ER(estro) Cancer Research Results
ER(estro), Estrogen receptor: Click to Expand ⟱
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Estrogen receptor (ER) signaling is a critical regulator of cell proliferation, differentiation, and survival in breast cancer (BC) and other hormone-sensitive cancers.
Estrogen receptors, including ERα and ERβ, are often expressed, but the prognosis with the expression varies.
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Scientific Papers found: Click to Expand⟱
*Inflam↓, hydrogen inhalation exhibit anti-inflammatory and anti-oxidant effects in many studies.
*antiOx↑,
*NLRP3↓, decline of nucleotide-binding domain leucin-rich repeat and pyrin domain-containing protein 3 (NLRP3) was proved to inhibit memory impairment and Aβ deposition.4
*memory↑,
*Aβ↓,
*AMPK↑, hydrogen-rich water can stimulate AMPK-Sirt1-FoxO3a pathway
*SIRT1↑,
*FOXO3↑,
*p‑p38↓, hydrogen water could suppress the activation of phospho-p38 and JNK
*JNK↓,
*ROS↓, hydrogen can reduce neuronal apoptosis by inhibiting ROS-activated caspase signaling and protecting mitochondria.
*cognitive↑, Currently, Hou et al.50 reported that hydrogen-rich water could improve cognition function in female transgenic AD mice by reducing the decline in brain estrogen levels, estrogen receptor (ER) β
*ER(estro)↑,
*BDNF↑, and the expression of brain-derived neurotrophic factor (BDNF),
*ROS↓, MSM treatment improved histopathological insults and ameliorated level of oxidative stress, neuroinflammation and AD markers as well as modulated TREM-2/DAP-12/Syk pathway.
*Inflam↓,
*neuroP↑, The crucial role of MSM in the exerted neuroprotection is elicited via enhancing estrogen receptors signaling (ERα and ERβ), restoring Nrf-2/HO-1 signaling and promoting redoxins (Trx-1 and Grx-1)
*ER(estro)↑,
*NRF2↑,
*HO-1↑,
*Trx1↑,
*TXNIP↓, along with inhibiting TXNIP, reducing oxidative stress (MDA and NOx) and up-regulating anti-
oxidant machinery (GSH, GPx, SOD and CAT), d
*MDA↓,
*NOX↓,
*GSH↑,
*GPx↑,
*SOD↑,
*Catalase↑,
*BDNF↑, retrieving BDNF level and suppressing AchE activity, reducing tau-phosphorylation and curbing NFTs formation, decreasing AB production.
*AChE↓,
*p‑tau↓,
*Aβ↓,
*antiOx↑, Quercetin is considered to be a strong antioxidant due to its ability to scavenge free radicals
and bind transition metal ions. T
*lipid-P↓, properties of quercetin allow it to inhibit lipid peroxidation
*TNF-α↓, Quercetin significantly inhibited TNF-α production and gene expression in a dose-dependent
manner
*NF-kB↓, inhibiting the activation of NF-κβ,
*COX2↓, Quercetin also inhibits the enzymes cyclooxygenase
*IronCh↑, Quercetin also chelates ions of transition metals such as iron which can initiate the formation of oxygen free radicals
P53↓, Quercetin (248 microM) was found to down regulate expression of mutant p53 protein to
nearly undetectable levels in human breast cancer cell lines.
TumCCA↑, Quercetin has been found to arrest human leukemic T-cells in the late G1 phase
of the cell cycle.
HSPs↓, Quercetin has been found to inhibit production of heat shock proteins in several malignant
cell lines, including breast cancer,[52] leukemia,[53] and colon cancer.[
P21↓, Quercetin (10 microM) has been found to inhibit the expression of the p21-ras oncogene in
cultured colon cancer cell lines
RAS↓,
ER(estro)↑, Quercetin has been shown to induce ER II expression in both type I estrogen receptor positive (ER+) and type I estrogen
receptor negative (ER-) human breast cancer cells
OS?, Animals treated daily with 40 mg/kg quercetin had a 20-percent increase in life span, while those treated with 160 mg/kg rutin had a 50% increase in
life span.
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:
Protein Folding & ER Stress ⓘ
HSPs↓, 1,
DNA Damage & Repair ⓘ
P53↓, 1,
Cell Cycle & Senescence ⓘ
P21↓, 1, TumCCA↑, 1,
Proliferation, Differentiation & Cell State ⓘ
RAS↓, 1,
Hormonal & Nuclear Receptors ⓘ
ER(estro)↑, 1,
Functional Outcomes ⓘ
OS?, 1,
Total Targets: 7
Pathway results for Effect on Normal Cells:
Redox & Oxidative Stress ⓘ
antiOx↑, 2, Catalase↑, 1, GPx↑, 1, GSH↑, 1, HO-1↑, 1, lipid-P↓, 1, MDA↓, 1, NRF2↑, 1, ROS↓, 2, SOD↑, 1, Trx1↑, 1,
Metal & Cofactor Biology ⓘ
IronCh↑, 1,
Core Metabolism/Glycolysis ⓘ
AMPK↑, 1, SIRT1↑, 1,
Cell Death ⓘ
JNK↓, 1, p‑p38↓, 1,
Proliferation, Differentiation & Cell State ⓘ
FOXO3↑, 1,
Migration ⓘ
TXNIP↓, 1,
Immune & Inflammatory Signaling ⓘ
COX2↓, 1, Inflam↓, 2, NF-kB↓, 1, TNF-α↓, 1,
Cellular Microenvironment ⓘ
NOX↓, 1,
Synaptic & Neurotransmission ⓘ
AChE↓, 1, BDNF↑, 2, p‑tau↓, 1,
Protein Aggregation ⓘ
Aβ↓, 2, NLRP3↓, 1,
Hormonal & Nuclear Receptors ⓘ
ER(estro)↑, 2,
Functional Outcomes ⓘ
cognitive↑, 1, memory↑, 1, neuroP↑, 1,
Total Targets: 32
Scientific Paper Hit Count for: ER(estro), Estrogen receptor
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#:360 State#:% Dir#:2
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