Evodiamine / cycD1/CCND1 Cancer Research Results

EVO, Evodiamine: Click to Expand ⟱
Features:
Evodiamine is a bioactive alkaloid isolated primarily from the fruit of the traditional Chinese medicinal herb Evodia rutaecarpa. Evodiamine is a natural alkaloid from Evodia rutaecarpa, a traditional Chinese medicine. It has various pharmacological activities, such as anti-inflammatory, anti-cancer, anti-microbial and metabolic regulation, but also shows hepatotoxicity and cardiotoxicity.

Evodiamine — a naturally occurring quinazolinocarboline indole alkaloid isolated mainly from the dried, immature fruit of Tetradium ruticarpum, historically known as Evodia rutaecarpa or Evodiae Fructus. It is classified as an experimental plant-derived small molecule and multitarget anticancer lead compound. Standard abbreviations include EVO, EVD and EDM. Evodiamine interacts with topoisomerases, microtubules, mitochondrial death pathways and several oncogenic signalling networks, but it is not an approved anticancer drug and has extremely poor oral bioavailability.

Primary mechanisms (ranked):

  1. Disruption of DNA topology through inhibition or trapping of topoisomerase I and catalytic inhibition of topoisomerase II, producing replication stress, DNA damage signalling and cell-cycle arrest.
  2. Mitotic disruption through altered tubulin polymerization and microtubule dynamics, commonly producing G2/M or mitotic arrest.
  3. Induction of mitochondrial and endoplasmic-reticulum-associated apoptosis through mitochondrial membrane depolarization, Bax/Bcl-2 modulation, cytochrome-c release and caspase activation.
  4. Suppression of PI3K/AKT/mTOR and related survival signalling, with context-dependent activation of stress MAPKs including JNK and p38.
  5. ROS elevation and oxidative stress that amplify mitochondrial dysfunction, DNA damage and apoptosis in susceptible cancer cells.
  6. Suppression of NF-κB and STAT3 transcriptional signalling, reducing anti-apoptotic, inflammatory, angiogenic and metastatic gene expression.
  7. Inhibition of HSP70-mediated proteostasis and survival of cancer stem-like and chemoresistant cell populations.
  8. Suppression of invasion, EMT, angiogenesis and immune-evasion signalling, including context-dependent reductions in MMP-9, VEGF, MUC1-C and PD-L1.
  9. Induction of autophagy, which may be cytotoxic or cytoprotective depending on cancer type, concentration and treatment duration.

Bioavailability / PK relevance: Native evodiamine is poorly water-soluble, has limited gastrointestinal absorption, undergoes extensive metabolism and has exceptionally low systemic oral bioavailability in animal models; an approximate oral bioavailability of 0.1% has been reported in rats. Nanoparticles, phospholipid complexes, solid dispersions, liposomes and structural analogues improve exposure experimentally, but no optimized formulation has established clinical anticancer efficacy.

In-vitro vs systemic exposure relevance: Most anticancer experiments use micromolar evodiamine concentrations maintained for hours to days. These exposures substantially exceed the plasma concentrations expected after conventional oral evodiamine because of its poor dissolution, absorption and systemic availability. Direct translation of common cell-culture concentrations to oral supplementation is therefore not pharmacokinetically supported.

Clinical evidence status: Preclinical only. Anticancer evidence consists primarily of cell-culture studies, xenografts and other animal models. No established randomized clinical trial evidence demonstrates efficacy against cancer, and evodiamine has no FDA, EMA or Health Canada approval as an anticancer therapy. Hepatotoxicity, cardiotoxicity, formulation limitations and uncertain human pharmacokinetics remain major development barriers.


