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34 pages, 11454 KiB  
Article
Compassionate Care with Autonomous AI Humanoid Robots in Future Healthcare Delivery: A Multisensory Simulation of Next-Generation Models
by Joannes Paulus Tolentino Hernandez
Biomimetics 2024, 9(11), 687; https://doi.org/10.3390/biomimetics9110687 - 11 Nov 2024
Viewed by 941
Abstract
The integration of AI and robotics in healthcare raises concerns, and additional issues regarding autonomous systems are anticipated. Effective communication is crucial for robots to be seen as “caring”, necessitating advanced mechatronic design and natural language processing (NLP). This paper examines the potential [...] Read more.
The integration of AI and robotics in healthcare raises concerns, and additional issues regarding autonomous systems are anticipated. Effective communication is crucial for robots to be seen as “caring”, necessitating advanced mechatronic design and natural language processing (NLP). This paper examines the potential of humanoid robots to autonomously replicate compassionate care. The study employs computational simulations using mathematical and agent-based modeling to analyze human–robot interactions (HRIs) surpassing Tetsuya Tanioka’s TRETON. It incorporates stochastic elements (through neuromorphic computing) and quantum-inspired concepts (through the lens of Martha Rogers’ theory), running simulations over 100 iterations to analyze complex behaviors. Multisensory simulations (visual and audio) demonstrate the significance of “dynamic communication”, (relational) “entanglement”, and (healthcare system and robot’s function) “superpositioning” in HRIs. Quantum and neuromorphic computing may enable humanoid robots to empathetically respond to human emotions, based on Jean Watson’s ten caritas processes for creating transpersonal states. Autonomous AI humanoid robots will redefine the norms of “caring”. Establishing “pluralistic agreements” through open discussions among stakeholders worldwide is necessary to align innovations with the values of compassionate care within a “posthumanist” framework, where the compassionate care provided by Level 4 robots meets human expectations. Achieving compassionate care with autonomous AI humanoid robots involves translating nursing, communication, computer science, and engineering concepts into robotic care representations while considering ethical discourses through collaborative efforts. Nurses should lead the design and implementation of AI and robots guided by “technological knowing” in Rozzano Locsin’s TCCN theory. Full article
(This article belongs to the Special Issue Optimal Design Approaches of Bioinspired Robots)
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Graphical abstract

Graphical abstract
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<p>Interpretation of Tanioka’s [<a href="#B10-biomimetics-09-00687" class="html-bibr">10</a>] model according to cybernetic HRI communication [<a href="#B92-biomimetics-09-00687" class="html-bibr">92</a>].</p>
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<p>Communication in “Level 3” HRI [<a href="#B92-biomimetics-09-00687" class="html-bibr">92</a>].</p>
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<p>Model validation for “Level 3” HRI [<a href="#B92-biomimetics-09-00687" class="html-bibr">92</a>].</p>
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<p>The representation of dissonance with “Level 3” HRI [<a href="#B92-biomimetics-09-00687" class="html-bibr">92</a>]. (Download the file at <a href="https://github.com/jphernandezrn/Data-Sonification-Human-Robot-Interaction" target="_blank">https://github.com/jphernandezrn/Data-Sonification-Human-Robot-Interaction</a> (accessed on 25 August 2024).</p>
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<p>The representation of Level 4 HRI. (Note: The mathematics in quantum communication is referenced from Yuan and Cheng [<a href="#B94-biomimetics-09-00687" class="html-bibr">94</a>], when discussing fidelity).</p>
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<p>The communication, entanglement, and superpositioning of the three states.</p>
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<p>Model validation involving overlapping states.</p>
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<p>The sonification of frequencies between states exhibiting quantum relationships. (Download the file at <a href="https://github.com/jphernandezrn/Data-Sonification-Human-Robot-Interaction" target="_blank">https://github.com/jphernandezrn/Data-Sonification-Human-Robot-Interaction</a>).</p>
