AMPK Cancer Research Results
AMPK, adenosine monophosphate-activated protein kinase: Click to Expand ⟱
| Source: |
| Type: |
AMPK: guardian of metabolism and mitochondrial homeostasis; Upon changes in the ATP-to-AMP ratio, AMPK is activated. (AMPK) is a key metabolic sensor that is pivotal for the maintenance of cellular energy homeostasis. It is well documented that AMPK possesses a suppressor role in the context of tumor development and progression by modulating the inflammatory and metabolic pathways.
-Activating AMPK can inhibit anabolic processes and the PI3K/Akt/mTOR pathway reducing glycolysis shifting toward Oxidative Phosphorlylation.
AMPK activators:
-metformin or AICAR
-Resveratrol: activate AMPK indirectly
-Berberine
-Quercetin: may stimulate AMPK
-EGCG: thought to activate AMPK
-Curcumin: may activate AMPK
-Ginsenosides: Some ginsenosides have been associated with AMPK activation
-Beta-Lapachone: A natural naphthoquinone compound found in the bark of Tabebuia avellanedae (also known as lapacho or taheebo). It has been observed to activate AMPK in certain models.
-Alpha-Lipoic Acid (ALA): associated with AMPK activation
|
Bladder, Bladder Cancer: Click to Expand ⟱
Scientific Papers found: Click to Expand⟱
| - |
in-vitro, |
Bladder, |
T24/HTB-9 |
|
|
|
tumCV↓, TumCP↓, TumCMig↓, Casp↑, TumAuto↑, LC3B-II↑, p‑AMPK↑, mTOR↓, BMI1↓, ROS↑, eff↓,
| - |
in-vitro, |
CRC, |
T24/HTB-9 |
|
|
|
- |
in-vitro, |
Nor, |
SV-HUC-1 |
|
|
|
- |
in-vitro, |
Bladder, |
5637 |
|
|
|
- |
in-vivo, |
NA, |
NA |
|
|
|
HDAC↓, AntiTum↑, TumCMig↓, AMPK↑, mTOR↑, TumAuto↑, ROS↑, miR-139-5p↑, BMI1↓, TumCI?, E-cadherin↑, N-cadherin↓, Vim↓, Snail↓, cl‑PARP↑, cl‑Casp3↑, BAX↑, Bcl-2↓, Bcl-xL↓, MMP↓, PINK1↑, PARK2↑, TumMeta↓, TumCG↓, LC3II↑, p62↓, eff↓,
| - |
in-vitro, |
Bladder, |
T24/HTB-9 |
|
|
|
tumCV↓, ROS↑, AMPK↑, Glycolysis↓, p‑PI3K↓, p‑Akt↓, Casp↑, mTOR↓, ACC↓, FASN↓,
| - |
in-vitro, |
Bladder, |
T24/HTB-9 |
|
|
|
- |
in-vitro, |
BC, |
UMUC3 |
|
|
|
PKM2↓, p‑STAT3↓, TumCG↓, eff↑, chemoP↑, AMPK↑,
| - |
in-vitro, |
Bladder, |
T24/HTB-9 |
|
|
|
- |
in-vitro, |
Bladder, |
J82 |
|
|
|
Glycolysis↑, GlucoseCon↑, lactateProd↑, TCA↓, PI3K↑, Akt↑, AMPK↑, mTORC1↓, TumAuto↑, GLUT1↑, HK2↑, LDHA↑, ACC↓, PDH↓, eff↓, cMyc↓, Hif1a↑, p‑Akt↑, eff↓, eff↓, eff↓, eff↓, ROS↑,
Showing Research Papers: 1 to 5 of 5
* indicates research on normal cells as opposed to diseased cells
Total Research Paper Matches: 5
Pathway results for Effect on Cancer / Diseased Cells:
Redox & Oxidative Stress(tgid=1) ⓘ
PARK2↑, 1, ROS↑, 4,
Mitochondria & Bioenergetics(tgid=3) ⓘ
MMP↓, 1, PINK1↑, 1,
Core Metabolism/Glycolysis(tgid=4) ⓘ
ACC↓, 2, AMPK↑, 4, p‑AMPK↑, 1, cMyc↓, 1, FASN↓, 1, GlucoseCon↑, 1, Glycolysis↓, 1, Glycolysis↑, 1, HK2↑, 1, lactateProd↑, 1, LDHA↑, 1, PDH↓, 1, PKM2↓, 1, TCA↓, 1,
Cell Death(tgid=5) ⓘ
Akt↑, 1, p‑Akt↓, 1, p‑Akt↑, 1, BAX↑, 1, Bcl-2↓, 1, Bcl-xL↓, 1, Casp↑, 2, cl‑Casp3↑, 1,
Transcription & Epigenetics(tgid=7) ⓘ
tumCV↓, 2,
Autophagy & Lysosomes(tgid=9) ⓘ
LC3B-II↑, 1, LC3II↑, 1, p62↓, 1, TumAuto↑, 3,
DNA Damage & Repair(tgid=10) ⓘ
cl‑PARP↑, 1,
Proliferation, Differentiation & Cell State(tgid=12) ⓘ
BMI1↓, 2, HDAC↓, 1, mTOR↓, 2, mTOR↑, 1, mTORC1↓, 1, PI3K↑, 1, p‑PI3K↓, 1, p‑STAT3↓, 1, TumCG↓, 2,
Migration(tgid=13) ⓘ
E-cadherin↑, 1, miR-139-5p↑, 1, N-cadherin↓, 1, Snail↓, 1, TumCI?, 1, TumCMig↓, 2, TumCP↓, 1, TumMeta↓, 1, Vim↓, 1,
Angiogenesis & Vasculature(tgid=14) ⓘ
Hif1a↑, 1,
Barriers & Transport(tgid=15) ⓘ
GLUT1↑, 1,
Drug Metabolism & Resistance(tgid=21) ⓘ
eff↓, 7, eff↑, 1,
Functional Outcomes(tgid=23) ⓘ
AntiTum↑, 1, chemoP↑, 1,
Total Targets: 56
Pathway results for Effect on Normal Cells:
Total Targets: 0
Scientific Paper Hit Count for: AMPK, adenosine monophosphate-activated protein kinase
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:32 Cells:% prod#:% Target#:9 State#:% Dir#:2
wNotes=0 sortOrder:rid,rpid
Home Page