Evodiamine Mechanistic Profile

Rank Pathway / Axis Cancer Cells Normal Cells TSF Primary Effect Notes / Interpretation
1 Topoisomerase I and II TOP1-DNA cleavage complexes ↑; TOP1 and TOP2 activity ↓; DNA damage ↑ DNA damage possible ↑ at sufficient exposure R–G Replication stress, DNA strand damage and growth inhibition Evodiamine has been reported as a TOP1 poison or cleavage-complex stabilizer and as a dual TOP1/TOP2 catalytic inhibitor; the precise mode is assay-dependent.
2 Tubulin and mitotic progression Tubulin polymerization altered; G2/M arrest ↑; mitotic arrest ↑ Mitotic toxicity possible ↑ in proliferating normal cells R–G Failure of mitotic progression Microtubule disruption may explain the frequent G2/M phenotype better than TOP1 inhibition alone.
3 Mitochondrial apoptosis Mitochondrial membrane potential ↓; Bax ↑; Bcl-2 and Bcl-xL ↓; cytochrome c ↑; caspase-9 and caspase-3 ↑ Mitochondrial toxicity possible ↑ (dose-dependent) R–G Intrinsic apoptotic cell death One of the most consistently reproduced downstream effects across cancer models.
4 PI3K AKT mTOR survival signalling PI3K ↓; p-AKT ↓; mTOR signalling ↓ Variable or insufficiently characterized R–G Reduced survival, proliferation and therapy resistance Observed in glioma, pancreatic, hepatic, prostate and other cancer models; not necessarily a direct molecular target.
5 Mitochondrial ROS and oxidative stress ROS ↑; oxidative damage ↑; mitochondrial dysfunction ↑ Oxidative injury possible ↑ at toxic concentrations P–R Amplification of apoptosis and cell-cycle arrest ROS dependence is model-dependent; antioxidant rescue has been reported in selected systems. This is not evidence of cancer-selective oxidative stress in humans.
6 Stress MAPK signalling JNK ↑; p38 ↑; ERK variable Variable or insufficiently characterized P–R Stress signalling, mitotic arrest and apoptosis MAPK direction varies by cell type and exposure; JNK activation is mechanistically important in several colorectal and mitochondrial-apoptosis models.
7 NF-κB inflammatory and survival signalling IKK activity ↓; IκBα degradation ↓; NF-κB activation ↓; COX-2 ↓; anti-apoptotic proteins ↓ Inflammatory signalling ↓ (context-dependent) R–G Reduced survival, inflammation, invasion and chemoresistance NF-κB suppression can sensitize experimental tumors to gemcitabine and other cytotoxic treatments.
8 SHP-1 STAT3 axis SHP-1 ↑; STAT3 Tyr705 phosphorylation ↓; cyclin D1, survivin, XIAP, VEGF and MMP-9 ↓ Insufficiently characterized R–G Reduced proliferation, angiogenesis and survival Strongly demonstrated in hepatocellular carcinoma models but may not generalize uniformly across cancers.
9 HSP70 proteostasis HSP70 function ↓; proteotoxic stress ↑; cancer stem-cell survival ↓ Potential proteostasis toxicity (dose-dependent) R–G Apoptosis of bulk, stem-like and drug-resistant cancer populations HSP70 has been proposed as a direct functional target, providing a potential mechanism against chemoresistant subpopulations.
10 Autophagy LC3-II and autophagosome formation ↑ Insufficiently characterized G Context-dependent cell death or survival adaptation Autophagy may contribute to cytotoxicity in some models but protect tumor cells in others; combination with autophagy inhibition can enhance activity experimentally.
11 EMT invasion and angiogenesis EMT ↓; MMP-2 and MMP-9 ↓; VEGF ↓; migration and invasion ↓ Endothelial angiogenic activity may ↓ G Reduced metastatic and angiogenic phenotype Primarily preclinical and often secondary to suppression of NF-κB, STAT3, AKT or β-catenin signalling.
12 MUC1-C PD-L1 immune-evasion axis MUC1-C ↓; PD-L1 ↓; CD8-positive T-cell activity ↑ in immunocompetent models Normal immune effects uncertain G Reduced immune evasion Promising but model-specific evidence; no clinical immunotherapy combination data are available.
13 Chemosensitization Resistance signalling ↓; apoptosis with gemcitabine, erlotinib or other agents ↑ Combination toxicity uncertain G Enhanced experimental treatment response Combination effects remain preclinical and cannot currently support adjunct use in patients.
14 Clinical Translation Constraint Systemic exposure after oral dosing very low Hepatic and cardiac injury possible; CYP-mediated interactions possible G Limits clinical feasibility and therapeutic index Poor solubility, approximately 0.1% rat oral bioavailability, extensive metabolism, uncertain human dosing, hepatotoxicity and cardiotoxicity prevent direct translation of micromolar in-vitro findings.