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<p>An intuitive, self-regulating, and agile robot system architecture through steps 1–9. Note: <sup>a</sup> Information processing must be dynamic, symbolically instantiated (unsupervised), and evolving (unbounded materially) through <sup>c</sup> “state transition” (the humanoid robot’s conditions based on actions or events). Unbounded transitions refer to a system’s capacity for an unlimited number of transitions between states, often occurring when the conditions for transitions are not strictly defined or when the system can respond to a wide variety of inputs. In the real world, second-order cybernetics [<a href="#B99-biomimetics-09-00687" class="html-bibr">99</a>] should allow the operation of artificial cognition that is fluid and capable of co-creating knowledge within the healthcare network. <sup>b</sup> Alternatively, it can involve the construction and decomposition of “information granules” (the chunks of information) [<a href="#B95-biomimetics-09-00687" class="html-bibr">95</a>], applicable to both algorithmic (deductive) and non-algorithmic (inductive and abductive) computing using quantum logic. This process evolves through machine learning with quantum logic.</p>
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<p>Care actions and intentionality construed from wave function collapse.</p>
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<p>Model validation using machine learning.</p>
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<p>The data sonification of simulated care actions. Download the file at <a href="https://github.com/jphernandezrn/Data-Sonification-Human-Robot-Interaction" target="_blank">https://github.com/jphernandezrn/Data-Sonification-Human-Robot-Interaction</a> (accessed on 25 August 2024).</p>
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<p>The spectrogram comparison of the three audio files.</p>
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<p>The mathematical model simulation of “stochasticity” and “intentionality” in the humanoid robot. Note: The blue line represents the relationship between “stochasticity” and “intentionality” in a neuromorphic circuit, as modeled by the equation <span class="html-italic">I</span> = 0.5278 + 0.0666<span class="html-italic">S</span> − 0.0565<span class="html-italic">S</span><sup>2</sup>.) The pattern exhibits three distinct phases: Initial Rise (0.0 to ~0.45); Peak Plateau (~0.45 to ~0.8); and Final Decline (~0.8 to 1.0).</p>
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<p>The mathematical model simulation of adaptive learning in the humanoid robot. Note: The blue line (“Initial”) shows the robot’s behavior before learning, characterized by jagged fluctuations due to varying levels of randomness (stochasticity). In contrast, the red line (“After Learning”) presents a smoother curve with less variability, indicating enhanced stability after learning. Both lines begin at around 0.5275 intentionality, peak at approximately 0.5475 at “medium stochasticity” (0.6), where there is a balanced mix of predictability and unpredictability, and then decline as stochasticity approaches 1.0. The main difference is that the red line represents a more optimized response, showing that adaptive learning has resulted in more controlled and predictable behavior while maintaining the relationship between “stochasticity” and “intentionality”.</p>
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<p>Neuromorphic circuit design.</p>
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<p>Quantum-neuromorphic circuit design.</p>
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<p>Quantum-neuromorphic circuit simulation.</p>
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<p>The data sonification of the quantum-neuromorphic circuit simulation. Note: The ‘x’ symbols in (<b>A</b>) mark the peak amplitudes of the quantum-neuromorphic circuit’s waveform, indicating moments of maximum oscillation in the system’s behavior. (Download the file at <a href="https://github.com/jphernandezrn/Data-Sonification-Human-Robot-Interaction" target="_blank">https://github.com/jphernandezrn/Data-Sonification-Human-Robot-Interaction</a>).</p>
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8 pages, 1863 KiB  
Article
New Interpretations of the Adsorption Process of Tetracycline on Biochar via Experimental and Theoretical Studies
by Manel Ben Yahia and Lotfi Sellaoui
Water 2022, 14(23), 3821; https://doi.org/10.3390/w14233821 - 23 Nov 2022
Viewed by 1363
Abstract
A theoretical interpretation of the adsorption mechanism of tetracycline (TCCN) on biochar either in raw form (ADS1) or modified by chitosan-Fe/S (ADS2) is reported in the paper. An interpretative model is applied to the adsorption dataset, and considers that the adsorption of TCCN [...] Read more.
