AI Article Synopsis

  • This study investigates the anticancer effects of arginine-reduced graphene (Gr-Arg) and its combination with ginsenoside Rh2 (Gr-Arg-Rh2) in a mouse model of breast cancer.
  • Thirty-two mice were divided into four treatment groups over 32 days, with assessments focusing on tumor characteristics and gene expression related to cancer.
  • Results indicated that Gr-Arg-Rh2 significantly reduced tumor growth and increased survival rates, showing no metastasis, while also affecting gene expression levels in a positive manner compared to controls.

Article Abstract

Objectives: This study aims to evaluate the anticancer activity of arginine-reduced graphene (Gr-Arg) and ginsenoside Rh2-containing arginine-reduced graphene (Gr-Arg-Rh2).

Materials And Methods: Thirty-two mice with breast cancer were divided into four groups and treated every three days for 32 days: Group 1, PBS, Group 2, Rh2, Group 3, Gr-Arg, and Group 4, Gr-Arg-Rh2. The tumor size and weight, gene expression (IL10, INF-γ, TGFβ, and FOXP3), and pathological properties of the tumor and normal tissues were assessed.

Results: Results showed a significant decrease in expression for all drug treatment groups compared with the controls (=0.04). There was no significant difference among the groups regarding and gene expression profiles (>0.05). Gr-Arg-Rh2 significantly inhibited tumor growth (size and weight) compared with Rh2 and control groups. The highest survival rate and the highest percentage of tumor necrosis (87.5%) belonged to the Gr-Arg-Rh2 group. Lungs showed metastasis in the control group. No metastasis was observed in the Gr-Arg-Rh2 group. Gr-Arg-Rh2 showed partial degeneration of hepatocytes and acute cell infiltration in the portal spaces and around the central vein. The Gr-Arg group experienced a moderate infiltration of acute cells into the port spaces and around the central vein. The Rh2 group also showed a mild infiltration of acute and chronic cells in portal spaces.

Conclusion: Based on the results, Gr-Arg-Rh2 can reduce tumor size, weight, and growth, TGF-β gene expression, and increase tumor necrosis and survival time in mice with cancer.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742569PMC
http://dx.doi.org/10.22038/IJBMS.2022.66065.14524DOI Listing

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Article Synopsis
  • This study investigates the anticancer effects of arginine-reduced graphene (Gr-Arg) and its combination with ginsenoside Rh2 (Gr-Arg-Rh2) in a mouse model of breast cancer.
  • Thirty-two mice were divided into four treatment groups over 32 days, with assessments focusing on tumor characteristics and gene expression related to cancer.
  • Results indicated that Gr-Arg-Rh2 significantly reduced tumor growth and increased survival rates, showing no metastasis, while also affecting gene expression levels in a positive manner compared to controls.
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Ultra-sensitive electrochemical detection of oxidative stress biomarker 8-hydroxy-2'-deoxyguanosine with poly (L-arginine)/graphene wrapped Au nanoparticles modified electrode.

Biosens Bioelectron

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College of Chemistry and Chemical Engineering, Henan University, China; Key Laboratory of Natural Medicine and Immune-Engineering of Henan Province, Kaifeng 475004, Henan, China. Electronic address:

An innovative electrochemical sensor assembly relying on a simple "green" electrochemical reduction route is presented for the sensitive detection of 8-hydroxy-2'-deoxyguanosine (8-OHdG), the most abundant oxidative product of DNA. The sensing film consisted of poly (L-arginine) and graphene wrapped Au nanoparticles was fabricated on glassy carbon electrode (GCE/P-Arg/ErGO-AuNPs) using subsequent 'layer-by-layer' regime through electrochemical technique. The proposed method was also successfully applied for the quantification of 8-OHdG in the presence of interfering biomolecules like ascorbic acid and uric acid.

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