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Yuxia Tang

Publications and source records attributed to Yuxia Tang.

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DAMM-Diffusion: Learning Divergence-Aware Multi-Modal Diffusion Model for Nanoparticles Distribution Prediction

The prediction of nanoparticles (NPs) distribution is crucial for the diagnosis and treatment of tumors. Recent studies indicate that the heterogeneity of tumor microenvironment (TME) highly affects the distribution of NPs across tumors. Hence, it has become a research hotspot to generate the NPs distribution by the aid of multi-modal TME components. However, the distribution divergence among multi-modal TME components may cause side effects i.e., the best uni-modal model may outperform the joint generative model. To address the above issues, we propose a \textbf{D}ivergence-\textbf{A}ware \textbf{M}ulti-\textbf{M}odal \textbf{Diffusion} model (i.e., \textbf{DAMM-Diffusion}) to adaptively generate the prediction results from uni-modal and multi-modal branches in a unified network. In detail, the uni-modal branch is composed of the U-Net architecture while the multi-modal branch extends it by introducing two novel fusion modules i.e., Multi-Modal Fusion Module (MMFM) and Uncertainty-Aware Fusion Module (UAFM). Specifically, the MMFM is proposed to fuse features from multiple modalities, while the UAFM module is introduced to learn the uncertainty map for cross-attention computation. Following the individual prediction results from each branch, the Divergence-Aware Multi-Modal Predictor (DAMMP) module is proposed to assess the consistency of multi-modal data with the uncertainty map, which determines whether the final prediction results come from multi-modal or uni-modal predictions. We predict the NPs distribution given the TME components of tumor vessels and cell nuclei, and the experimental results show that DAMM-Diffusion can generate the distribution of NPs with higher accuracy than the comparing methods. Additional results on the multi-modal brain image synthesis task further validate the effectiveness of the proposed method.

cs.CV

Multimodal Radiomics Model for Predicting Gold Nanoparticles Accumulation in Mouse Tumors

Background: Nanoparticles can accumulate in solid tumors, serving as diagnostic or therapeutic agents for cancer. Clinical translation is challenging due to low accumulation in tumors and heterogeneity between tumor types and individuals. Tools to identify this heterogeneity and predict nanoparticle accumulation are needed. Advanced imaging techniques combined with radiomics and AI may offer a solution. Methods: 183 mice were used to create seven subcutaneous tumor models, with three sizes (15nm, 40nm, 70nm) of gold nanoparticles injected via the tail vein. Accumulation was measured using ICP-OES. Data were divided into training and test sets (7:3). Tumors were categorized into high and low uptake groups based on the median value of the training set. Before injection, multimodal imaging data (CT, B-mode ultrasound, SWE, CEUS) were acquired, and radiomics features extracted. LASSO and RFE algorithms built a radiomics signature. This, along with tumor type and mean values from CT and SWE, constructed the best model using SVM. For each tumor in the test set, the radiomics signature predicted gold nanoparticle uptake. Model performance was evaluated by AUC. Results: Significant variability in gold nanoparticle accumulation was observed among tumors (P < 0.001). The median accumulation in the training set was 3.37% ID/g. Nanoparticle size was not a main determinant of uptake (P > 0.05). The composite model based on radiomics signature outperformed the basic model in both training (AUC 0.93 vs. 0.68) and testing (0.78 vs. 0.61) datasets. Conclusion: The composite model identifies tumor heterogeneity and predicts high uptake of gold nanoparticles, improving patient stratification and supporting nanomedicine's clinical application.

q-bio.QM

High-throughput screening of quaternary compounds and new insight for excellent thermoelectric performance

It is well known that the high electric conductivity, large Seebeck coefficient, and low thermal conductivity are preferred for enhancing thermoelectric performance, but unfortunately, these properties are strongly inter-correlated with no rational scenario for their efficient decoupling. This big dilemma for thermoelectric research appeals for alternative strategic solutions, while the high-throughput screening is one of them. In this work, we start from total 3136 real electronic structures of the huge X2YZM4 quaternary compound family and perform the high-throughput searching in terms of enhanced thermoelectric properties. The comprehensive data-mining allows an evaluation of the electronic and phonon characteristics of those promising thermoelectric materials. More importantly, a new insight that the enhanced thermoelectric performance benefits substantially from the coexisting quasi-Dirac and heavy fermions plus strong optical-acoustic phonon hybridization, is proposed. This work provides a clear guidance to theoretical screening and experimental realization and thus towards development of performance-excellent thermoelectric materials.

physics.app-ph

GANDA: A deep generative adversarial network predicts the spatial distribution of nanoparticles in tumor pixelly

Intratumoral nanoparticles (NPs) distribution is critical for the success of nanomedicine in imaging and treatment, but computational models to describe the NPs distribution remain unavailable due to the complex tumor-nano interactions. Here, we develop a Generative Adversarial Network for Distribution Analysis (GANDA) to describe and conditionally generates the intratumoral quantum dots (QDs) distribution after i.v. injection. This deep generative model is trained automatically by 27 775 patches of tumor vessels and cell nuclei decomposed from whole-slide images of 4T1 breast cancer sections. The GANDA model can conditionally generate images of intratumoral QDs distribution under the constraint of given tumor vessels and cell nuclei channels with the same spatial resolution (pixels-to-pixels), minimal loss (mean squared error, MSE = 1.871) and excellent reliability (intraclass correlation, ICC = 0.94). Quantitative analysis of QDs extravasation distance (ICC = 0.95) and subarea distribution (ICC = 0.99) is allowed on the generated images without knowing the real QDs distribution. We believe this deep generative model may provide opportunities to investigate how influencing factors affect NPs distribution in individual tumors and guide nanomedicine optimization for molecular imaging and personalized treatment.

eess.IV