A theoretical interpretation of the adsorption mechanism of tetracycline (TCCN) on biochar either in raw form (ADS1) or modified by chitosan-Fe/S (ADS2) is reported in the paper. An interpretative model is applied to the adsorption dataset, and considers that the adsorption of TCCN occurs with the formation of two layers on the investigated adsorbent. The theoretical model allows good data interpretation, confirming that TCCN adsorption capacity increases with temperature. The adsorption capacity at saturation (ACS) of TCCN on the ADS1 varied from 61.91 to 91.01 mg/g. while for ADS2 it varied from 135.76 to 202.50 mg/g. This difference is probably related to the difference in adsorbent properties and to the beneficial effect exerted by the adsorbent modification. Modeling results show also that TCCN is removed via a non-parallel orientation on both ADS1 and ADS2. For a thorough analysis of this mechanism, all adsorption energies (TCCN-ADS1, ADS2, and TCCN-TCCN) are determined at different temperatures. Full article
(This article belongs to the Section Wastewater Treatment and Reuse)
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Figure 1

Figure 1
<p>Adsorption data of TCCN on ADS1 and ADS2 at different temperatures.</p>
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<p>Impact of temperature on ACS of TTCCN for both the adsorbents.</p>
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<p>Impact of temperature on the parameter <span class="html-italic">n</span>.</p>
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<p>Impact of temperature on the parameter <span class="html-italic">D<sub>RS</sub></span>.</p>
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<p>Trend of adsorption energies as a function of temperature.</p>
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<p>Examples of adsorption data fitting; (<b>a</b>) TCCN-ADS1 (<b>b</b>) TCCN-ADS2.</p>
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18 pages, 3794 KiB  
Article
Self-Assembly 2D Ti3C2/g-C3N4 MXene Heterojunction for Highly Efficient Photocatalytic Degradation of Tetracycline in Visible Wavelength Range
by Chunmin Li, Changjie Kan, Xiangtai Meng, Mengxue Liu, Qianqian Shang, Yikai Yang, Yu Wang and Xiaoxue Cui
Nanomaterials 2022, 12(22), 4015; https://doi.org/10.3390/nano12224015 - 15 Nov 2022
Cited by 9 | Viewed by 2435
Abstract
An ultrathin 2D Ti3C2/g-C3N4 MXene (2D-TC/CN) heterojunction was synthesized, using a facile self-assembly method; the perfect microscopic-morphology and the lattice structure presented in the sample with a 2 wt% content of Ti3C2 were [...] Read more.
An ultrathin 2D Ti3C2/g-C3N4 MXene (2D-TC/CN) heterojunction was synthesized, using a facile self-assembly method; the perfect microscopic-morphology and the lattice structure presented in the sample with a 2 wt% content of Ti3C2 were observed by the field-emission scanning electron microscopy (SEM) and transmission electron microscope (TEM). The optimized sample (2-TC/CN) exhibited excellent performance in degrading the tetracycline (TC), and the degradation rate reached 93.93% in the conditions of 20 mg/L, 50 mL of tetracycline within 60 min. Except for the increased specific-surface area, investigated by UV-vis diffuse reflectance spectra (UV-vis DRS) and X-ray photoelectron microscopy (XPS) valence spectra, the significantly enhanced photocatalytic activity of the 2-TC/CN could also be ascribed to the formation of Ti-N bonds between Ti3C2 and g-C3N4 nanosheets, which reduced the width of the band gap through adjusting the position of the valence band, thus resulting in the broadened light-absorption. Furthermore, the facilitated electron transmission was also proved by time-resolved photoluminescence (TRPL) and electrochemical impedance spectroscopy (EIS), which is effective in improving the quantum efficiency of photo-generated electrons. In addition, the resulting radical-capture experiment suggested that superoxide radicals have the greatest influence on photodegradation performance, with the photodegradation rate of TC reducing from 93.16% to 32.08% after the capture of superoxide radicals, which can be attributed to the production of superoxide radicals only, by the 2-TC/CN composites with a high conduction-band value (−0.62 eV). These facilely designed 2D Ti3C2/g-C3N4 composites possess great application potential for the photodegradation of tetracycline and other antibiotics. Full article
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Figure 1

Figure 1
