Publications by authors named "Pan Lili"

Esophageal leiomyoma is the most common benign intramural tumor of the esophagus. Despite being the most common benign tumor in its category, esophageal leiomyomas constitute only 1.2% of all esophageal tumors.

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  • Triple-negative breast cancer (TNBC) is a highly aggressive type of breast cancer with limited treatment options, as it doesn't respond to hormonal or targeted therapies.
  • Current standard treatment involves chemotherapy, which often fails due to the cancer's high recurrence rates after surgery.
  • Researchers have developed a new treatment using gold nanoclusters for photothermal and chemodynamic therapy, showing promising results in inhibiting tumors and enhancing immune responses, making it a potentially effective option for TNBC.
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Malignant tumors pose substantial treatment challenges due to their heterogeneity, metastatic potential, and therapeutic resistance, underscoring the urgent need for more effective treatment options. In this study, a novel radionuclide drug conjugate (RDC) was developed and characterized employing a tumor-targeting heptamethine carbocyanine dye (DZ) for its high specificity and favourable safety profile. The RDC, DOTA-DZ-HX, was synthesized by conjugating DZ with dodecane tetraacetic acid (DOTA) through a dipeptide linker.

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Background: Takayasu arteritis (TA) is associated with an increased risk of developing complicated comorbidities, which can bring both psychological and physical burdens to the patients.

Objective: TA is found to carry a high risk of developing depression. This research aimed to investigate the risk factors and prognosis of depression in TA patients.

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RNA modification has emerged as an important epigenetic mechanism that controls abnormal metabolism and growth in acute myeloid leukaemia (AML). However, the roles of RNA N-acetylcytidine (ac4C) modification in AML remain elusive. Here, we report that ac4C and its catalytic enzyme NAT10 drive leukaemogenesis and sustain self-renewal of leukaemic stem cells/leukaemia-initiating cells through reprogramming serine metabolism.

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On December 1st, 2022, the FDA approved the new molecular entity olutasidenib (Rezlidhia: Rigel Pharmaceuticals), a small-molecule inhibitor of isocitrate dehydrogenase-1 (IDH1), for the treatment of adult patients with relapsed or refractory acute myeloid leukemia (R/R AML) with a susceptible IDH1 mutation as detected by an FDA-approved test. The efficacy of olutasidenib was established based on complete remission (CR) + CR with partial hematological recovery (CRh) rate, duration of CR + CRh, and conversion of transfusion dependence (TD) to transfusion independence (TI) in Study 2102-HEM-101. In the pivotal trial, 147 adult patients treated with 150mg twice daily (BID) of olutasidenib were evaluable for efficacy.

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  • Coronary artery involvement (CAI) is a notable yet not uncommon outcome of Takayasu arteritis (TAK), and this study aimed to explore the role of Granzyme B (GzmB) in patients with TAK and CAI.
  • The research included 105 TAK patients and 58 healthy controls, finding significant differences in various health metrics and an increased presence of certain immune cell types (CD3+CD8+ and CD3+CD4+) among TAK patients with CAI.
  • The study concluded that a higher ratio of CD3+CD8+GzmB+ cells in lymphocytes could serve as an independent risk factor for CAI and major adverse cardiovascular events (MACE), suggesting that targeting
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On December 14, 2022, the FDA approved revisions to the United States Prescribing Information (USPI) for capecitabine that revised existing indications and dosage regimens, added new indications and their recommended dosage regimens, revised safety information, updated the description of the risk of capecitabine in patients with dihydropyrimidine dehydrogenase deficiency, and edited other sections of the USPI to conform with FDA's current labeling guidance. These supplements were reviewed and approved under Project Renewal, a public health initiative established by the FDA's Oncology Center of Excellence that aims to update the prescribing information of certain older oncology drugs to ensure information is clinically meaningful and scientifically up to date. This article summarizes the FDA approach that supported revisions to the capecitabine USPI within the context of Project Renewal.

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Purpose: To investigate the prevalence and characteristics of late gadolinium enhancement (LGE) by cardiac magnetic resonance (CMR) and its prognostic value in patients with Takayasu arteritis (TA).

Materials And Methods: Sixty TA patients with a CMR examination were retrospectively included. All TA patients were divided into with LGE-positive and LGE-negative groups.

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Background: The prevalence of online altruistic behaviors among the college students has attracted widespread attention. However, the factors influencing this are still unclear. The objective of this study was to explore the relationship and mechanism of online interpersonal trust, moral identity, online social support and online altruistic behavior among college students.

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  • - Cogan's syndrome (CS) is a type of vasculitis that can cause various symptoms, including coronary artery stenosis and problems with vision and hearing.
  • - A case study of a middle-aged woman highlighted the importance of recognizing CS, as she had elevated markers in her vascular system that led to the diagnosis.
  • - The report encourages clinicians to consider CS when patients show recurrent coronary artery issues and to conduct thorough patient histories for better diagnosis.
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Anaplastic lymphoma kinase (ALK) fusion genes promote a variety of human malignancies. Although several ALK inhibitors have significantly improved disease prognosis in patients with ALK positive cancers, the persistent emergence of acquired drug-resistant mutations remain the major problem in clinic treatment. Adoption of new therapeutic strategies such as proteolysis targeting chimera (PROTAC) to overcome drug resistance in BTK/AR-related cancers have shown promising prospect.

