Dysb Cancer Research Results

Dysb, Dysbiosis: Click to Expand ⟱
Source:
Type:

Dysbiosis refers to a disturbed gut microbial state characterized by reduced microbial diversity, loss of beneficial commensals, expansion of potentially pathogenic organisms, and altered production of microbial metabolites. In IBD, dysbiosis is closely linked to impaired mucosal tolerance, barrier dysfunction, exaggerated immune activation, and persistence of chronic intestinal inflammation. In cancer, especially colorectal and inflammation-associated cancer, dysbiosis may contribute to tumor initiation and progression by promoting epithelial injury, microbial translocation, genotoxic or pro-inflammatory signaling, altered bile acid and short-chain fatty acid metabolism, and an immune environment that supports carcinogenesis. Thus, dysbiosis is best viewed as a microbiome-level pathogenic factor connecting barrier failure, chronic inflammation, and cancer risk.



Scientific Papers found: Click to Expand⟱
5933- CAR,    Protective Effect of Carvacrol against Gut Dysbiosis and Clostridium difficile Associated Disease in a Mouse Model
- in-vivo, IBD, NA
*Diar↓, Carvacrol supplementation significantly reduced the incidence of diarrhea and improved the clinical and diarrhea scores in mice (p < 0.05).
*GutMicro↑, Microbiome analysis revealed a significant increase in Proteobacteria and reduction in the abundance of protective bacterial flora in antibiotic-treated and C.
*Dysb↓, Results suggest that CR could potentially be used to control gut dysbiosis and reduce C. difficile infection

6079- CHL,    Chlorophyllin Modulates Gut Microbiota and Inhibits Intestinal Inflammation to Ameliorate Hepatic Fibrosis in Mice
- in-vivo, Nor, NA
*eff↑, oral administration of chlorophyllin could attenuate intestinal and hepatic inflammation and ameliorate liver fibrosis.
*GutMicro↑, oral administration of chlorophyllin promptly rebalanced the gut microbiota, exhibiting down-regulation of the phylum Firmicutes and up-regulation of the phylum Bacteroidetes.
*NF-kB↓, chlorophyllin exposure could inhibit NF-κB pathway via IKK-phosphorylation suppression.
*MMPs↑, Chlorophyllin Treatment Increased the MMP/TIMP Ratio, Which May Promote Fibrolysis and Resolving Liver Fibrosis
*TIMP1↓,
*Inflam↓, Exposure of Intestinal Epithelial Cells With Chlorophyllin Can Attenuate Inflammatory Signaling Pathways
*Dysb↓, Dysbiosis Occurring in Liver Fibrosis Can Be Rebalanced by Oral Administration of Chlorophyllin for Eubiosis


Showing Research Papers: 1 to 2 of 2

* indicates research on normal cells as opposed to diseased cells
Total Research Paper Matches: 2

Pathway results for Effect on Cancer / Diseased Cells:


Total Targets: 0

Pathway results for Effect on Normal Cells:


NA, unassigned

Dysb↓, 2,  

Migration

MMPs↑, 1,   TIMP1↓, 1,  

Immune & Inflammatory Signaling

Inflam↓, 1,   NF-kB↓, 1,  

Drug Metabolism & Resistance

eff↑, 1,  

Clinical Biomarkers

GutMicro↑, 2,  

Infection & Microbiome

Diar↓, 1,  
Total Targets: 8

Scientific Paper Hit Count for: Dysb, Dysbiosis
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#:%  Target#:1464  State#:%  Dir#:1
wNotes=on sortOrder:rid,rpid

 

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