ABCC2 Cancer Research Results

ABCC2, ABCC2: Click to Expand ⟱
Source:
Type:

ATP-binding cassette subfamily C member 2 (ABCC2; protein name multidrug resistance-associated protein 2, MRP2; also called cMOAT) is an ATP-dependent membrane efflux transporter. It exports organic anions, glutathione, glucuronide and sulfate conjugates, bilirubin conjugates, and several therapeutic drugs from cells. In cancer, ABCC2/MRP2 ↑ is commonly associated with increased drug efflux, reduced intracellular drug accumulation, and chemotherapy resistance. Conversely, ABCC2/MRP2 ↓ or transporter inhibition generally increases intracellular drug exposure and may restore treatment sensitivity. The direction should be interpreted according to the cancer type and whether the administered drug is an ABCC2 substrate. Gene reference; Cancer drug-resistance review.



Scientific Papers found: Click to Expand⟱
6975- Form,    Formononetin inhibits colorectal cancer via the miR-490-3p/ABCC2 axis and synergizes with 5-fluorouracil: mechanistic insights and therapeutic implications
- vitro+vivo, CRC, NA
TumCP↓, MRP↓, miR-490↑, eff⇅, ChemoSen↑, ABCC2↓,

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:


NA, unassigned(tgid=0)

ABCC2↓, 1,   miR-490↑, 1,  

Migration(tgid=13)

TumCP↓, 1,  

Barriers & Transport(tgid=15)

MRP↓, 1,  

Drug Metabolism & Resistance(tgid=21)

ChemoSen↑, 1,   eff⇅, 1,  
Total Targets: 6

Pathway results for Effect on Normal Cells:


Total Targets: 0

Scientific Paper Hit Count for: ABCC2, ABCC2
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#:1545  State#:%  Dir#:1
wNotes=0 sortOrder:rid,rpid

 

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