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Background: The predictive importance of IKZF1 in pediatric B-cell precursor acute lymphoblastic leukemia (BCP-ALL) has shown variability across different studies. Thus, the optimal treatment approach for children with IKZF1 BCP-ALL remains contentious, with the ongoing debate surrounding the use of IKZF1-based high-risk stratification versus a minimal residual disease (MRD)-guided protocol.

Methods: IKZF1 status was reliably determined in 804 patients using multiplex ligation-dependent probe amplification (MLPA) data obtained from four hospitals in Fujian, a province of China.

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Objectives: The aim of this study was to investigate the predictive value of uric acid (UA) in prognosis of pulmonary artery involvement (PAI) in patients with Takayasu's arteritis (TAK).

Methods: A total of 166 TAK patients were enrolled in the study, including 76 with PAI and 90 without. Outcomes of 144 TAK patients were followed up and recorded.

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  • Dexmedetomidine is widely used in both clinical and animal studies for its sedative, analgesic, and anxiolytic properties, leading to significant interest in understanding its research trajectory over the past decade.
  • A bibliometric analysis of 5,482 relevant publications from 2014 to 2023 highlighted the United States as a leading contributor, with an emphasis on recent studies related to sedation, delirium, and opioid-free anesthesia.
  • The study identified key research frontiers including stress response and neuroinflammation, suggesting these areas will shape future investigations and clinical applications of dexmedetomidine.
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  • The heart can be affected by a disease called IgG4-related disease (IgG4-RD), which is rare but important to study.
  • In a study of 42 patients, researchers looked at the heart problems caused by this disease and how well treatments worked.
  • Most patients responded well to treatments like glucocorticoids, but some had relapses, showing that careful monitoring is needed even after treatment.
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On August 11, 2022, FDA granted accelerated approval to fam-trastuzumab deruxtecan-nxki (DS-8201a, T-DXd, ENHERTU, Daiichi Sankyo) for adult patients with unresectable or metastatic non-small cell lung cancer (NSCLC) whose tumors have activating human epidermal growth factor receptor 2 (HER2) mutations, as detected by an FDA-approved test, and who have received a prior systemic therapy. The approval was based on a prespecified interim analysis of DESTINY-Lung02 (Study U206), a multi-center, randomized, dose-optimization trial in patients with NSCLC harboring activating HER2-mutations. At the approved dose of 5.

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Targeting receptor-interacting protein kinase 1 (RIPK1) has emerged as a promising therapeutic stratagem for neurodegenerative disorders, particularly Alzheimer's disease (AD). A positron emission tomography (PET) probe enabling brain RIPK1 imaging can provide a powerful tool to unveil the neuropathology associated with RIPK1. Herein, the development of a new PET radioligand, [C]CNY-10 is reported, which may enable brain RIPK1 imaging.

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Dielectric elastomers, such as thermoplastic polyurethanes (TPUs), are widely used as the dielectric layer, encapsulation layer, and substrate of flexible and stretchable devices. To construct capacitors and actuators that work stably upon deformation, it has become urgent to investigate the evolution of dielectricity under stress and strain. However, the lack of effective methods for estimating the dielectric constant of elastomers under strain poses a big challenge.

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  • On November 15, 2023, the FDA approved repotrectinib (Augtyro) for adults with ROS1-positive non-small cell lung cancer, based on data from the TRIDENT-1 trial.
  • The trial showed an objective response rate (ORR) of 79% in patients who had not previously received ROS1 TKI treatment, while those who had showed a lower ORR of 38%.
  • Common side effects included dizziness, fatigue, and cognitive disorders, and the approval notably highlighted efficacy in patients who had progressed on previous ROS1 therapies.
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  • * Flexible magnetosensitive devices are important because they combine the benefits of flexible electronics with magnetoelectronic features like reshaping and contactless sensing.
  • * This study reviews recent advances in flexible magnetosensitive devices, covering material fabrication, sensor performance, applications in wearables, and future challenges in the field.
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Objective: The primary aim of this study is to assess the diagnostic efficacy of elastography and contrast-enhanced ultrasound (CEUS) in the identification of breast lesions subsequent to the optimization and correction of the BI-RADS category 4 classification obtained through conventional ultrasound. The objective is to augment both the specificity and accuracy of breast lesion diagnosis, thereby establishing a reliable framework for reducing unnecessary biopsies in clinical settings.

Methods: A cohort comprising 50 cases of breast lesions classified under BI-RADS category 4 was collected during the period from November 2022 and November 2023.

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Objectives: Coronary artery calcification (CAC) is frequently observed in Takayasu's arteritis (TAK). Our objective is to calculate the prevalence and severity of CAC in TAK, while evaluating the influence of traditional cardiovascular risk factors, glucocorticoid exposure, and disease activity on CAC.

Methods: This retrospective study involved 155 TAK patients.

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Objective: The goal of the present study was to investigate the correlation between serum 25-hydroxyvitamin D [25(OH)D] levels and disease remission in Takayasu arteritis (TAK) patients.

Methods: This retrospective study included 59 patients in the study group and 80 patients in the validation cohort with TAK. After 6 months of therapy, patients were re-evaluated, and serum 25(OH)D levels were compared before and after treatment.

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Introduction: Improved understanding of the prognostic biomarkers associated with childhood acute lymphoblastic leukemia (ALL) is needed for accurate risk group stratification. This study aimed to identify potential long non-coding RNA (lncRNA) markers and evaluate their prognostic value in children with ALL.

Methods: We selected 50 children with newly diagnosed ALL and 20 age-matched patients with idiopathic immune thrombocytopenia (controls).

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