TumVol Cancer Research Results
TumVol, Tumor Volume: Click to Expand ⟱
| Source: |
| Type: |
Tumor Volume
|
Scientific Papers found: Click to Expand⟱
tumCV↓, Berbamine suppressed the cell viability of CRC cells in concentration-dependent and time-dependent manners.
TumCCA↑, berbamine increased cell apoptotic rate and induced cell cycle arrest at G0/G1 phase.
MMP↓, Berbamine treatment also decreased the mitochondrial membrane potential in CRC cells.
P53↑, berbamine increased the protein levels of p53, caspase-3, caspase-9, Bax and poly ADP ribose polymerase, and decreased the protein levels of Bcl-2 in CRC cells.
Casp3↑,
Casp9↑,
BAX↑,
PARP↑,
Bcl-2↓,
TumVol↑, Tumor growth by grafted SW480 cells were significantly suppressed in berbamine group.
| - |
vitro+vivo, |
MG, |
U87MG |
|
|
|
- |
vitro+vivo, |
MG, |
T98G |
|
|
|
HH↓, Both mRNA and protein levels of SHH/GLI1 signaling (Shh, Smo, GLI1) were downregulated in a dose‐ and time‐dependent manner
Shh↓, inhibition of SHH/GLI1 signaling by curcumin may act as a novel mechanism of the apoptosis.
Gli1↓,
cycD1/CCND1↓,
Bcl-2↓,
FOXM1↓,
Bax:Bcl2↑, The Bax/Bcl‐2 ratio (Figure 6D) also gradually increased.
TumCP↓, Curcumin suppressed cell proliferation, colony formation, migration, and induced apoptosis which was mediated partly through the mitochondrial pathway after an increase in the ratio of Bax to Bcl2.
TumCMig↓,
Apoptosis↑,
TumVol↑, Intraperitoneal injection of curcumin in vivo reduced tumor volume,
TumCCA↑, Curcumin Inhibited Proliferation of Human Glioma Cells and induced G2/M Arrest
Casp3↑, level of caspase‐3 increases significantly after curcumin treatment.
OS↑, Curcumin Inhibited GBM Growth in Vivo through SHH/GLI1 Signaling and Prolonged the Survival Period
chemoP↑, H2 plays a promising therapeutic role as an independent therapy as well as an adjuvant in combination therapy, resulting in an overall improvement in survivability, quality of life, blood parameters, and tumour reduction.
OS↑,
QoL↑,
TumVol↑,
ROS↑, Hydrogen, the lightest element on the earth, is an effective antioxidant that has been shown to selectively reduce harmful reactive oxygen species (ROS) in tissues
AntiTum↑, Although H2 has demonstrated significant anti-tumoural effects, the underlying mechanisms have not yet been elucidated.
other↝, Many studies have shown that H2 therapy can reduce oxidative stress. This, however, contradicts radiation therapy and chemotherapy, in which ROS are required to induce apoptosis and combat cancer.
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 ⓘ
ROS↑, 1,
Mitochondria & Bioenergetics ⓘ
MMP↓, 1,
Cell Death ⓘ
Apoptosis↑, 1, BAX↑, 1, Bax:Bcl2↑, 1, Bcl-2↓, 2, Casp3↑, 2, Casp9↑, 1,
Transcription & Epigenetics ⓘ
other↝, 1, tumCV↓, 1,
DNA Damage & Repair ⓘ
P53↑, 1, PARP↑, 1,
Cell Cycle & Senescence ⓘ
cycD1/CCND1↓, 1, TumCCA↑, 2,
Proliferation, Differentiation & Cell State ⓘ
FOXM1↓, 1, Gli1↓, 1, HH↓, 1, Shh↓, 1,
Migration ⓘ
TumCMig↓, 1, TumCP↓, 1,
Clinical Biomarkers ⓘ
FOXM1↓, 1,
Functional Outcomes ⓘ
AntiTum↑, 1, chemoP↑, 1, OS↑, 2, QoL↑, 1, TumVol↑, 3,
Total Targets: 26
Pathway results for Effect on Normal Cells:
Total Targets: 0
Scientific Paper Hit Count for: TumVol, Tumor Volume
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#:530 State#:% Dir#:2
wNotes=on sortOrder:rid,rpid
Home Page