AQPs Cancer Research Results
AQPs, Aquaporins: Click to Expand ⟱
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Aquaporins are membrane proteins that form channels to facilitate water transport across cell membranes. They are essential for maintaining water homeostasis in various tissues, and research over the past decade has revealed their involvement in several aspects of cancer biology.
• Aquaporins can influence cell proliferation. Some studies have shown that overexpression of specific aquaporin isoforms (like AQP1, AQP3, and AQP5) is associated with increased cell proliferation in different cancer types.
-increased expression of AQP1 or AQP3 has been correlated with poor prognosis in some cancers.
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Scientific Papers found: Click to Expand⟱
*AQPs↓, Sapkota screened 2,560 compounds for the ability to increase readthrough of the aquaporin 4 gene. He found two: apigenin,
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in-vitro, |
CRC, |
HT29 |
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in-vitro, |
CRC, |
SW480 |
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in-vitro, |
CRC, |
HCT116 |
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TumCP↓, We demonstrated that treatment of these CRC cell lines with berberine inhibited cell proliferation, migration and invasion through induction of apoptosis and necrosis.
TumCMig↓,
TumCI↓,
Apoptosis↑,
necrosis↑,
AQPs↓, berberine treatment down-regulated the expression of all three types of AQPs.
PTEN↑, up-regulating PTEN and down-regulating PI3K, AKT and p-AKT expression as well as suppressing its downstream targets, mTOR and p-mTOR at the protein level
PI3K↓,
Akt↓,
p‑Akt↓,
mTOR↓,
p‑mTOR↓,
*AQPs↓, Bacopaside I (BSI), the main active compound of the herbal medicine Bacopa monnieri with anti-RA effects, inhibits tumor cell growth by blocking AQP1, but its potential use in RA is unclear.
TumCP↓, BSI suppressed proliferation, promoted apoptosis, and reduced autophagy in TNF-α-stimulated RA FLS.
Apoptosis↑,
AQPs↓, Expression of aquaporin-1 (AQP1) in endothelial cells is critical for their migration and angiogenesis in cancer. We tested the AQP1 inhibitor, bacopaside II, derived from medicinal plant Bacopa monnieri,
tumCV↓, Cell viability was reduced significantly for 2H11 at 15 μM (p = 0.037), 3B11 at 12.5 μM (p = 0.017) and HUVEC at 10 μM (p < 0.0001).
Apoptosis↑, At 15 μM, the reduced viability was accompanied by an increase in apoptosis of 38%, 50% and 32% for 2H11, 3B11 and HUVEC, respectively.
TumCMig↓, Bacopaside II at ≥10 μM significantly reduced migration of 2H11 (p = 0.0002) and 3B11 (p = 0.034).
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in-vitro, |
Colon, |
HT29 |
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in-vitro, |
Colon, |
SW48 |
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in-vitro, |
Colon, |
SW-620 |
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in-vitro, |
CRC, |
HCT116 |
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AQPs↓, Bacopa monnieri, blocks the AQP1 water channel and impairs migration of cells that express AQP1.
TumCG↓, Bacopaside II significantly reduced growth at ≥20 µM for HT-29 and ≥15 µM for SW480, SW620 and HCT116.
TumCCA↓, These results are the first to show that bacopaside II inhibits colon cancer cell growth by inducing cell cycle arrest and apoptosis.
Apoptosis↑,
eff↝, bacopaside II impaired migration of the high AQP1 expressing HT-29 but had minimal effect on the low expressing SW480,
*cognitive↑, results showed that IF ameliorated cognitive dysfunction, prevented brain from Aβ deposition, and restored the AQP4 polarity in a mouse model of AD
*Aβ↓,
*AQPs↓, IF down-regulated the expression of AQP4-M1 and histone deacetylase 3, reduced AQP4-M1/M23 ratio,
*HDAC3↓,
Prx↓, The results show that the cell treatment with 10 μM SFN for 24 h significantly decreased Prx-1 expression.
AQPs↓, Results indicated that sulforaphane inhibited both aquaporin-8 and Nox2 expression, thus decreasing B1647 cells viability.
NOX↓,
tumCV↓,
AntiCan↑, In addition to its well-known anticancer activity [2], SFN has been demonstrated to possess cardioprotective [3], neuroprotective [4], and anti-inflammatory activities
cardioP↑,
neuroP↑,
Inflam↓,
chemoPv↑, potent chemopreventive effect of SFN is based on its ability to target multiple mechanisms within the cell to control carcinogenesis
angioG↓, SFN prevents uncontrolled cancer cell proliferation through the modulation of genes involved in apoptosis and cell cycle arrest [5, 8], angiogenesis [9, 10], and metastasis
TumMeta↓,
selectivity↑, SFN is able to selectively exert cytotoxic effects in many human cancer cells without affecting normal cells
ROS↓, Results in Figure 4 show that only 10 μM SFN treatment causes a significant decrease of ROS intracellular levels in respect to control cells,
Showing Research Papers: 1 to 7 of 7
* indicates research on normal cells as opposed to diseased cells
Total Research Paper Matches: 7
Pathway results for Effect on Cancer / Diseased Cells:
Redox & Oxidative Stress ⓘ
Prx↓, 1, ROS↓, 1,
Cell Death ⓘ
Akt↓, 1, p‑Akt↓, 1, Apoptosis↑, 4, necrosis↑, 1,
Transcription & Epigenetics ⓘ
tumCV↓, 2,
Cell Cycle & Senescence ⓘ
TumCCA↓, 1,
Proliferation, Differentiation & Cell State ⓘ
mTOR↓, 1, p‑mTOR↓, 1, PI3K↓, 1, PTEN↑, 1, TumCG↓, 1,
Migration ⓘ
TumCI↓, 1, TumCMig↓, 2, TumCP↓, 2, TumMeta↓, 1,
Angiogenesis & Vasculature ⓘ
angioG↓, 1,
Barriers & Transport ⓘ
AQPs↓, 4,
Immune & Inflammatory Signaling ⓘ
Inflam↓, 1,
Cellular Microenvironment ⓘ
NOX↓, 1,
Drug Metabolism & Resistance ⓘ
eff↝, 1, selectivity↑, 1,
Functional Outcomes ⓘ
AntiCan↑, 1, cardioP↑, 1, chemoPv↑, 1, neuroP↑, 1,
Total Targets: 27
Pathway results for Effect on Normal Cells:
Proliferation, Differentiation & Cell State ⓘ
HDAC3↓, 1,
Barriers & Transport ⓘ
AQPs↓, 3,
Protein Aggregation ⓘ
Aβ↓, 1,
Functional Outcomes ⓘ
cognitive↑, 1,
Total Targets: 4
Scientific Paper Hit Count for: AQPs, Aquaporins
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#:1324 State#:% Dir#:1
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