<p>FESEM images of (<b>a</b>): multilayer Ti<sub>3</sub>C<sub>2</sub> MXene, (<b>b</b>): monolayer Ti<sub>3</sub>C<sub>2</sub> MXene and the Tyndall effect in illustration, (<b>c</b>): sheet g-C<sub>3</sub>N<sub>4</sub>, and (<b>d</b>): 2-TC/CN.</p>
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<p>(<b>a</b>) TEM image of 2-TC/CN, (<b>b</b>) HRTEM image of 2-TC/CN, (<b>c</b>) EDS mapping images of C, N, O, F, and Ti elements.</p>
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<p>(<b>a</b>) XRD patterns of Ti<sub>3</sub>AlC<sub>2</sub> and Ti<sub>3</sub>C<sub>2</sub>, (<b>b</b>) XRD patterns of g-C<sub>3</sub>N<sub>4</sub> and TC/CN, (<b>c</b>) FTIR spectra of g-C<sub>3</sub>N<sub>4</sub> and TC/CN, (<b>d</b>) XPS survey of g-C<sub>3</sub>N<sub>4</sub> and 2-TC/CN, (<b>e</b>) high-resolution XPS spectra of C1s, (<b>f</b>) high-resolution XPS of N1s, (<b>g</b>) high-resolution XPS of Ti 2p.</p>
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<p>Diffuse reflectance spectra of g-C<sub>3</sub>N<sub>4</sub> (<b>a</b>), XPS valence-band spectra (<b>b</b>), band structure (<b>c</b>) and electron paramagnetic resonance (EPR) spectra (<b>d</b>), of g-C<sub>3</sub>N<sub>4</sub> and (1-5)-TC/CN.</p>
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<p>(<b>a</b>) Photodegradation of tetracycline by g-C<sub>3</sub>N<sub>4</sub> and 1-TC/CN, 2-TC/CN, 3-TC/CN, 5-TC/CN, (<b>b</b>) the effect of IPA, EDTA-2Na and quinone on the photodegradation of tetracycline, spin-trapping EPR spectra of g-C<sub>3</sub>N<sub>4</sub> and 1-TC/CN, 2-TC/CN, 3-TC/CN, 5-TC/CN (<b>c</b>) in aqueous dispersion and (<b>d</b>) in methanol dispersion after light irradiation, using DMPO as a radical-trapping agent.</p>
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<p>(<b>a</b>) Room-temperature PL spectra, (<b>b</b>) transient fluorescence-emission spectra, (<b>c</b>) transient photocurrent responses, (<b>d</b>) EIS spectra, of as-prepared samples.</p>
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<p>Schematic diagram of the preparation process of 2D Ti<sub>3</sub>C<sub>2</sub>/g-C<sub>3</sub>N<sub>4</sub> MXene composite materials.</p>
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<p>Diagram of photodegradation mechanism of tetracycline.</p>
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21 pages, 17410 KiB  
Article
Theranostic Tripartite Cancer Terminator Virus for Cancer Therapy and Imaging
by Praveen Bhoopathi, Anjan K. Pradhan, Santanu Maji, Swadesh K. Das, Luni Emdad and Paul B. Fisher
Cancers 2021, 13(4), 857; https://doi.org/10.3390/cancers13040857 - 18 Feb 2021
Cited by 6 | Viewed by 2474
Abstract
Combining cancer-selective viral replication and simultaneous production of a therapeutic cytokine, with potent “bystander” anti-tumor activity, are hallmarks of the cancer terminator virus (CTV). To expand on these attributes, we designed a next generation CTV that additionally enables simultaneous non-invasive imaging [...] Read more.
Combining cancer-selective viral replication and simultaneous production of a therapeutic cytokine, with potent “bystander” anti-tumor activity, are hallmarks of the cancer terminator virus (CTV). To expand on these attributes, we designed a next generation CTV that additionally enables simultaneous non-invasive imaging of tumors targeted for eradication. A unique tripartite CTV “theranostic” adenovirus (TCTV) has now been created that employs three distinct promoters to target virus replication, cytokine production and imaging capabilities uniquely in cancer cells. Conditional replication of the TCTV is regulated by a cancer-selective (truncated PEG-3) promoter, the therapeutic component, MDA-7/IL-24, is under a ubiquitous (CMV) promoter, and finally the imaging capabilities are synchronized through another cancer selective (truncated tCCN1) promoter. Using in vitro studies and clinically relevant in vivo models of breast and prostate cancer, we demonstrate that incorporating a reporter gene for imaging does not compromise the exceptional therapeutic efficacy of our previously reported bipartite CTV. This TCTV permits targeted treatment of tumors while monitoring tumor regression, with potential to simultaneously detect metastasis due to the cancer-selective activity of reporter gene expression. This “theranostic” virus provides a new genetic tool for distinguishing and treating localized and metastatic cancers. Full article
(This article belongs to the Special Issue Feature Paper from Journal Reviewers)
