Publications by authors named "Siyang Liu"

Introduction: EGFR tyrosine kinase inhibitor (TKI) is the standard adjuvant treatment for patients with stages IB to IIIA -mutated NSCLC. Nevertheless, adapting this approach to include a molecular residual disease (MRD)-guided de-escalation strategy warrants further investigation.

Methods: From January 2019 to December 2022, 71 patients with stages I to III NSCLC and (exon 19 deletion or L858R) mutations were enrolled in this observational study.

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During the COVID-19 lockdown in China, the shift of family members' work and study to online platforms accelerated internet proliferation and led to a growing prominence of internet addiction among younger age groups, posing a threat to individual and societal health development. Previous research has primarily focused on upper-grade elementary students, with relatively less attention given to younger age groups, resulting in insufficient representativeness of the elementary student samples. Additionally, research exploring how parental addictive behaviors are associated with the mechanisms of internet addiction among elementary students has been limited, which affects the development of scientifically based and effective intervention measures for addressing internet addiction in this population.

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Article Synopsis
  • Kounis syndrome is an acute coronary condition triggered by allergic reactions, resulting in heart damage and, in some cases, anaphylactic shock.
  • This syndrome can occur as a rare side effect of COVID-19 vaccinations, highlighting the need for further case studies to improve understanding and treatments.
  • Analysis of data from 15 patients revealed that the first vaccine dose is more likely to cause Kounis syndrome, emphasizing the importance of prompt diagnosis and monitoring for cardiac symptoms after vaccination.
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Background: Epidermal growth factor receptor () and mesenchymal-epithelial transition () gene mutations are well established in the pathogenesis of non-small cell lung cancer (NSCLC). However, there is limited understanding about the impact of rare variants, such as exon 20 insertion mutation (ex20ins) and exon 14 skipping mutation (ex14) in the Chinese population even though targeted therapies have been approved in China. We conducted a scoping review to assess the current available evidence of these two mutations in NSCLC in the Chinese population.

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Background: The treatment of spinal cord injury (SCI) is usually ineffective, because neuroinflammatory secondary injury is an important cause of the continuous development of spinal cord injury, and microglial pyroptosis is an important step of neuroinflammation. Recently, Bmal1, a core component of circadian clock genes (CCGs), has been shown to play a regulatory role in various tissues and cells. However, it is still unclear whether Bmal1 regulates microglial pyroptosis after SCI.

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Förster Resonance Energy Transfer (FRET) is a non-radiative energy transfer process in a donor-acceptor system and has applications in various fields, such as single-molecule investigations, biosensor creation, and deoxyribonucleic acid (DNA) mechanics research. The investigation of FRET processes in metal halide perovskites has also attracted great attention from the community. The review aims to provide an up-to-date study of FRET in the context of perovskite systems.

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Cellular context profiling of modification effector proteins is critical for an in-depth understanding of their biological roles in RNA -methyladenosine (mA) modification regulation and function. However, challenges still remain due to the high context complexities, which call for a versatile toolbox for accurate live-cell monitoring of effectors. Here, we propose a demethylation-switchable aptamer sensor engineered with a site-specific mA (DSA-mA) for lag-free monitoring of the mA demethylase FTO activity in living cells.

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Background: Smoking has been identified as a standalone risk factor for coronary heart disease (CHD) and myocardial infarction (MI), but the precise underlying mechanisms remain incompletely elucidated.

Results: In this study, we conducted a two-sample Mendelian randomization analysis to examine the impact of smoking behaviors (including smoking initiation, age of smoking initiation, cigarettes per day, and smoking cessation) and smoking-related DNA methylation at CpG sites on CHD and MI based on the UK Biobank dataset. Additionally, we included the FinnGen and Biobank Japan datasets as replications and performed a meta-analysis to combine the results from different data sources.

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Current therapies for toxoplasmosis rely on a few drugs, most of which have severe side effects, and seeking ideal therapies for different types of toxoplasmosis is a long-term and challenging mission. Research and development (R&D) of novel drugs against (. ) has focused on two main directions, the structural modification of lead compounds and natural products.

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Cancer is a systemic disease continuously monitored and responded to by the human global immune system. Peripheral blood immune cells, integral to this surveillance, exhibit variable phenotypes during tumor progression. Glycosylation, as one of the most prevalent and significant post-translational modifications of proteins, plays a crucial role in immune system recognition and response.

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Purpose: Pulse oximetry remote patient monitoring (RPM) post-hospital discharge increased during the COVID-19 pandemic as patients and providers sought to limit in-person encounters and provide more care in the home. However, there is limited evidence on the feasibility and appropriateness of pulse oximetry RPM in patients with cancer after hospital discharge.

Methods And Materials: This feasibility study enrolled oncology patients discharged after an unexpected admission at the Memorial Sloan Kettering Cancer Center from October 2020 to July 2021.

