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  1. Article ; Online: Efficacy of Providing the PI3K p110α Inhibitor BYL719 (Alpelisib) to Middle-Aged Mice in Their Diet.

    Hedges, Christopher P / Boix, Jordi / Jaiswal, Jagdish K / Shetty, Bhoopika / Shepherd, Peter R / Merry, Troy L

    Biomolecules

    2021  Volume 11, Issue 2

    Abstract: BYL719 (alpelisib) is a small molecule inhibitor of PI3K p110α developed for cancer therapy. Targeted suppression of PI3K has led to lifespan extension in rodents and model organisms. If PI3K inhibitors are to be considered as an aging therapeutic, it is ...

    Abstract BYL719 (alpelisib) is a small molecule inhibitor of PI3K p110α developed for cancer therapy. Targeted suppression of PI3K has led to lifespan extension in rodents and model organisms. If PI3K inhibitors are to be considered as an aging therapeutic, it is important to understand the potential consequences of long-term exposure, and the most practical way to achieve this is through diet administration. Here, we investigated the pharmacokinetics of BYL719 delivered in diet and the efficacy of BYL719 to suppress insulin signaling when administered in the diet of 8-month-old male and female mice. Compared to oral gavage, diet incorporation resulted in a lower peak plasma BYL719 (3.6 vs. 9.2 μM) concentration but similar half-life (~1.5 h). Consuming BYL719 resulted in decreased insulin signaling in liver and muscle within 72 h, and mice still showed impaired glucose tolerance and insulin sensitivity following 6 weeks of access to a diet containing 0.3 g/kg BYL719. However, consuming BYL719 did not affect food intake, body mass, muscle function (rotarod and hang time performance) or cognitive behaviors. This provides evidence that BYL719 has long-term efficacy without major toxicity or side effects, and suggests that administering BYL719 in diet is suitable for studying the effect of pharmacological suppression of PI3K p110α on aging and metabolic function.
    MeSH term(s) Aging ; Animals ; Behavior, Animal ; Class I Phosphatidylinositol 3-Kinases/genetics ; Female ; Glucose/metabolism ; Glucose Tolerance Test ; Homeostasis ; Liver/metabolism ; Male ; Mice ; Mice, Inbred C57BL ; Muscle, Skeletal/metabolism ; Muscles/metabolism ; Phosphatidylinositol 3-Kinases/metabolism ; Receptor, Insulin/metabolism ; Thiazoles/pharmacology
    Chemical Substances Thiazoles ; Alpelisib (08W5N2C97Q) ; 1-phosphatidylinositol 3-kinase p110 subunit, mouse (EC 2.7.1.137) ; Class I Phosphatidylinositol 3-Kinases (EC 2.7.1.137) ; Receptor, Insulin (EC 2.7.10.1) ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2021-01-25
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2701262-1
    ISSN 2218-273X ; 2218-273X
    ISSN (online) 2218-273X
    ISSN 2218-273X
    DOI 10.3390/biom11020150
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: In situ gelling system for sustained intraarticular delivery of bupivacaine and ketorolac in sheep.

    Abdeltawab, Hani / Bolam, Scott M / Jaiswal, Jagdish K / McGlashan, Sue R / Young, Simon W / Hill, Andrew / Svirskis, Darren / Sharma, Manisha

    European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V

    2022  Volume 174, Page(s) 35–46

    Abstract: Suboptimal control of postoperative pain following knee arthroplasty can slow recovery and reduce patient satisfaction. Intraarticular (IA) administration of bupivacaine and ketorolac offers efficient pain control and minimizes opioid consumption. ... ...