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Figure 1

Figure 1
<p>Construction and characterization of Ad.5-<span class="html-italic">TCTV</span>. (<b>A</b>) Schematic diagram representing the gene sequence in the vector used to generate the <span class="html-italic">TCTV</span>. A truncated <span class="html-italic">PEG</span>-Prom drives type 5 adenovirus replication and a truncated <span class="html-italic">tCCN1</span>-Prom drives luciferase expression. (<b>B</b>) Schematic representation of the cloning procedure used to construct the Ad.5-<span class="html-italic">TCTV</span>. (<b>C</b>) MDA-MB-231 and DU-145 cells were infected with either Ad.5-<span class="html-italic">E1A</span> (25 pfu), Ad.5-<span class="html-italic">CTV</span> (25 pfu), or Ad.5-<span class="html-italic">TCTV</span> (25 pfu) for 48 h. Total RNA was extracted using Trizol reagent, and reverse transcriptase PCR was performed for assessment of <span class="html-italic">mda-7/IL-24</span> mRNA transcript levels. <span class="html-italic">GAPDH</span> served as a loading control. (<b>D</b>) Western blotting for E1A and MDA-7/IL-24 protein expression was done using cell lysates with specific antibodies.</p>
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<p>Ad.5-<span class="html-italic">TCTV</span> inhibits cancer cell proliferation to a similar extent as Ad.5-<span class="html-italic">CTV</span>. (<b>A</b>–<b>D</b>) The indicated cell types (5000 cells), (<b>A</b>) human breast cancer (MDA-MB-231 and SUM-159); (<b>B</b>) human prostate cancer (DU-145 and PC-3); (<b>C</b>) primary normal human breast epithelial (HMEC); and (<b>D</b>) normal immortal prostate epithelial (RWPE-1) cells were plated in 96-well plates and infected with either Ad.5-<span class="html-italic">E1A</span> (25 pfu), Ad.5-<span class="html-italic">CTV</span> (25 pfu), or Ad.5-<span class="html-italic">TCTV</span> (25 pfu) for 72 h. These cells were then treated with 20 μL of MTT in phosphate-buffered saline (PBS) and incubated further for 4 h. Media was then removed and formazan crystals were dissolved using dimethyl sulphoxide (DMSO) (100 μL). A microplate reader was used to measure the absorbance at 550 nm and the results are presented as percent proliferation with the comparison of cells treated with vehicle. Points, mean of triplicate experiments; bars, S.E. * <span class="html-italic">p</span> &lt; 0.05 vs. control.</p>
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<p>Ad.5-<span class="html-italic">TCTV</span> induces ER stress and apoptosis in cancer cells. (<b>A</b>) Breast cancer cells (MDA-MB-231 and SUM-159) treated with 25 pfu of Ad.5-<span class="html-italic">E1A</span> or the indicated pfu of Ad.5-<span class="html-italic">CTV</span> or Ad.5-<span class="html-italic">TCTV</span> for 72 h. Cells were then collected and Western blotting analysis was performed for signaling molecules using specific antibodies and β-actin served as a loading control. (<b>B</b>) Breast cancer cells were cultured in 8-well chamber slides and infected with 25 pfu of Ad.5-<span class="html-italic">E1A</span>, Ad.5-<span class="html-italic">CTV,</span> or Ad.5-<span class="html-italic">TCTV</span> for 72 h. Cells were fixed and TUNEL assays were performed. Data presented as TUNEL positive cells in a defined microscopic field as compared with un-treated control cells. (<b>C</b>) Prostate cancer cells (DU-145 and PC-3) were treated as described in <b>A</b>, cells were then collected and Western blotting analysis was performed for signaling molecules using specific antibodies and β-actin served as a loading control. (<b>D</b>) Prostate cancer cells were treated as described in <b>B</b> and cells were fixed and TUNEL assays were performed. Data presented as TUNEL positive cells in a defined microscopic field as compared with un-treated control cells. Scale bar: 200 μM.</p>
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<p>The <span class="html-italic">TCTV</span> does not induce apoptosis in normal breast and prostate epithelial cells. Normal primary breast epithelial (HMEC) and normal immortal prostate epithelial (RWPE-1) cells were cultured in 8-well chamber slides and treated with 25 pfu of Ad.5-<span class="html-italic">E1A</span>, Ad.5-<span class="html-italic">CTV,</span> or Ad.5-<span class="html-italic">TCTV</span> for 72 h. Cells were fixed and TUNEL assays were performed. Data presented as TUNEL positive cells in a defined microscopic field as compared with the un-treated control cells. Scale bar: 200 μM.</p>
