Publications by authors named "Jinxin Tao"

To measure the combustion parameters of a solid propellant, this Letter researches the fitting method for flame temperature and emissivity based on multispectral images and proposes the particle swarm optimization-K-means (PSO-K-means) clustering optimization algorithm of a flame multispectral image. Considering the difference in flame radiation characteristics in different regions, the flame multispectral image is clustered, and spectra in different regions are analyzed and selected in different fitting bands to inverse temperature and emissivity. On this basis, the method is applied to measure solid propellant combustion parameters with different formulations.

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Article Synopsis
  • * Researchers identified CALB2 as a key protein that is highly expressed in cancer-associated fibroblasts (CAFs) and cancer cells, which is linked to worse patient outcomes and an immunosuppressive tumor microenvironment.
  • * The findings revealed that CALB2, in conjunction with hypoxia, promotes an inflammatory fibroblast phenotype that enhances cancer cell migration and growth, indicating its potential role in PDAC metastasis and the development of inflammation-targeted treatments.
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Background: Hypertension is the most common reason for postpartum hospital readmission. Better prediction of postpartum readmission will improve the health care of patients. These models will allow better use of resources and decrease health care costs.

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Metastatic clear cell renal cell carcinoma has heterogenous tumor microenvironment (TME). Among the metastatic lesions, pancreas metastasis is rare and controversy in treatment approaches. Here, extensive primary and metastatic lesion samples were included by single-cell RNA-seq to decipher the distinct metastasis TME.

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Pancreatic ductal adenocarcinoma (PDAC) is a highly aggressive malignancy with a poor prognosis and limited therapeutic options. Research on the tumor microenvironment (TME) of PDAC has propelled the development of immunotherapeutic and targeted therapeutic strategies with a promising future. The emergence of single-cell sequencing and mass spectrometry technologies, coupled with spatial omics, has collectively revealed the heterogeneity of the TME from a multiomics perspective, outlined the development trajectories of cell lineages, and revealed important functions of previously underrated myeloid cells and tumor stroma cells.

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Pancreatic ductal adenocarcinoma (PDAC) is one of the leading causes of cancer-related death worldwide, primarily due to its rapid progression. The current treatment options for PDAC are limited, and a better understanding of the underlying mechanisms responsible for PDAC progression is required to identify improved therapeutic strategies. In this study, we identified FBXO32 as an oncogenic driver in PDAC.

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Pancreatic ductal adenocarcinoma (PDAC) is a highly malignant neoplasm characterized by a poor prognosis and limited therapeutic strategy. The PDAC tumor microenvironment presents a complex heterogeneity, where neutrophils emerge as the predominant constituents of the innate immune cell population. Leveraging the power of single-cell RNA-seq, spatial RNA-seq, and multi-omics approaches, we included both published datasets and our in-house patient cohorts, elucidating the inherent heterogeneity in the formation of neutrophil extracellular traps (NETs) and revealed the correlation between NETs and immune suppression.

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Ferroptosis, a novel form of iron-dependent non-apoptotic cell death, plays an active role in the pathogenesis of diverse diseases, including cancer. However, the mechanism through which ferroptosis is regulated in pancreatic ductal adenocarcinoma (PDAC) remains unclear. Here, our study, via combining bioinformatic analysis with experimental validation, showed that ferroptosis is inhibited in PDAC.

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Nuclear factor kappa B (NF-κB) plays a pivotal role in the development of pancreatic cancer, and its phosphorylation has previously been linked to the regulation of NUAK2. However, the regulatory connection between NF-κB and NUAK2, as well as NUAK2's role in pancreatic cancer, remains unclear. In this study, we observed that inhibiting NUAK2 impeded the proliferation, migration, and invasion of pancreatic cancer cells while triggering apoptosis.

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Background: Hypertensive disorders of pregnancy are one of the leading causes of maternal morbidity and mortality worldwide. Management of these conditions can pose many clinical dilemmas and can be particularly challenging during the immediate postpartum period. Models for predicting and managing postpartum hypertension are necessary to help address this clinical challenge.

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Neoplastic cells need to adapt their gene expression pattern to survive in an ever-changing or unfavorable tumor microenvironment. Protein synthesis (or mRNA translation), an essential part of gene expression, is dysregulated in cancer. The emergence of distinct translatomic technologies has revolutionized oncological studies to elucidate translational regulatory mechanisms.

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Pancreatic cancer (PC) is a devastating malignancy with an extremely high mortality rate and poses significant challenges to healthcare systems worldwide. The prevalence of PC risk factors spiked over the years, leading to a global increase in PC incidence rates. The contribution of different risk factors, however, varied from region to region due to genetic predisposition, environmental, social, and political factors underlying disease prevalence in addition to public health strategies.

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Pancreatic cancer (PC) is considered highly malignant due to its unsatisfying prognosis and limited response to therapies. Immunotherapy has therefore been developed to harness the antigen-specific properties and cytotoxicity of the immune system, aiming to induce a robust anti-tumor immune response that specifically demolishes PC cells while minimizing lethality in healthy tissue. The activation and augmentation of cytotoxic T cells play a critical role in the initiation and final success of immunotherapy.

