidence remains cellular or animal, with no established human oncology dose or clinical efficacy.

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



Isoorientin and Alzheimer’s disease — Isoorientin has meaningful preclinical AD relevance centered on inhibition of GSK3β and suppression of neuroinflammation. In APP/PS1 mice, chronic oral administration reduced GSK3β overactivation, tau hyperphosphorylation, amyloid-β deposition and microglial inflammation while improving long-term potentiation and spatial memory. Cell studies additionally show suppression of Aβ-induced ROS, NF-κB, iNOS, COX-2 and inflammatory cytokines. This evidence remains preclinical; no established human AD efficacy or therapeutic dose has been demonstrated.

Primary mechanisms (ranked):

  1. GSK3β inhibition, reducing pathological tau phosphorylation and influencing downstream inflammatory and redox signaling.
  2. Reduction of amyloid-β-associated pathology and Aβ-induced microglial activation.
  3. NF-κB suppression with reduced TNF-α, IL-6, iNOS and COX-2.
  4. Secondary NRF2/HO-1 activation and antioxidant protection in neural and microglial cells.
  5. Protection of synaptic plasticity and cognitive function in animal models.

Clinical evidence status: Preclinical. Evidence includes cellular models and APP/PS1 transgenic mice, but there is no established clinical efficacy in human Alzheimer’s disease.

Isoorientin Alzheimer’s Mechanisms

Rank Pathway / Axis Modulation Primary Effect Notes / Interpretation
1 GSK3β ↓ activity Reduced pathological kinase signaling Isoorientin has been characterized as a substrate-competitive GSK3β inhibitor; GSK3β is a particularly relevant target because of its roles in tau phosphorylation and neuroinflammation.
2 Tau phosphorylation ↓ p-tau Reduced tau pathology Observed in APP/PS1 mouse brain and mechanistically consistent with reduced GSK3β activity.
3 Amyloid beta pathology ↓ Aβ deposition Reduced amyloid burden Reduced Aβ deposition has been reported in APP/PS1 mice; the precise contribution of direct amyloid processing versus secondary signaling effects remains uncertain.
4 Microglial NF-κB inflammation ↓ NF-κB; ↓ TNF-α; ↓ IL-6; ↓ iNOS; ↓ COX-2 Reduced neuroinflammation Supported by LPS- and Aβ-stimulated microglial models and by reduced activated microglia in APP/PS1 mice.
5 NRF2 HO-1 antioxidant response ↑ NRF2; ↑ HO-1; ↓ ROS Neuroprotection Secondary cytoprotective mechanism particularly evident in inflammatory microglial models.
6 Synaptic plasticity ↑ long-term potentiation Improved synaptic function Observed electrophysiologically in APP/PS1 mice after chronic treatment.
7 Cognition and spatial memory ↑ memory performance Functional neurological improvement Animal-model outcome; should not be interpreted as demonstrated clinical cognitive efficacy.
8 Clinical Translation Constraint Low oral bioavailability; human efficacy not established Translation limitation Animal efficacy is encouraging but human pharmacokinetics, CNS exposure, therapeutic dose and clinical effectiveness remain undetermined.


Catalase, Catalase: Click to Expand ⟱
Source:
Type:
Caspases are a cysteine protease that speed up a chemical reaction via pointing their target substrates following an aspartic acid residue.1 They are grouped into apoptotic (caspase-2, 3, 6, 7, 8, 9 and 10) and inflammatory (caspase-1, 4, 5, 11 and 12) mediated caspases.
Caspase-1 may have both tumorigenic or antitumorigenic effects on cancer development and progression, but it depends on the type of inflammasome, methodology, and cancer.
Catalase is an enzyme found in nearly all living cells exposed to oxygen. Its primary role is to protect cells from oxidative damage by catalyzing the conversion of hydrogen peroxide (H₂O₂), a potentially damaging byproduct of metabolism, into water (H₂O) and oxygen (O₂). This detoxification process is crucial because excess H₂O₂ can lead to the formation of reactive oxygen species (ROS) that damage proteins, lipids, and DNA.

Catalase and Cancer
Oxidative Stress and Cancer:
Cancer cells often experience increased levels of oxidative stress due to rapid proliferation and metabolic changes. This stress can lead to DNA damage, promoting tumorigenesis.
Catalase helps mitigate oxidative stress, and its expression can influence the survival and proliferation of cancer cells.
Expression Levels in Different Cancers:
Overexpression: In some cancers, such as breast cancer and certain types of leukemia, catalase may be overexpressed. This overexpression can help cancer cells survive in oxidative environments, potentially leading to more aggressive tumor behavior.
Downregulation: Conversely, in other cancers, such as colorectal cancer, reduced catalase expression has been observed. This downregulation can lead to increased oxidative stress, contributing to tumor progression and metastasis.
Prognostic Implications:
Survival Rates: Studies have shown that high levels of catalase expression can be associated with poor prognosis in certain cancers, as it may enable cancer cells to resist apoptosis (programmed cell death) induced by oxidative stress.

Some types of cancer cells have been reported to exhibit lower catalase activity, possibly increasing their vulnerability to oxidative damage under certain conditions. This vulnerability has even been exploited in some therapeutic strategies (for example, approaches that generate excess H₂O₂ or other ROS specifically targeting cancer cells have been researched).
Scientific Papers found: Click to Expand⟱
7883- isoO,    Evaluation of Anti-Inflammatory Properties of Isoorientin Isolated from Tubers of Pueraria tuberosa
- vitro+vivo, Nor, RAW264.7
*Inflam↓, *COX2/PTGS2↓, *TNF-α↓, *IL6↓, *5LO↓, *IL1β↓, *Catalase↑, *GSTs↑,

Showing Research Papers: 1 to 1 of 1

* indicates research on normal cells as opposed to diseased cells
Total Research Paper Matches: 1

Pathway results for Effect on Cancer / Diseased Cells:


Total Targets: 0

Pathway results for Effect on Normal Cells:


Redox & Oxidative Stress(tgid=1) ⓘ

Catalase↑, 1,   GSTs↑, 1,  

Migration(tgid=13) ⓘ

5LO↓, 1,  

Immune & Inflammatory Signaling(tgid=16) ⓘ

COX2/PTGS2↓, 1,   IL1β↓, 1,   IL6↓, 1,   Inflam↓, 1,   TNF-α↓, 1,  

Clinical Biomarkers(tgid=22) ⓘ

IL6↓, 1,  
Total Targets: 9

Scientific Paper Hit Count for: Catalase, Catalase
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#:461  Target#:46  State#:%  Dir#:2
  wNotes=0  sortOrder:rid,rpid

 

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