    Abstract Suboptimal control of postoperative pain following knee arthroplasty can slow recovery and reduce patient satisfaction. Intraarticular (IA) administration of bupivacaine and ketorolac offers efficient pain control and minimizes opioid consumption. However, the clinical benefits of this approach are short lived due to rapid clearance of drugs from the joint cavity. Here, we describe a poloxamer based thermoresponsive in situ gelling system for the sustained IA delivery of bupivacaine hydrochloride (BH) and ketorolac tromethamine (KT) following knee surgery in an ovine model. Drug loaded formulations were prepared using poloxamer 407, poloxamer 188 and sodium chloride. In vitro characterization was conducted, followed by in vivo evaluation of sustained drug release and safety in an ovine model of knee joint surgery. Rheological studies revealed a Newtonian-like flow of the developed formulation at room temperature, confirming its injectability, followed by a transition to a viscous gel as temperature approached body temperature. The developed formulation successfully sustained the in vivo release of BH for 72 h and KT for 48 h, as determined by circulating drug levels, compared to 24 and 8 h for marketed drug solutions. The concentrations of BH and KT in the synovial fluids at 72 h were 11.5 and 1.8 times that of marketed products, suggesting a significant increase in the IA residence time. The developed formulation induced a comparable inflammatory response compared to the marketed drug solutions, however a significantly higher chondrotoxicity was observed following administration of the gel formulations. Poloxamers based in situ gelling systems are promising delivery platforms for the sustained and localised IA delivery of BH and KT, with potential clinical benefits in managing the postoperative pain following knee arthroplasty.
    MeSH term(s) Animals ; Bupivacaine ; Gels ; Ketorolac ; Ketorolac Tromethamine ; Pain, Postoperative/drug therapy ; Poloxamer ; Sheep
    Chemical Substances Gels ; Poloxamer (106392-12-5) ; Ketorolac Tromethamine (4EVE5946BQ) ; Bupivacaine (Y8335394RO) ; Ketorolac (YZI5105V0L)
    Language English
    Publishing date 2022-03-29
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 1065368-5
    ISSN 1873-3441 ; 0939-6411
    ISSN (online) 1873-3441
    ISSN 0939-6411
    DOI 10.1016/j.ejpb.2022.03.012
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Nanoparticle-loaded biodegradable light-responsive in situ forming injectable implants for effective peptide delivery to the posterior segment of the eye.

    Bisht, Rohit / Jaiswal, Jagdish K / Rupenthal, Ilva D

    Medical hypotheses

    2017  Volume 103, Page(s) 5–9

    Abstract: Diseases affecting the posterior segment the eye, such as age-related macular degeneration (AMD), are the leading cause of blindness worldwide. Conventional dosage forms, such as eye drops, have to surmount several elimination mechanisms and complex ... ...

    Abstract Diseases affecting the posterior segment the eye, such as age-related macular degeneration (AMD), are the leading cause of blindness worldwide. Conventional dosage forms, such as eye drops, have to surmount several elimination mechanisms and complex barriers to achieve therapeutic concentrations at the target site often resulting in low anterior segment bioavailability (ca. 2-5%) with generally none of the drug reaching posterior segment tissues. Thus, frequent intravitreal injections are currently required to treat retinal conditions which have been associated with poor patient compliance due to pain, risk of infection, hemorrhages, retinal detachment and high treatment related costs. To partially overcome these issues, ocular implants have been developed for some posterior segment indications; however, the majority require surgical implantation and removal at the end of the intended treatment period. The transparent nature of the cornea and lens render light-responsive systems an attractive strategy for the management of diseases affecting the back of the eye. Light-responsive in situ forming injectable implants (ISFIs) offer various benefits such as ease of application in a minimally invasive manner and more site specific control over drug release. Moreover, the biodegradable nature of such implants avoids the need for surgical removal after release of the payload. Incorporating drug-loaded polymeric nanoparticles (NPs) into these implants may reduce the high initial burst release from the polymeric matrix and further sustain drug release thus avoiding the need for frequent injections as well as minimizing associated side effects. However, light-responsive systems for ophthalmic application are still in their early stages of development with limited reports on their safety and effectiveness. We hypothesize that the innovative design and properties of NP-containing light-responsive ISFIs can serve as a platform for effective management of ocular diseases requiring long term treatment.
    Language English
    Publishing date 2017-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 193145-3
    ISSN 1532-2777 ; 0306-9877
    ISSN (online) 1532-2777
    ISSN 0306-9877
    DOI 10.1016/j.mehy.2017.03.033
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Development of a novel stability indicating RP-HPLC method for quantification of Connexin43 mimetic peptide and determination of its degradation kinetics in biological fluids.

    Bisht, Rohit / Rupenthal, Ilva D / Sreebhavan, Sreevalsan / Jaiswal, Jagdish K

    Journal of pharmaceutical analysis

    2017  Volume 7, Issue 6, Page(s) 365–373

    Abstract: Connexin43 mimetic peptide (Cx43MP) has been intensively investigated for its therapeutic effect in the management of inflammatory eye conditions, spinal cord injury, wound healing and ischemia-induced brain damage. Here, we report on a validated ... ...

