GSDMD Cancer Research Results
GSDMD, gasdermin D: Click to Expand ⟱
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GSDMD is best known for its central role in mediating pyroptosis, a form of inflammatory programmed cell death.
-Some studies suggest that increased GSDMD expression and associated pyroptosis may improve local antitumor immunity.
-Some preclinical studies indicate that enhanced pyroptosis via GSDMD activation may correlate with a better prognosis, likely through improved immune-mediated clearance of tumor cells.
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Scientific Papers found: Click to Expand⟱
*diuretic↑, diuretic, vasorelaxant, anti-bacterial, anti-viral, anti-ulcerogenic, anti-inflammatory, and anti-cancer effects.
*Bacteria↓,
*AntiViral↑,
*Inflam↓,
AntiCan↑,
*cardioP↑, timely overview of emodin related to the treatment of cardiovascular disease.
*NF-kB↓, graphic abstract Immunomoduation
*TNF-α↓,
*IL1β↓,
*NO↑,
*eNOS↑,
*PPARγ↑,
*Casp9↓, anti-apoptosis
*Casp3↓,
*GSDMD↓,
*Bcl-2↑,
*STAT3↑,
*ATP↑, anti-oxidant
*SOD↑,
*GSH↑,
*HDAC2↓, anti cardiac hypertrophy
*SIRT3↑,
ROS↑, anti-proliferative
PCNA↓,
P53↑,
cMyc↓,
*BMD↑, PEMF increased the bone mineral density of the proximal femur and L5 vertebral body and improved parameters of the proximal tibia and L4 vertebral body.
*NLRP3↓, PEMF also dramatically inhibited NLRP3-mediated low-grade inflammation in the bone marrow,
*proCasp1↓, PEMF inhibited the levels of NLRP3, proCaspase1, cleaved Caspase1, IL-1β, and GSDMD-N.
*cl‑Casp1↓,
*IL1β↓,
*GSDMD↓,
*mt-ROS↓, quercetin treatment downregulated redox status, lipid droplets, and LPO release, restored damaged mitochondrial membrane potential, and repaired mtDNA damage, PGC-1α nuclear transfer, and mitochondrial dynamics.
*lipid-P↓,
*MMP↑,
*mtDam↓,
*NLRP3↓, gene and protein expressions of NLRP3, ASC, cleaved-caspase1, IL-18, IL-1β, and GSDMD-N were decreased, which effectively inhibited cell pyroptosis.
*ASC↓,
*cl‑Casp1↓,
*IL18↓,
*IL1β↓,
*GSDMD↓,
*Pyro↓,
*CYP2E1↓, Quercetin Inhibited CYP2E1 Activity to Alleviate High-Concentration Ethanol-Induced Hepatocyte Oxidative Stress and Lipid Peroxidation
*MFN1↓, Our study found that quercetin inhibited the expressions of mitochondrial fusion genes including Mfn1, Mfn2, and OPA1,
*MFN2↓,
*OPA1↓,
*DRP1/DNM1L↑, as well as increased fission genes expressions, and and the most significant change was Drp1
Showing Research Papers: 1 to 3 of 3
* indicates research on normal cells as opposed to diseased cells
Total Research Paper Matches: 3
Pathway results for Effect on Cancer / Diseased Cells:
Redox & Oxidative Stress(tgid=1) ⓘ
ROS↑, 1,
Core Metabolism/Glycolysis(tgid=4) ⓘ
cMyc↓, 1,
DNA Damage & Repair(tgid=10) ⓘ
P53↑, 1, PCNA↓, 1,
Functional Outcomes(tgid=23) ⓘ
AntiCan↑, 1,
Total Targets: 5
Pathway results for Effect on Normal Cells:
NA, unassigned(tgid=0) ⓘ
diuretic↑, 1,
Redox & Oxidative Stress(tgid=1) ⓘ
CYP2E1↓, 1, GSH↑, 1, lipid-P↓, 1, MFN1↓, 1, MFN2↓, 1, OPA1↓, 1, mt-ROS↓, 1, SIRT3↑, 1, SOD↑, 1,
Mitochondria & Bioenergetics(tgid=3) ⓘ
ATP↑, 1, DRP1/DNM1L↑, 1, MMP↑, 1, mtDam↓, 1,
Core Metabolism/Glycolysis(tgid=4) ⓘ
PPARγ↑, 1,
Cell Death(tgid=5) ⓘ
Bcl-2↑, 1, cl‑Casp1↓, 2, proCasp1↓, 1, Casp3↓, 1, Casp9↓, 1, GSDMD↓, 3, Pyro↓, 1,
Proliferation, Differentiation & Cell State(tgid=12) ⓘ
HDAC2↓, 1, STAT3↑, 1,
Angiogenesis & Vasculature(tgid=14) ⓘ
eNOS↑, 1, NO↑, 1,
Immune & Inflammatory Signaling(tgid=16) ⓘ
ASC↓, 1, IL18↓, 1, IL1β↓, 3, Inflam↓, 1, NF-kB↓, 1, TNF-α↓, 1,
Protein Aggregation(tgid=19) ⓘ
NLRP3↓, 2,
Clinical Biomarkers(tgid=22) ⓘ
BMD↑, 1,
Functional Outcomes(tgid=23) ⓘ
cardioP↑, 1,
Infection & Microbiome(tgid=24) ⓘ
AntiViral↑, 1, Bacteria↓, 1,
Total Targets: 37
Scientific Paper Hit Count for: GSDMD, gasdermin D
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#:1317 State#:% Dir#:1
wNotes=on sortOrder:rid,rpid
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