GSS Cancer Research Results
GSS, Glutathione Synthetase: Click to Expand ⟱
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GSS (Glutathione Synthetase) is a key enzyme in the synthesis of glutathione (GSH), an essential intracellular antioxidant that protects cells from oxidative stress and contributes to detoxification processes.
-GSS catalyzes the second step in glutathione synthesis, converting γ-glutamylcysteine and glycine into glutathione.
-Elevated expression of GSS has been observed in certain tumors as cancer cells adapt to high ROS levels. This adaptation can help protect malignant cells from apoptosis and contribute to chemoresistance.
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Scientific Papers found: Click to Expand⟱
*mtDam↓, CAP ameliorated mitochondrial damage, facilitated the nuclear translocation of NRF2, thereby promoting the expression of downstream antioxidant response elements, HO-1, Trx, GSS and NQO1 in GES-1 cells.
*NRF2↑,
*HO-1↑,
*Trx↑,
*GSS↑,
*NQO1↑,
*Keap1↓, CAP could directly bind to KEAP1 and inhibit the interaction between KEAP1 and NRF2.
*ROS↓, Capsaicin protects GES-1 from oxidative stress
*PKM2↓, Previous studies have demonstrated that CAP can directly bind to and inhibit the activity of PKM2 and LDHA, subsequently attenuating inflammatory response
*LDHA↓,
*Inflam↓,
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in-vitro, |
Colon, |
HT29 |
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in-vitro, |
CRC, |
SNU-407 |
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in-vitro, |
Nor, |
FHC |
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DNMTs↓, luteolin inhibited the expression of DNA methyltransferases, a transcription repressor, and increased the expression and activity of ten-eleven translocation (TET) DNA demethylases,
TET1↑,
NRF2↑, luteolin decreased the methylation of the Nrf2 promoter region, which corresponded to the increased mRNA expression of Nrf2
HDAC↓, Recently, Zao et al. demonstrated that luteolin epigenetically activates the Nrf2 pathway by downregulating DNA methyltransferase (DNMT) and histone deacetylase (HDAC) expression
tumCV↓, Luteolin decreased the viability of all three cell lines in a dose-dependent manner
BAX↑, luteolin upregulated the expression of the apoptotic protein Bax, active caspase-9, and active caspase-3, while it downregulated the expression of the anti-apoptotic protein Bcl-2,
Casp9↑,
Casp3↑,
Bcl-2↓,
ROS↓, Luteolin promotes ROS scavenging by inducing the expression of antioxidant enzymes
GSS↑, luteolin increased the protein expression of the antioxidant enzymes GCLc, GSS, catalase, and HO-1 in a dose- and time-dependent manner
Catalase↑,
HO-1↑,
DNMT1↓, Luteolin markedly decreased the protein expression of DNMT1, DNMT3A, and DNMT3B in a dose- and time-dependent manner
DNMT3A↓,
TET1↑, In contrast, it markedly increased the protein expression of TET1, TET2, and TET3 in a dose- and time-dependent manner
TET3↑,
TET2↓,
P53↑, Luteolin upregulated the expression of p53 and its target p21 in a dose- and time-dependent manner
P21↑,
*antiOx↑, antioxidant capabilities of shikonin and its ability to protect human keratinocytes from oxidative stress induced by fine particulate matter
*ROS↓, 3 µM was nontoxic to human keratinocytes and effectively scavenged reactive oxygen species (ROS) while increasing the production of reduced glutathione (GSH).
*GSH↑,
*GCLC↑, Shikonin increased the expression of GCLC and GSS via AKT and NRF2 activation
*GSS↑,
*Akt↑,
*NRF2↑,
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:
Redox & Oxidative Stress ⓘ
Catalase↑, 1, GSS↑, 1, HO-1↑, 1, NRF2↑, 1, ROS↓, 1,
Cell Death ⓘ
BAX↑, 1, Bcl-2↓, 1, Casp3↑, 1, Casp9↑, 1,
Transcription & Epigenetics ⓘ
TET3↑, 1, tumCV↓, 1,
DNA Damage & Repair ⓘ
DNMT1↓, 1, DNMT3A↓, 1, DNMTs↓, 1, P53↑, 1,
Cell Cycle & Senescence ⓘ
P21↑, 1,
Proliferation, Differentiation & Cell State ⓘ
HDAC↓, 1,
Migration ⓘ
TET1↑, 2,
Drug Metabolism & Resistance ⓘ
TET2↓, 1,
Total Targets: 19
Pathway results for Effect on Normal Cells:
Redox & Oxidative Stress ⓘ
antiOx↑, 1, GCLC↑, 1, GSH↑, 1, GSS↑, 2, HO-1↑, 1, Keap1↓, 1, NQO1↑, 1, NRF2↑, 2, ROS↓, 2, Trx↑, 1,
Mitochondria & Bioenergetics ⓘ
mtDam↓, 1,
Core Metabolism/Glycolysis ⓘ
LDHA↓, 1, PKM2↓, 1,
Cell Death ⓘ
Akt↑, 1,
Immune & Inflammatory Signaling ⓘ
Inflam↓, 1,
Total Targets: 15
Scientific Paper Hit Count for: GSS, Glutathione Synthetase
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#:1271 State#:% Dir#:2
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