P: 0–30 min    R: 30 min–3 hr    G: >3 hr
cycD1/CCND1, cyclin D1 pathway: Click to Expand ⟱
Source:
Type:
Also called CCND1 Gatekeeper of Cell-Cycle Commitment
The main function of cyclin D1 is to maintain cell cycle and to promote cell proliferation. Cyclin D1 is a key regulatory protein involved in the cell cycle, particularly in the transition from the G1 phase to the S phase. It is part of the cyclin-dependent kinase (CDK) complex, where it binds to CDK4 or CDK6 to promote cell cycle progression.
Cyclin D1 is crucial for the regulation of the cell cycle. Overexpression or dysregulation of cyclin D1 can lead to uncontrolled cell proliferation, a hallmark of cancer.
Cyclin D1 is often found to be overexpressed in various cancers.
Cyclin D1 can interact with tumor suppressor proteins, such as retinoblastoma (Rb). When cyclin D1 is overexpressed, it can lead to the phosphorylation and inactivation of Rb, releasing E2F transcription factors that promote the expression of genes required for DNA synthesis and cell cycle progression.
Cyclin D1 is influenced by various signaling pathways, including the PI3K/Akt and MAPK pathways, which are often activated in cancer.
In some cancers, high levels of cyclin D1 expression have been associated with poor prognosis, making it a potential biomarker for cancer progression and treatment response.
Scientific Papers found: Click to Expand⟱
1057- EVO,    Evodiamine abolishes constitutive and inducible NF-kappaB activation by inhibiting IkappaBalpha kinase activation, thereby suppressing NF-kappaB-regulated antiapoptotic and metastatic gene expression, up-regulating apoptosis, and inhibiting invasion
NF-kB↓, TNF-α↓, COX2/PTGS2↓, cycD1/CCND1↓, cMyc↓, MMP9↓, ICAM-1↓, MDR1↓, XIAP↓, Bcl-2↓, Bcl-xL↓, IAP1↓, IAP2/BIRC3↓, cFLIP↓, Bfl-1↓,

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:


Mitochondria & Bioenergetics(tgid=3) ⓘ

Bfl-1↓, 1,   XIAP↓, 1,  

Core Metabolism/Glycolysis(tgid=4) ⓘ

cMyc↓, 1,  

Cell Death(tgid=5) ⓘ

Bcl-2↓, 1,   Bcl-xL↓, 1,   cFLIP↓, 1,   IAP1↓, 1,   IAP2/BIRC3↓, 1,  

Cell Cycle & Senescence(tgid=11) ⓘ

cycD1/CCND1↓, 1,  

Migration(tgid=13) ⓘ

MMP9↓, 1,  

Immune & Inflammatory Signaling(tgid=16) ⓘ

COX2/PTGS2↓, 1,   ICAM-1↓, 1,   NF-kB↓, 1,   TNF-α↓, 1,  

Drug Metabolism & Resistance(tgid=21) ⓘ

MDR1↓, 1,  
Total Targets: 15

Pathway results for Effect on Normal Cells:


Total Targets: 0

Scientific Paper Hit Count for: cycD1/CCND1, cyclin D1 pathway
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#:76  Target#:73  State#:%  Dir#:%
  wNotes=0  sortOrder:rid,rpid

 

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