Recombinant Methioninase / TumCP Cancer Research Results

rMETase, Recombinant Methioninase: Click to Expand ⟱
Features:

rMETase - Recombinant Methioninase

Recommended Abbreviation: rMETase

Alternative Names: Recombinant methioninase, recombinant L-methionine α-deamino-γ-mercaptomethane lyase, recombinant methionine γ-lyase

Type: Recombinant enzyme / metabolic anticancer therapy / methionine-depleting biologic

Source: Recombinant methioninase is commonly produced from the Pseudomonas putida methioninase gene expressed in Escherichia coli.

Function: rMETase enzymatically degrades methionine and lowers extracellular and systemic methionine availability. Many cancer cells display methionine dependence or methionine addiction and therefore cannot maintain proliferation when extracellular methionine is depleted, whereas normal cells are generally more capable of compensating through methionine regeneration and related metabolic pathways.

Cancer: Preclinical studies demonstrate broad anticancer activity through methionine depletion, inhibition of proliferation, disruption of methylation-dependent metabolism, and cell-cycle arrest, frequently in late S/G2 phase. rMETase can sensitize cancer cells to chemotherapy and has shown synergistic activity with multiple cytotoxic agents in experimental tumor models.

Clinical Status: Experimental metabolic anticancer therapy. Most evidence is preclinical, although recombinant methioninase has been developed specifically for translational and clinical investigation.
TumCP, Tumor Cell proliferation: Click to Expand ⟱
Source:
Type:
Tumor cell proliferation is a key characteristic of cancer. It refers to the rapid and uncontrolled growth of cells that can lead to the formation of tumors.
Scientific Papers found: Click to Expand⟱
8052- IVM,  rMETase,    Selective Synergy of Ivermectin Combined With Recombinant Methioninase Against Colon-Cancer Cells in Contrast to Normal Fibroblasts
- in-vitro, CRC, HCT116 - in-vitro, Nor, Hs27
Dose↝, TumCP↓, selectivity↑,

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:


Migration(tgid=13) ⓘ

TumCP↓, 1,  

Drug Metabolism & Resistance(tgid=21) ⓘ

Dose↝, 1,   selectivity↑, 1,  
Total Targets: 3

Pathway results for Effect on Normal Cells:


Total Targets: 0

Scientific Paper Hit Count for: TumCP, Tumor Cell proliferation
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#:473  Target#:327  State#:%  Dir#:%
  wNotes=0  sortOrder:rid,rpid

 

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