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  • The study explored the relationship between blood cell traits, especially neutrophils, and venous thromboembolism (VTE) using genetic data from over 173,000 individuals.
  • Researchers utilized various methods, including Mendelian randomization, to analyze genetic variants and their influence on VTE, incorporating data from a larger cohort of nearly 377,000 individuals.
  • The findings revealed that higher neutrophil counts are associated with a reduced risk of VTE, suggesting potential avenues for future prevention and treatment strategies for this condition.
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  • The study focuses on intrahepatic cholestasis of pregnancy (ICP), a liver disorder common during pregnancy, and explores its genetic causes specifically in East Asian populations compared to Europeans.
  • Researchers conducted a large genome-wide association study on serum bile acids and ICP in over 98,000 Chinese pregnancies, identifying new genetic loci linked to the disorder and its risk.
  • The findings suggest a unique genetic link to ICP in East Asians tied to historical hepatitis B epidemics, which could lead to improved detection and treatment strategies for the condition.
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  • Researchers are merging unstructured patient data with structured health records to create the MSK-CHORD dataset, consisting of varied cancer types from nearly 25,000 patients at Memorial Sloan Kettering Cancer Center.
  • This dataset allows for in-depth analysis of cancer outcomes using advanced techniques like natural language processing, revealing new relationships that smaller datasets may not show.
  • Using MSK-CHORD for machine learning models, findings suggest that incorporating features from these unstructured texts can better predict patient survival than relying solely on genomic data or cancer staging.
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Introduction: Osimertinib, the 3rd generation EGFR-TKI, has emerged as standard first-line treatment for patients with advanced EGFR mutated nonsmall cell lung cancer (NSCLC). Patients with exon 21 L858R mutation showed lower efficacy with EGFR-TKIs than those with 19Del mutation, even with osimertinib, it remains an unmet medical need to further improve the efficacy in L858R population. We present the rationale and design for FLAIR (NCT04988607), which will investigate the efficacy and safety of osimertinib plus bevacizumab versus osimertinib monotherapy in treatment-naïve recurrent or metastatic NSCLC patients harboring EGFR exon 21 L858R mutation.

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  • Non-invasive prenatal testing (NIPT) uses advanced DNA sequencing techniques to identify fetal trisomy by analyzing maternal blood samples.
  • The study introduces new methods and software to analyze large NIPT datasets, focusing on genetic variant detection, family relationships, and population structures.
  • Results show high accuracy in estimating genetic variations and allele frequencies, supporting the use of NIPT data in broader medical genetic research.
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  • Metabolites are crucial for monitoring health and therapeutic targets, yet their genetic influences during pregnancy remain largely unexplored.
  • A genome-wide association study was conducted using genetic data from 34,394 pregnant Chinese women, identifying 53 metabolite-gene associations, with 23 being new findings.
  • The research uncovered significant gene-environment interactions during pregnancy, with half of the associations showing pleiotropy and potential causal links between maternal metabolites and various human traits and diseases.
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  • The study analyzed genetic alterations in cerebrospinal fluid (CSF) from 711 patients to help classify CNS cancers and guide targeted therapies.
  • They found detectable circulating tumor DNA (ctDNA) in over half of CSF samples from patients with CNS tumors, while none was found in samples from patients without CNS tumors.
  • The research also revealed clonal evolution and resistance mechanisms over time, with ctDNA presence linked to poorer overall survival rates for these patients.
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Aims: The objective of the prospective cohort study on the incidence of metabolic diseases and risk factors in Shunde (Speed-Shunde cohort) was to evaluate the incidence of cardiovascular-kidney-metabolic (CKM) syndrome and metabolic-associated multimorbidity, such as diabetes, hypertension, dyslipidemia, and metabolic dysfunction-associated steatotic liver disease (MASLD) in Shunde, Foshan, Guangdong, China. Additionally, the study sought to identify the potential determinants that may impact the development of these conditions and the potential consequences that may result.

Methods And Result: In the Speed-Shunde cohort, data were gathered via questionnaires, physical measurements, and laboratory analyses encompassing demographic data, behavioral tendencies, anthropometric assessments, controlled attenuation parameters and liver stiffness measurement utilizing vibration-controlled transient elastography (VCTE), as well as serum and urine detection (such as oral 75g glucose tolerance tests, hemoglobin A1c levels, lipid profiles, liver and renal function tests, urinary microalbumin and creatinine levels, etc.

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  • Maintaining normal thyroid function in pregnancy is essential, as thyroid dysfunction affects a notable percentage of pregnant women, prompting a study on the genetic basis of thyroid traits among 85,421 Chinese participants.
  • The research identified 176 genetic loci linked to thyroid traits, including 125 novel associations, revealing connections between thyroid function and various health outcomes, including gestational complications and birth outcomes.
  • Findings indicate that higher levels of thyroid-stimulating hormone (TSH) during pregnancy are associated with positive metabolic effects and that thyroid-related genetics may inform future healthcare strategies for preventing disorders later in life.
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