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<p>Ad.5-<span class="html-italic">TCTV</span> inhibits tumor growth to a comparable level of Ad.5-<span class="html-italic">CTV</span> and additionally permits non-invasive imaging of tumor growth <span class="html-italic">in vivo</span>. MDA-MB-231 (breast) and mu-Hi-Myc PDX (prostate) cancer cells were implanted subcutaneously in the lower and upper flanks of nude mice and lower tumors were treated with eight intratumoral injections of solvent (mock treatment-Control), Ad.5-<span class="html-italic">E1A</span>, Ad.5-<span class="html-italic">CTV,</span> or Ad.5-<span class="html-italic">TCTV</span>. A total of five animals were studied in each group. Once the tumors in untreated mice reached maximum IACUC acceptable limits, mice were euthanized and tumors were collected, fixed in formalin, and embedded in paraffin. (<b>A</b> and <b>C</b>) Tumor volumes from the lower (injected tumors) and upper flanks (un-injected tumors) were measured and the results are presented in a graphical manner. The line represents average of all tumor volumes of the group. * <span class="html-italic">p</span> &lt; 0.05 vs. control, ns: no significant difference between Ad.5-<span class="html-italic">CTV</span> or Ad.5-<span class="html-italic">TCTV</span> group. (<b>B</b> and <b>D</b>) Ad.5-<span class="html-italic">TCTV</span> injected tumors were visualized using BLI (IVIS imager). Inset, BLI image of un-injected tumors following injection of lower flank tumor with Ad.5-<span class="html-italic">TCTV.</span></p>
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<p>Ad.5-<span class="html-italic">TCTV</span> inhibits tumor growth in the MMTV-PyMT model. Mice treated intratumorally with Ad.5-<span class="html-italic">CTV</span> as described in methods or untreated controls were monitored for tumor burden over 4-weeks following first appearance of tumors. (<b>A</b>) Shown are representative photographs of tumors present in MMTV-PyMT mice untreated or treated with Ad.5-<span class="html-italic">TCTV</span> at the time of euthanasia. In each of the images, image dimensions are adjusted roughly to match the scale. (<b>B</b>) Tumor volumes and weights were quantified and the average tumor volume and total tumor weight are presented in a graphical manner. * <span class="html-italic">p</span> &lt; 0.05 vs. control. (<b>C</b>) Immunohistochemical analysis of MDA-7/IL-24 in control and Ad.5-<span class="html-italic">TCTV</span> treated tumor sections.</p>
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<p>Ad.5-<span class="html-italic">TCTV</span> induces apoptosis and inhibits angiogenesis in vivo. MDA-MB 231 and mu-Hi-Myc PDX cancer cells were implanted subcutaneously in the lower and upper flanks of nude mice and the lower tumors were treated with eight intratumoral injections including solvent (mock treated control), Ad.5-<span class="html-italic">E1A</span> or Ad.5-<span class="html-italic">CTV</span> or Ad.5-<span class="html-italic">TCTV</span>. A total of five animals were studied in each group. Once the control animals’ tumors reached maximum allowable limit, tumors were collected, fixed in formalin, and embedded in paraffin. (<b>A</b>) Immunohistochemical (IHC) analysis of MDA-7/IL-24, adenovirus E1A, and Luciferase from tumor sections as indicated. (<b>B</b>) IHC analysis of Bcl-2 and CD-31 from tumor sections as indicated. Scale bar: 200 μM.</p>
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<p>Ad.5-<span class="html-italic">CTV</span> and Ad.5-<span class="html-italic">TCTV</span> induces ER stress (GRP-78) and apoptosis (TUNEL) in breast and prostate tumors in nude mice. (<b>A</b>) MDA-MB 231 and mu-Hi-Myc PDX cancer cells were implanted subcutaneously in the lower and upper flanks of nude mice and lower tumors were infected with the indicated virus. A total of five animals were studied in each group. Once the control animals’ tumors reached maximum allowable limit, tumors were collected fixed in formalin and embedded in paraffin. TUNEL assays were performed according to the manufacturers protocol. Nuclei were stained with DAPI. Photographs were taken in ten random microscopic fields and representative pictures are shown. (<b>B</b>) Formalin and embedded in paraffin samples as prepared in <b>A</b> above, were stained for GRP-78 (an ER stress marker) and nuclei were stained with DAPI. Scale bar: 50 μM.</p>
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