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Image Search Results
Journal: Journal of theoretical biology
Article Title: Dynamic modeling of signal transduction by mTOR complexes in cancer.
doi: 10.1016/j.jtbi.2019.109992
Figure Lengend Snippet: Fig. 1. mTOR complex organization and functions. mTOR plays its role in signal integration through two distinct complexes (mTORC1 and mTORC2). Each of these compo- nents is responsible for transducing appropriate signals into distinct responses.
Article Snippet: Contents lists available at ScienceDirect Journal of Theoretical Biology journal homepage: www.elsevier.com/locate/jtb Dynamic modeling of signal transduction by mTOR complexes in cancer Mohammadreza Dorvash a , b , 1 , Mohammad Farahmandnia b , c , 1 , Pouria Mosaddeghi a , b , c , 1 , Mitra Farahmandnejad a , b , c , Hosein Saber a , c , Mohammadhossein Khorraminejad-Shirazi b , c , Amir Azadi a , d , Iman Tavassoly e , ∗ a Pharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran b Cell and Molecular Medicine Student Research Group, Faculty of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran c Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran d Department of Pharmaceutics, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran e Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, 1425 Madison Ave, New York, NY 10029, USA a r t i c l e i n f o Article history: Received 10 May 2019 Revised 5 August 2019 Accepted 2 September 2019 Available online 4 September 2019 Keywords:
Techniques:
Journal: Journal of theoretical biology
Article Title: Dynamic modeling of signal transduction by mTOR complexes in cancer.
doi: 10.1016/j.jtbi.2019.109992
Figure Lengend Snippet: Fig. 2. The schematic interaction diagram representing the mechanism of inhibition of mTOR by rapamycin. (Thicker arrows represent higher rate constant for that direction).
Article Snippet: Contents lists available at ScienceDirect Journal of Theoretical Biology journal homepage: www.elsevier.com/locate/jtb Dynamic modeling of signal transduction by mTOR complexes in cancer Mohammadreza Dorvash a , b , 1 , Mohammad Farahmandnia b , c , 1 , Pouria Mosaddeghi a , b , c , 1 , Mitra Farahmandnejad a , b , c , Hosein Saber a , c , Mohammadhossein Khorraminejad-Shirazi b , c , Amir Azadi a , d , Iman Tavassoly e , ∗ a Pharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran b Cell and Molecular Medicine Student Research Group, Faculty of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran c Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran d Department of Pharmaceutics, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran e Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, 1425 Madison Ave, New York, NY 10029, USA a r t i c l e i n f o Article history: Received 10 May 2019 Revised 5 August 2019 Accepted 2 September 2019 Available online 4 September 2019 Keywords:
Techniques: Inhibition
Journal: Journal of theoretical biology
Article Title: Dynamic modeling of signal transduction by mTOR complexes in cancer.
doi: 10.1016/j.jtbi.2019.109992
Figure Lengend Snippet: Fig. 3. Temporal concentration of rapamycin for regimens I–IV. Since the plasma protein binding of the rapamycin is set aside, the concentration of free Cytosolic rapamycin is equal to its total concentration. Each regimen is simulated while scanning the “amount ± 20%” area (linearly stepped) around the dose administered. (A) Regimen Ⅰ : 8.0 × 10 −20 ± 20% mole/Day; (B) Regimen Ⅱ : 5.6 × 10 −19 ± 20% mole/Day; (C) Regimen Ⅲ : 5.6 × 10 −19 ± 20% mole/Week; and (D) Regimen Ⅳ : 2.24 × 10 −18 ± 20% mole/ Week.
Article Snippet: Contents lists available at ScienceDirect Journal of Theoretical Biology journal homepage: www.elsevier.com/locate/jtb Dynamic modeling of signal transduction by mTOR complexes in cancer Mohammadreza Dorvash a , b , 1 , Mohammad Farahmandnia b , c , 1 , Pouria Mosaddeghi a , b , c , 1 , Mitra Farahmandnejad a , b , c , Hosein Saber a , c , Mohammadhossein Khorraminejad-Shirazi b , c , Amir Azadi a , d , Iman Tavassoly e , ∗ a Pharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran b Cell and Molecular Medicine Student Research Group, Faculty of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran c Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran d Department of Pharmaceutics, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran e Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, 1425 Madison Ave, New York, NY 10029, USA a r t i c l e i n f o Article history: Received 10 May 2019 Revised 5 August 2019 Accepted 2 September 2019 Available online 4 September 2019 Keywords:
Techniques: Concentration Assay, Clinical Proteomics, Protein Binding
Journal: Journal of theoretical biology
Article Title: Dynamic modeling of signal transduction by mTOR complexes in cancer.
doi: 10.1016/j.jtbi.2019.109992
Figure Lengend Snippet: Fig. 5. Temporal concentration of rapamycin, mTORC1, and mTORC2 for different absorption and elimination rate constants (macro-constants) of rapamycin: the K abs@Rapam and K el@Rapam were scanned jointly in an area within a percentage range logarithmically spaced from −2 logs to + 2 logs using three steps each, making nine possible combinations for these kinetic parameters. The reference dose used for this parameter scan is 5.0 × 10 −19 mole/Day (regimen Ⅱ ). The plot at the center is where the K abs@Rapam and K el@Rapam are at their initial values. (K abs@Rapam = absorption rate constant; K el@Rapam = elimination rate constant).
Article Snippet: Contents lists available at ScienceDirect Journal of Theoretical Biology journal homepage: www.elsevier.com/locate/jtb Dynamic modeling of signal transduction by mTOR complexes in cancer Mohammadreza Dorvash a , b , 1 , Mohammad Farahmandnia b , c , 1 , Pouria Mosaddeghi a , b , c , 1 , Mitra Farahmandnejad a , b , c , Hosein Saber a , c , Mohammadhossein Khorraminejad-Shirazi b , c , Amir Azadi a , d , Iman Tavassoly e , ∗ a Pharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran b Cell and Molecular Medicine Student Research Group, Faculty of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran c Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran d Department of Pharmaceutics, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran e Department of Pharmacological Sciences, Icahn School of Medicine at Mount Sinai, 1425 Madison Ave, New York, NY 10029, USA a r t i c l e i n f o Article history: Received 10 May 2019 Revised 5 August 2019 Accepted 2 September 2019 Available online 4 September 2019 Keywords:
Techniques: Concentration Assay