    Abstract Connexin43 mimetic peptide (Cx43MP) has been intensively investigated for its therapeutic effect in the management of inflammatory eye conditions, spinal cord injury, wound healing and ischemia-induced brain damage. Here, we report on a validated stability-indicating reversed-phase high performance liquid chromatography (RP-HPLC) method for the quantification of Cx43MP under stress conditions. These included exposure to acid/base, light, oxidation and high temperature. In addition, the degradation kinetics of the peptide were evaluated in bovine vitreous and drug-free human plasma at 37 °C. Detection of Cx43MP was carried out at 214 nm with a retention time of 7.5 min. The method showed excellent linearity over the concentration range of 0.9-250 µg/mL (
    Language English
    Publishing date 2017-06-23
    Publishing country China
    Document type Journal Article
    ZDB-ID 2630174-X
    ISSN 2095-1779
    ISSN 2095-1779
    DOI 10.1016/j.jpha.2017.06.008
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Nanocarrier mediated retinal drug delivery: overcoming ocular barriers to treat posterior eye diseases.

    Bisht, Rohit / Mandal, Abhirup / Jaiswal, Jagdish K / Rupenthal, Ilva D

    Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology

    2017  Volume 10, Issue 2

    Abstract: Effective drug delivery to the retina still remains a challenge due to ocular elimination mechanisms and complex barriers that selectively limit the entry of drugs into the eye. To overcome these barriers, frequent intravitreal injections are currently ... ...

    Abstract Effective drug delivery to the retina still remains a challenge due to ocular elimination mechanisms and complex barriers that selectively limit the entry of drugs into the eye. To overcome these barriers, frequent intravitreal injections are currently used to achieve high drug concentrations in vitreous and retina. However, these repetitive injections may result in several side effects. Recent advancements in the field of nanoparticle-based drug delivery could overcome some of these unmet needs and various preclinical studies conducted to date have demonstrated promising results of nanotherapies in the treatment of retinal diseases. Compared to the majority of commercially available ocular implants, the biodegradable nature of most nanoparticles (NPs) avoids the need for surgical implantation and removal after the release of the payload. In addition, the sustained drug release from NPs over an extended period of time reduces the need for frequent intravitreal injections and the risk of associated side effects. The nanometer size and highly modifiable surface properties make NPs excellent candidates for targeted ocular drug delivery. Studies have shown that nanocarriers enhance the intravitreal half-life and thus bioavailability of a number of drugs including proteins and peptides. In addition, they have shown promising results in delivering genetic material to the retinal tissues by protecting it from possible intravitreal degradation. This review covers the various challenges associated with drug delivery to the posterior segment of the eye, particularly the retina, and highlights the application of nanocarriers to overcome these challenges in context with recent advances in preclinical studies. WIREs Nanomed Nanobiotechnol 2018, 10:e1473. doi: 10.1002/wnan.1473 This article is categorized under: Therapeutic Approaches and Drug Discovery > Emerging Technologies Implantable Materials and Surgical Technologies > Nanomaterials and Implants.
    MeSH term(s) Delayed-Action Preparations/administration & dosage ; Delayed-Action Preparations/therapeutic use ; Drug Carriers/administration & dosage ; Drug Carriers/therapeutic use ; Humans ; Intravitreal Injections ; Nanomedicine ; Nanoparticles/administration & dosage ; Nanoparticles/therapeutic use ; Retinal Diseases/drug therapy
    Chemical Substances Delayed-Action Preparations ; Drug Carriers
    Language English
    Publishing date 2017-04-20
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2502698-7
    ISSN 1939-0041 ; 1939-5116
    ISSN (online) 1939-0041
    ISSN 1939-5116
    DOI 10.1002/wnan.1473
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Preclinical Activity and Pharmacokinetic/Pharmacodynamic Relationship for a Series of Novel Benzenesulfonamide Perforin Inhibitors.

