angioG Cancer Research Results

angioG, angiogenesis: Click to Expand ⟱
Source:
Type:
Process through which new blood vessels.
Angiogenesis, the process of new blood vessel formation from pre-existing vessels, plays a crucial role in cancer progression and metastasis. Tumors require a blood supply to grow beyond a certain size and to spread to other parts of the body.
Vascular Endothelial Growth Factor (VEGF): VEGF is one of the most important pro-angiogenic factors. It stimulates endothelial cell proliferation and migration, leading to the formation of new blood vessels. Many tumors overexpress VEGF, which correlates with poor prognosis.
Hypoxia-Inducible Factor (HIF): In response to low oxygen levels (hypoxia), tumors can activate HIF, which in turn promotes the expression of VEGF and other angiogenic factors. This mechanism allows tumors to adapt to their microenvironment and sustain growth.
-Tumour development and progression beyond a size of few millimetres‐cubed crucially depends on the onset of angiogenesis, that is, the ‘angiogenic switch’


AML, Acute Myeloid Leukemia: Click to Expand ⟱
Acute Myeloid Leukemia

Scientific Papers found: Click to Expand⟱
5634- BCA,    Molecular Mechanisms of Biochanin A in AML Cells: Apoptosis Induction and Pathway-Specific Regulation in U937 and THP-1
- in-vitro, AML, U937 - in-vitro, AML, THP1
Apoptosis↑, Casp7↑, PARP1↑, Bcl-2↓, Myc↓, CHOP/DDIT3↑, P21↑, p62↑, TumCCA↑, TXNIP↑, ROS↑, *antiOx↑, *Inflam↓, *neuroP↑, AntiCan↑, TumCP↓, angioG↓, TumMeta↓, VEGF↓, MMPs↓, tumCV↓, DNAdam↑, CHOP/DDIT3↑, cMyc↓, BioAv↓, Half-Life↓, BioAv↑,
3182- SFN,    Sulforaphane Modulates AQP8-Linked Redox Signalling in Leukemia Cells
- in-vitro, AML, NA
Prx↓, AQPs↓, NOX↓, tumCV↓, AntiCan↑, cardioP↑, neuroP↑, Inflam↓, chemoPv↑, angioG↓, TumMeta↓, selectivity↑, ROS↓,

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:


Redox & Oxidative Stress(tgid=1)

Prx↓, 1,   ROS↓, 1,   ROS↑, 1,  

Core Metabolism/Glycolysis(tgid=4)

cMyc↓, 1,  

Cell Death(tgid=5)

Apoptosis↑, 1,   Bcl-2↓, 1,   Casp7↑, 1,   Myc↓, 1,  

Transcription & Epigenetics(tgid=7)

tumCV↓, 2,  

Protein Folding & ER Stress(tgid=8)

CHOP/DDIT3↑, 2,  

Autophagy & Lysosomes(tgid=9)

p62↑, 1,  

DNA Damage & Repair(tgid=10)

DNAdam↑, 1,   PARP1↑, 1,  

Cell Cycle & Senescence(tgid=11)

P21↑, 1,   TumCCA↑, 1,  

Migration(tgid=13)

MMPs↓, 1,   TumCP↓, 1,   TumMeta↓, 2,   TXNIP↑, 1,  

Angiogenesis & Vasculature(tgid=14)

angioG↓, 2,   VEGF↓, 1,  

Barriers & Transport(tgid=15)

AQPs↓, 1,  

Immune & Inflammatory Signaling(tgid=16)

Inflam↓, 1,  

Cellular Microenvironment(tgid=17)

NOX↓, 1,  

Drug Metabolism & Resistance(tgid=21)

BioAv↓, 1,   BioAv↑, 1,   Half-Life↓, 1,   selectivity↑, 1,  

Clinical Biomarkers(tgid=22)

Myc↓, 1,  

Functional Outcomes(tgid=23)

AntiCan↑, 2,   cardioP↑, 1,   chemoPv↑, 1,   neuroP↑, 1,  
Total Targets: 33

Pathway results for Effect on Normal Cells:


Redox & Oxidative Stress(tgid=1)

antiOx↑, 1,  

Immune & Inflammatory Signaling(tgid=16)

Inflam↓, 1,  

Functional Outcomes(tgid=23)

neuroP↑, 1,  
Total Targets: 3

Scientific Paper Hit Count for: angioG, angiogenesis
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:2  Cells:%  prod#:%  Target#:447  State#:%  Dir#:1
wNotes=0 sortOrder:rid,rpid

 

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