Protein-Protein Interaction Network Analysis and Identification of Key Players in nor-NOHA and NOHA Mediated Pathways for Treatment of Cancer through Arginase Inhibition: Insights from Systems Biology
Abstract
L-arginine is involved in a number of biological processes in our bodies. Metabolism of L-arginine by the enzyme arginase has been found to be associated with cancer cell proliferation. Arginase inhibition has been proposed as a potential therapeutic means to inhibit this process. N-hydroxy-nor-L-Arg (nor-NOHA) and N (omega)-hydroxy-L-arginine (NOHA) has shown promise in inhibiting cancer progression through arginase inhibition. In this study, nor-NOHA and NOHA-associated genes and proteins were analyzed with several Bioinformatics and Systems Biology tools to identify the associated pathways and the key players involved so that a more comprehensive view of the molecular mechanisms including the regulatory mechanisms can be achieved and more potential targets for treatment of cancer can be discovered. Based on the analyses carried out, 3 significant modules have been identified from the PPI network. Five pathways/processes have been found to be significantly associated with nor-NOHA and NOHA associated genes. Out of the 1996 proteins in the PPI network, 4 have been identified as hub proteins-SOD, SOD1, AMD1, and NOS2. These 4 proteins have been implicated in cancer by other studies. Thus, this study provided further validation into the claim of these 4 proteins being potential targets for cancer treatment.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Elevated arginine levels in liver tumors promote metabolic reprogramming and tumor growth
D. Mossmann, S. Park, … M. N. Hall·bioRxiv·Apr 26, 2022
- Identification of druggable targets from the interactome of the Androgen Receptor and Serum Response Factor pathways in prostate cancer.
Haleema Azam, Colin Veale, … Maria Prencipe·PLoS ONEPeer-reviewed·Dec 13, 2024
- Systems level profiling of arginine starvation reveals MYC and ERK adaptive metabolic reprogramming
C. B. Brashears, R. Rathore, … J. M. Held·bioRxiv·Jan 13, 2020
- Independence of HIF1a and androgen signaling pathways in prostate cancer
M. G. Tran, B. A. Bibby, … D. Neal·bioRxiv·Nov 26, 2019
- Androgen receptor signaling blockade enhances NK cell-mediated killing of prostate cancer cells and sensitivity to NK cell checkpoint blockade
M. Pinho-Schwermann, C. Purcell, … W. S. El-Deiry·bioRxiv·Nov 15, 2023
- Loss of Arginase 2 Promotes Lung Metastasis in immune-competent hosts via Nitric Oxide Synthase 2-Dependent Th17 Response
Shu-Ting Chou, Xiaoyong Wang, … Jin Chen·bioRxiv·Jun 8, 2026