    Gartlan, Kate H / Jaiswal, Jagdish K / Bull, Matthew R / Akhlaghi, Hedieh / Sutton, Vivien R / Alexander, Kylie A / Chang, Karshing / Hill, Geoffrey R / Miller, Christian K / O'Connor, Patrick D / Jose, Jiney / Trapani, Joseph A / Charman, Susan A / Spicer, Julie A / Jamieson, Stephen M F

    ACS pharmacology & translational science

    2022  Volume 5, Issue 6, Page(s) 429–439

    Abstract: Perforin is a key effector of lymphocyte-mediated cell death pathways and contributes to transplant rejection of immunologically mismatched grafts. We have developed a novel series of benzenesulfonamide (BZS) inhibitors of perforin that can mitigate ... ...

    Abstract Perforin is a key effector of lymphocyte-mediated cell death pathways and contributes to transplant rejection of immunologically mismatched grafts. We have developed a novel series of benzenesulfonamide (BZS) inhibitors of perforin that can mitigate graft rejection during allogeneic bone marrow/stem cell transplantation. Eight such perforin inhibitors were tested for their murine pharmacokinetics, plasma protein binding, and their ability to block perforin-mediated lysis
    Language English
    Publishing date 2022-05-31
    Publishing country United States
    Document type Journal Article
    ISSN 2575-9108
    ISSN (online) 2575-9108
    DOI 10.1021/acsptsci.2c00009
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: The CSF1 receptor inhibitor pexidartinib (PLX3397) reduces tissue macrophage levels without affecting glucose homeostasis in mice.

    Merry, Troy L / Brooks, Anna E S / Masson, Stewart W / Adams, Shannon E / Jaiswal, Jagdish K / Jamieson, Stephen M F / Shepherd, Peter R

    International journal of obesity (2005)

    2019  Volume 44, Issue 1, Page(s) 245–253

    Abstract: Background and objectives: Excessive adipose tissue macrophage accumulation in obesity has been implicated in mediating inflammatory responses that impair glucose homeostasis and promote insulin resistance. Colony-stimulating factor 1 (CSF1) controls ... ...

    Abstract Background and objectives: Excessive adipose tissue macrophage accumulation in obesity has been implicated in mediating inflammatory responses that impair glucose homeostasis and promote insulin resistance. Colony-stimulating factor 1 (CSF1) controls macrophage differentiation, and here we sought to determine the effect of a CSF1 receptor inhibitor, PLX3397, on adipose tissue macrophage levels and understand the impact on glucose homeostasis in mice.
    Methods: A Ten-week-old mice were fed a chow or high-fat diet for 10 weeks and then treated with PLX3397 via oral gavage (50 mg/kg) every second day for 3 weeks, with subsequent monitoring of glucose tolerance, insulin sensitivity and assessment of adipose tissue immune cells.
    Results: PLX3397 treatment substantially reduced macrophage numbers in adipose tissue of both chow and high-fat diet fed mice without affecting total myeloid cell levels. Despite this, PLX3397 did not greatly alter glucose homeostasis, did not affect high-fat diet-induced increases in visceral fat cytokine expression (Il-6 and Tnfa) and had limited effect on the phosphorylation of the stress kinases JNK and ERK and macrophage polarization.
    Conclusions: Our results indicate that macrophage infiltration of adipose tissue induced by a high-fat diet may not be the trigger for impairments in whole body glucose homeostasis, and that anti-CSF1 therapies are not likely to be useful as treatments for insulin resistance.
    MeSH term(s) Adipose Tissue/cytology ; Adipose Tissue/drug effects ; Aminopyridines/pharmacology ; Animals ; Diet, High-Fat ; Glucose/metabolism ; Homeostasis/drug effects ; Insulin Resistance/physiology ; Macrophages/drug effects ; Mice ; Obesity ; Pyrroles/pharmacology ; Receptors, Granulocyte-Macrophage Colony-Stimulating Factor/antagonists & inhibitors
    Chemical Substances Aminopyridines ; Csf1r protein, mouse ; Pyrroles ; Receptors, Granulocyte-Macrophage Colony-Stimulating Factor ; pexidartinib (6783M2LV5X) ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2019-03-29
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 752409-2
    ISSN 1476-5497 ; 0307-0565
    ISSN (online) 1476-5497
    ISSN 0307-0565
    DOI 10.1038/s41366-019-0355-7
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Schedule-dependent potentiation of chemotherapy drugs by the hypoxia-activated prodrug SN30000.

