Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
| Cat.No. | Product Name | Price |
|---|---|---|
| CSC-DC010581 | Panoply™ Human NQO1 Knockdown Stable Cell Line | Inquiry |
| CSC-SC010581 | Panoply™ Human NQO1 Over-expressing Stable Cell Line | Inquiry |
| Cat.No. | Product Name | Price |
|---|---|---|
| AD10971Z | Human NQO1 adenoviral particles | Inquiry |
| LV19830L | human NQO1 (NM_000903) lentivirus particles | Inquiry |
| LV19831L | human NQO1 (NM_001025433) lentivirus particles | Inquiry |
| LV19832L | human NQO1 (NM_001025434) lentivirus particles | Inquiry |
| Cat.No. | Product Name | Price |
|---|---|---|
| SHR019614 | shRNA set against Mouse Nqo1(NM_008706.5) | Inquiry |
| SHH354588 | shRNA set against Human NQO1 (NM_000903.2) | Inquiry |
| SHH354592 | shRNA set against Mouse NQO1 (NM_008706.5) | Inquiry |
| SHH354596 | shRNA set against Rat NQO1 (NM_017000.3) | Inquiry |
| SHR019478 | shRNA set against Human NQO1(NM_001025433.1) | Inquiry |
| SHR019496 | shRNA set against Rat Nqo1(NM_017000.3) | Inquiry |
| SHR019532 | shRNA set against Human NQO1(NM_001025434.1) | Inquiry |
| SHR019550 | shRNA set against Human NQO1(NM_000903.2) | Inquiry |
| SHW003941 | shRNA set against Chicken NQO1 (NM_001277619) | Inquiry |
| SHW003942 | shRNA set against Chicken NQO1 (NM_001277620) | Inquiry |
| SHW003943 | shRNA set against Chicken NQO1 (NM_001277621) | Inquiry |
| SHW013901 | shRNA set against Danio rerio NQO1 (NM_001204272) | Inquiry |
| SHW017476 | shRNA set against Danio rerio NQO1 (NM_205542) | Inquiry |
| Cat.No. | Product Name | Price |
|---|---|---|
| MiUTR1M-07796 | NQO1 miRNA 3'UTR clone | Inquiry |
| MiUTR1H-06889 | NQO1 miRNA 3'UTR clone | Inquiry |
| MiUTR1H-06888 | NQO1 miRNA 3'UTR clone | Inquiry |
| CDFR011070 | Rat Nqo1 cDNA Clone(NM_017000.3) | Inquiry |
| CDFH012756 | Human NQO1 cDNA Clone(NM_001025433.1) | Inquiry |
| CDFH012755 | Human NQO1 cDNA Clone(NM_001025434.1) | Inquiry |
| CDFH012754 | Human NQO1 cDNA Clone(NM_000903.2) | Inquiry |
| MiUTR1H-06890 | NQO1 miRNA 3'UTR clone | Inquiry |
| CDCR378113 | Rat Nqo1 ORF Clone(NM_017000.3) | Inquiry |
| CDCR245990 | Mouse Nqo1 ORF Clone(NM_008706.5) | Inquiry |
| CDCL139607 | Mouse NQO1 ORF clone (NM_001025434.1) | Inquiry |
| CDCL139605 | Mouse NQO1 ORF clone (NM_001025433.1) | Inquiry |
| CDCB191495 | Rabbit NQO1 ORF clone (XM_002711667.2) | Inquiry |
| CDCB178951 | Danio rerio NQO1 ORF Clone (NM_205542) | Inquiry |
| CDCB175376 | Danio rerio NQO1 ORF Clone (NM_001204272) | Inquiry |
| CDCB165418 | Chicken NQO1 ORF Clone (NM_001277621) | Inquiry |
| CDCB165417 | Chicken NQO1 ORF Clone (NM_001277620) | Inquiry |
| CDCL185516 | Human NQO1 ORF clone(NM_000903.2) | Inquiry |
| CDCB165416 | Chicken NQO1 ORF Clone (NM_001277619) | Inquiry |
NAD(P)H: Qinionoxedoreducase1 (NQO1), also known as DT-lipoamide dehydrogenase (DT- diaphorase), is a flavin protease containing 274 amino acids. It is expressed in various tissues and organs of mammals, is abnormally expressed in various cancer tissues, and plays an important role in the metabolic detoxification of benzene. NQO1 is an inducible reductase. Various chemical factors such as polycyclic aromatic hydrocarbons, hydroquinones, acrylates, phenolic antioxidants and azo dyes, and environmental factors such as hypoxia can induce their growth.
Functions of NQO1
The chemical protection of NQO1 is closely related to the metabolism of quinone compounds. As a toxic compound, quinone can induce canceration and necrosis of mammalian cells. It exists widely in nature, such as automobile exhaust, tobacco smoke, and even many foods and vitamins (VE, VK, tocopherol). NQO1 can catalyze the conversion of quinone groups to hydroquinone, avoiding nucleophilic damage DNA, reducing the damage to these organelles and genetic material caused by these oxidative active substances, and ensuring the normal physiological function of the body.
NQO1 has been shown to be able to stabilize the expression of wild-type p53 protein and inhibit its degradation through direct protein-protein interactions. Especially when the cells are out of oxidative stress, this stabilizing effect on p53 protein is more prominent. This causes the damaged cells to stop growing in time, undergo repair or undergo apoptosis, block the cell mutation process, and exert their anti-tumor effects. Another study showed that p53 lacks functional NQO1 in cells below the basic level.
Figure 1. Schematic summarization of NAD(P)H-quinone oxidoreductase 1 (NQO1) functions. (Pimradasiri Srijiwangsa., et al. 2016)
NQO1 and Cancer Treatment
NQO1 is a key enzyme for the body to protect against active oxygen species and suppress tumors. It can convert estrogen benzoquinone to catechol estrogen, thus limiting the level of estrogen benzoquinone that affects DNA and preventing DNA damage. In estrogen-induced breast cancer, the oxidative stress response produced by the redox cycle between catechol estrogen and estrogen benzoquinone plays an important role. NQO1 not only prevents the estrogen benzoquinone from acting on DNA, but also antagonizes the estrogen-induced oxidative stress response and thus inhibits estrogen-mediated DNA oxidative damage.
Shikonin is a potent inhibitor of the estrogen activation signal in breast cancer cells, and lifetime use of shikonin may reduce the risk of tumor recurrence. In vitro experiments with MCF-7 cell lines confirmed that shikonin can inhibit the growth of estrogen-dependent MCF-7 metastases. Shikonin exerts its chemopreventive effect by activating the detoxifying enzyme NQO1. It activates NQO1 transcription through at least three mechanisms: consumption of ERα receptors; increase in the body's important cell defense mechanism transcription factor NRF2 gene transcription and N2O2 transcriptional activation.
Resveratrol (3,4',5-trihydroxystilbene) prevents malignant tumors by regulating tumor-related pathways, preventing cell proliferation and inducing apoptosis. It can treat and prevent breast cancer by blocking multiple ways of estrogen genotoxicity. Resveratrol induces NQO1 expression and intracellular redistribution, thereby exerting its chemopreventive effect on breast cancer. It can act on estrogen metabolism and the formation of estrogen-DNA adducts, protecting cells from the carcinogenic effects of estrogen metabolites. These studies indicate that inhibiting estrogen signal transduction and activating NQO1 may be a good strategy for preventing estrogen-dependent breast cancer.
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