CYP1B1 Cancer Research Results
CYP1B1, Cytochrome P450 Family 1 Subfamily B Member 1: Click to Expand ⟱
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CYP1B1 (Cytochrome P450 Family 1 Subfamily B Member 1) is a xenobiotic- and hormone-metabolizing enzyme involved in oxidative metabolism, particularly of estrogens and procarcinogens.
-overexpressed in cancer, with poor prognosis
-A striking feature of CYP1B1 is its consistent overexpression in many tumors with minimal expression in adjacent normal tissue.
CYP1B1 overactivity contributes to cancer by:
-Increasing DNA damage burden
-Promoting genomic instability
-Supporting hormone-driven proliferation
-Modulating local redox balance (Generates reactive oxygen species (ROS))
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Scientific Papers found: Click to Expand⟱
CYP1A1↓, CYP1A1 and CYP1B1 bactosomes on a fluorogenic assay, we first demonstrated that DTS moderately inhibited both enzymes with half maximal inhibitory concentration (IC50) values of 1.3 ± 0.3 and 1.7 ± 0.3 μM,
CYP1B1↓,
chemoPv↑, these results demonstrate that DTS is a direct, reversible, competitive inhibitor of the carcinogen-activating CYP1A enzyme, binding in the active site pocket close to the heme site, and shows potential in chemoprevention.
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in-vitro, |
BC, |
MDA-MB-231 |
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TumCP↓, We found that HNK significantly inhibited proliferation and induced apoptosis on BC cell lines in a dose-dependent manner.
Apoptosis↓,
TumCMig↓, HNK treatment suppressed migration and colony formation and initiated the intrinsic apoptotic pathway specifically in MDA-MB-231 cells.
CYP1B1↓, miR-148a-5p expression was significantly up-regulated, whereas CYP1B1 expression was down-regulated following HNK treatment.
ChemoSen↑, strong synergistic effect between HNK and paclitaxel was observed in vitro.
*CYP1A1↓, Estrogen-induced expression of CYP450 1B1 and CYP450 1A1 was attenuated by the hops extract.
*CYP1B1↓,
2/16-OHE1↑, shown that it induces CyP4501A1, increasing 2-hydroxylation of estrogens, leading to the protective 2-OHE1, and also decreases CyP1B1 sharply, inhibiting 4-hydroxylation of estradiol, thereby decreasing the formation of the carcinogenic 4-OHE1.
CYP1B1↓,
4-OHE1↓,
Apoptosis↑, indole-3-carbinol has been shown to have direct effects on apoptosis and cyclin D, resulting in blockage of the cell cycle.
cycD1/CCND1↓,
TumCCA↑,
AntiTum↑, In addition to its antitumor activity in animals, it has also been shown to be effective against HPV-mediated tumors in human patients
Showing Research Papers: 1 to 4 of 4
* indicates research on normal cells as opposed to diseased cells
Total Research Paper Matches: 4
Pathway results for Effect on Cancer / Diseased Cells:
NA, unassigned(tgid=0) ⓘ
2/16-OHE1↑, 1, 4-OHE1↓, 1,
Redox & Oxidative Stress(tgid=1) ⓘ
CYP1A1↓, 1,
Cell Death(tgid=5) ⓘ
Apoptosis↓, 1, Apoptosis↑, 1,
DNA Damage & Repair(tgid=10) ⓘ
CYP1B1↓, 3,
Cell Cycle & Senescence(tgid=11) ⓘ
cycD1/CCND1↓, 1, TumCCA↑, 1,
Migration(tgid=13) ⓘ
TumCMig↓, 1, TumCP↓, 1,
Drug Metabolism & Resistance(tgid=21) ⓘ
ChemoSen↑, 1,
Functional Outcomes(tgid=23) ⓘ
AntiTum↑, 1, chemoPv↑, 1,
Total Targets: 13
Pathway results for Effect on Normal Cells:
Redox & Oxidative Stress(tgid=1) ⓘ
CYP1A1↓, 1,
DNA Damage & Repair(tgid=10) ⓘ
CYP1B1↓, 1,
Total Targets: 2
Scientific Paper Hit Count for: CYP1B1, Cytochrome P450 Family 1 Subfamily B Member 1
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#:1345 State#:% Dir#:1
wNotes=on sortOrder:rid,rpid
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