    Mao, Xinjian / McManaway, Sarah / Jaiswal, Jagdish K / Hong, Cho R / Wilson, William R / Hicks, Kevin O

    Cancer biology & therapy

    2019  Volume 20, Issue 9, Page(s) 1258–1269

    Abstract: Hypoxia-activated prodrugs (HAPs) are hypothesized to improve the therapeutic index of chemotherapy drugs that are ineffective against tumor cells in hypoxic microenvironments. SN30000 (CEN-209) is a benzotriazine di- ...

    Abstract Hypoxia-activated prodrugs (HAPs) are hypothesized to improve the therapeutic index of chemotherapy drugs that are ineffective against tumor cells in hypoxic microenvironments. SN30000 (CEN-209) is a benzotriazine di-
    MeSH term(s) Animals ; Antineoplastic Agents/pharmacology ; Cell Hypoxia ; Cell Line, Tumor ; Cyclic N-Oxides/pharmacology ; Disease Models, Animal ; Drug Synergism ; Humans ; Prodrugs/pharmacology ; Triazines/pharmacology ; Tumor Cells, Cultured ; Xenograft Model Antitumor Assays
    Chemical Substances Antineoplastic Agents ; CEN-209 ; Cyclic N-Oxides ; Prodrugs ; Triazines
    Language English
    Publishing date 2019-05-26
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2146305-0
    ISSN 1555-8576 ; 1538-4047
    ISSN (online) 1555-8576
    ISSN 1538-4047
    DOI 10.1080/15384047.2019.1617570
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Spatially-resolved pharmacokinetic/pharmacodynamic modelling of bystander effects of a nitrochloromethylbenzindoline hypoxia-activated prodrug.

    Hong, Cho Rong / Mehta, Sunali Y / Liyanage, H D Sarath / McManaway, Sarah P / Lee, Ho H / Jaiswal, Jagdish K / Bogle, Gib / Tercel, Moana / Pruijn, Frederik B / Wilson, William R / Hicks, Kevin O

    Cancer chemotherapy and pharmacology

    2021  Volume 88, Issue 4, Page(s) 673–687

    Abstract: Purpose: Hypoxia-activated prodrugs (HAPs) have the potential for eliminating chemo- and radiation-resistant hypoxic tumour cells, but their activity is often compromised by limited penetration into hypoxic zones. Nitrochloromethylbenzindoline (nitroCBI) ...

    Abstract Purpose: Hypoxia-activated prodrugs (HAPs) have the potential for eliminating chemo- and radiation-resistant hypoxic tumour cells, but their activity is often compromised by limited penetration into hypoxic zones. Nitrochloromethylbenzindoline (nitroCBI) HAPs are reduced in hypoxic cells to highly cytotoxic DNA minor groove alkylating aminoCBI metabolites. In this study, we investigate whether a lead nitroCBI, SN30548, generates a significant bystander effect through the diffusion of its aminoCBI metabolite and whether this compensates for any diffusion limitations of the prodrug in tumour tissue.
    Methods: Metabolism and uptake of the nitroCBI in oxic and anoxic cells, and diffusion through multicellular layer cultures, was characterised by LC-MS/MS. To quantify bystander effects, clonogenic cell killing of HCT116 cells was assessed in multicellular spheroid co-cultures comprising cells transfected with cytochrome P450 oxidoreductase (POR) or E. coli nitroreductase NfsA. Spatially-resolved pharmacokinetic/pharmacodynamic (PK/PD) models, parameterised by the above measurements, were developed for spheroids and tumours using agent-based and Green's function modelling, respectively.
    Results: NitroCBI was reduced to aminoCBI by POR under anoxia and by NfsA under oxia, and was the only significant cytotoxic metabolite in both cases. In spheroid co-cultures comprising 30% NfsA-expressing cells, non-metabolising cells were as sensitive as the NfsA cells, demonstrating a marked bystander effect. Agent-based PK/PD models provided good prediction of cytotoxicity in spheroids, while use of the same parameters in a Green's function model for a tumour microregion demonstrated that local diffusion of aminoCBI overcomes the penetration limitation of the prodrug.
    Conclusions: The nitroCBI HAP SN30548 generates a highly efficient bystander effect through local diffusion of its active metabolite in tumour tissue.
    MeSH term(s) Bystander Effect/drug effects ; Cell Hypoxia ; Chromatography, Liquid ; Coculture Techniques ; Escherichia coli Proteins/genetics ; HCT116 Cells ; Humans ; Indoles/pharmacokinetics ; Indoles/pharmacology ; Models, Biological ; NADPH-Ferrihemoprotein Reductase/genetics ; Nitroreductases/genetics ; Prodrugs ; Spheroids, Cellular/cytology ; Tandem Mass Spectrometry
    Chemical Substances Escherichia coli Proteins ; Indoles ; Prodrugs ; indoline (6DPT9AB2NK) ; NADPH-Ferrihemoprotein Reductase (EC 1.6.2.4) ; NfsA protein, E coli (EC 1.7.-) ; Nitroreductases (EC 1.7.-)
    Language English
    Publishing date 2021-07-10
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 6820-2
    ISSN 1432-0843 ; 0344-5704 ; 0943-9404
    ISSN (online) 1432-0843
    ISSN 0344-5704 ; 0943-9404
    DOI 10.1007/s00280-021-04320-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: An agent-based model for drug-radiation interactions in the tumour microenvironment: Hypoxia-activated prodrug SN30000 in multicellular tumour spheroids.

