Database Query Results : , , SNCG

SNCG, SNCG gene: Click to Expand ⟱
Source:
Type:
SNCG gene, also known as the synuclein gamma gene, is a gene that encodes a protein called synuclein gamma. This protein is a member of the synuclein family, which also includes alpha-synuclein and beta-synuclein.

The SNCG gene is located on chromosome 10q23 and is expressed in various tissues, including the brain, breast, and other organs. The synuclein gamma protein is involved in several cellular processes, including cell signaling, cell growth, and cell survival.

Dysregulation of the SNCG gene has been implicated in several types of cancer, including breast cancer, ovarian cancer, and neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease.

In cancer, overexpression of the SNCG gene has been associated with tumor progression, metastasis, and poor prognosis.


Scientific Papers found: Click to Expand⟱
422- CUR,    Curcumin induces re-expression of BRCA1 and suppression of γ synuclein by modulating DNA promoter methylation in breast cancer cell lines
- in-vitro, BC, HCC-38 - in-vitro, BC, T47D
BRCA1↑, TET1↑, DNMT3A↑, DNMT1↓, SNCG↓, miR-29b↓, miR-29b↑,

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

Pathway results for Effect on Cancer / Diseased Cells:


DNA Damage & Repair

BRCA1↑, 1,   DNMT1↓, 1,   DNMT3A↑, 1,  

Migration

miR-29b↓, 1,   miR-29b↑, 1,   TET1↑, 1,  

Protein Aggregation

SNCG↓, 1,  

Clinical Biomarkers

BRCA1↑, 1,  
Total Targets: 8

Pathway results for Effect on Normal Cells:


Total Targets: 0

Scientific Paper Hit Count for: SNCG, SNCG gene
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#:659  State#:%  Dir#:%
wNotes=0 sortOrder:rid,rpid

 

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