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Purpose: This study aims to review the multifaceted roles of a membrane protein named Fibroblast Activation Protein (FAP) expressed in tumor tissue, including its molecular functionalities, regulatory mechanisms governing its expression, prognostic significance, and its crucial role in cancer diagnosis and treatment.

Methods: Articles that have uncovered the regulatory role of FAP in tumor, as well as its potential utility within clinical realms, spanning diagnosis to therapeutic intervention has been screened for a comprehensive review.

Results: Our review reveals that FAP plays a pivotal role in solid tumor progression by undertaking a multitude of enzymatic and nonenzymatic roles within the tumor stroma.

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Nowadays, the diagnosis and treatment system of malignant tumors has increasingly tended to be more precise and personalized while the existing tumor models are still unable to fully meet the needs of clinical practice. Notably, the emerging organoid platform has been proven to have huge potential in the field of basic-translational medicine, which is expected to promote a paradigm shift in personalized medicine. Here, given the unique advantages of organoid platform, we mainly explore the prominent role of organoid models in basic research and clinical practice from perspectives of tumor biology, tumorigenic microbes-host interaction, clinical decision-making, and regenerative strategy.

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Objective: Pancreatic cancer (PC) is highly malignant, but the underlying mechanisms of cancer progression remain unclear. PRKRA is involved in cellular stress response, but its role in PC was unknown.

Methods: The expression of PRKRA between normal and tumor tissues were compared, and the prognostic value of PRKRA was evaluated.

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Article Synopsis
  • * Researchers used advanced methods to identify these subtypes, leading to the creation of a risk score that categorizes patients into high- and low-risk groups, improving survival predictions.
  • * Specific oncogenes, such as FAM83A and KLF5, were found to be linked to cancer cell proliferation, suggesting that targeting these genes could offer new treatment options for pancreatic cancer.
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Persistent human papilloma virus (HPV) infection is known to be associated with cervical lesions. The chief object of the study is to investigate if the pathogenicity of multiple HPV infections is different from a single infection. Furthermore, we would like to corroborate the discrepancy with clearance rates.

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Purpose: This study aimed to investigate male HPV infection, re-examination rate, clearance rate and relevant influencing factors as well as HPV infection between heterosexual partners in Wenzhou, China.

Methods: The study enrolled 2359 men who accepted ≥1 HPV detection in the First Affiliated Hospital of Wenzhou Medical University between June 2014 and June 2020. An outpatient follow-up was carried out for collecting HPV re-test results among males who were tested HPV positive.

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Aims: This study aimed to investigate the prognostic value of clinical features for cancer-specific survival (CSS) and metastasis in patients with pancreatic mucinous cystadenocarcinoma (MCAC). We further constructed and validated an effective nomogram to predict CSS.

Methods: We screened patients diagnosed with pancreatic MCAC from Surveillance Epidemiology and End Results (SEER) database.

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Article Synopsis
  • Pancreatic ductal adenocarcinoma (PDAC) shows poor response to gemcitabine, a common chemotherapy, with stanniocalcin-1 (STC1) identified as a gene linked to resistance.
  • Research used methods like RT-qPCR and Western blot to study STC1's role in PDAC, revealing that it mediates chemoresistance through HIF-1α and activates the PI3K/AKT signaling pathway.
  • Analysis indicated that high STC1 levels are associated with worse outcomes in patients treated with gemcitabine after surgery, suggesting STC1 could be a potential prognostic marker and treatment target for PDAC.
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As a domain adaptation method, the domain-adversarial neural network (DANN) can utilize the adversarial learning of the feature extractor and domain discriminator to extract the domain-invariant features, thus realizing fault identification of rolling bearings. In the cross-domain diagnosis of rolling bearing faults, how to obtain fault-related discriminative domain-invariant features from the noisy signals is a key to improving the diagnostic result. In response to this, this paper proposes an intelligent diagnosis model based on the DANN and attention mechanism to identify rolling bearing faults.

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Pancreatic cancer (PC) is a highly aggressive gastrointestinal tumor and has a poor prognosis. Evaluating the prognosis validly is urgent for PC patients. In this study, we utilized the RNA-sequencing (RNA-seq) profiles and DNA methylation expression data comprehensively to develop and validate a prognostic signature in patients with PC.

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Pancreatic cancer (PC) is an increasingly common disease worldwide. Having a better understanding of worldwide and regional epidemiologic features and risk factors of PC is essential to identify new approaches for prevention, early diagnosis, surveillance, and treatment. In this article, we review the epidemiologic features and risk factors for PC and discuss opportunities and challenges of PC future treatment.

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Synopsis of recent research by authors named "Jinxin Tao"

  • - Jinxin Tao's recent research primarily focuses on understanding the tumor microenvironment (TME) in pancreatic cancer, investigating its roles in disease progression, metastasis, and therapeutic resistance, which is critical for developing personalized treatment strategies.
  • - The studies employ advanced methodologies including single-cell RNA sequencing and multiomics approaches to decipher TME heterogeneity and identify novel prognostic biomarkers, providing insights into immune cell dynamics and potential therapeutic targets for pancreatic ductal adenocarcinoma (PDAC).
  • - Additionally, Tao's work extends to addressing public health issues by predicting postpartum hypertension readmissions, thereby highlighting the integration of machine learning models in improving patient outcomes in obstetrics alongside cancer research.