    Mao, Xinjian / McManaway, Sarah / Jaiswal, Jagdish K / Patel, Priyanka B / Wilson, William R / Hicks, Kevin O / Bogle, Gib

    PLoS computational biology

    2018  Volume 14, Issue 10, Page(s) e1006469

    Abstract: Multicellular tumour spheroids capture many characteristics of human tumour microenvironments, including hypoxia, and represent an experimentally tractable in vitro model for studying interactions between radiotherapy and anticancer drugs. However, ... ...

    Abstract Multicellular tumour spheroids capture many characteristics of human tumour microenvironments, including hypoxia, and represent an experimentally tractable in vitro model for studying interactions between radiotherapy and anticancer drugs. However, interpreting spheroid data is challenging because of limited ability to observe cell fate within spheroids dynamically. To overcome this limitation, we have developed a hybrid continuum/agent-based model (ABM) for HCT116 tumour spheroids, parameterised using experimental models (monolayers and multilayers) in which reaction and diffusion can be measured directly. In the ABM, cell fate is simulated as a function of local oxygen, glucose and drug concentrations, determined by solving diffusion equations and intracellular reactions. The model is lattice-based, with cells occupying discrete locations on a 3D grid embedded within a coarser grid that encompasses the culture medium; separate solvers are employed for each grid. The generated concentration fields account for depletion in the medium and specify concentration-time profiles within the spheroid. Cell growth and survival are determined by intracellular oxygen and glucose concentrations, the latter based on direct measurement of glucose diffusion/reaction (in multilayers) for the first time. The ABM reproduces known features of spheroids including overall growth rate, its oxygen and glucose dependence, peripheral cell proliferation, central hypoxia and necrosis. We extended the ABM to describe in detail the hypoxia-dependent interaction between ionising radiation and a hypoxia-activated prodrug (SN30000), again using experimentally determined parameters; the model accurately simulated clonogenic cell killing in spheroids, while inclusion of reversible cell cycle delay was required to account for the marked spheroid growth delay after combined radiation and SN30000. This ABM of spheroid growth and response exemplifies the utility of integrating computational and experimental tools for investigating radiation/drug interactions, and highlights the critical importance of understanding oxygen, glucose and drug concentration gradients in interpreting activity of therapeutic agents in spheroid models.
    MeSH term(s) Antineoplastic Agents/pharmacology ; Cell Hypoxia/physiology ; Cyclic N-Oxides/pharmacology ; HCT116 Cells ; Humans ; Models, Biological ; Prodrugs/pharmacology ; Radiotherapy ; Triazines/pharmacology ; Tumor Microenvironment/drug effects ; Tumor Microenvironment/radiation effects
    Chemical Substances Antineoplastic Agents ; CEN-209 ; Cyclic N-Oxides ; Prodrugs ; Triazines
    Language English
    Publishing date 2018-10-24
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2193340-6
    ISSN 1553-7358 ; 1553-734X
    ISSN (online) 1553-7358
    ISSN 1553-734X
    DOI 10.1371/journal.pcbi.1006469
    Database MEDical Literature Analysis and Retrieval System OnLINE

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