Publications by authors named "Tianyu Qu"

The dysregulation of N6-methyladenosine (m6A) RNA modification is widely recognized for its crucial roles in various diseases, including pulmonary hypertension (PH). Prior studies have highlighted the significant role of methyltransferase-like 3 (METTL3) in the pathogenesis of PH. Nevertheless, the potential and underlying mechanisms of METTL3 and its inhibitors as targets for PH treatment require further elucidation.

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Background: Extrachromosomal circular DNAs (eccDNAs) have been reported to play a key role in the occurrence and development of various diseases. However, the characterization and role of eccDNAs in pulmonary arterial hypertension (PAH) remain unclear.

Methods: In the discovery cohort, we first explored eccDNA expression profiles by Circle-sequencing analysis.

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Article Synopsis
  • - Researchers found that lung cancer patients with EGFR mutations benefit from EGFR-TKI treatments, but resistance to these drugs develops over time, making it crucial to understand the underlying molecular mechanisms of this resistance.
  • - The study identified LINC00969, a long non-coding RNA (lncRNA), which is overexpressed in lung cancer cells that have become resistant to the drug gefitinib, and it plays a role in regulating that resistance through various molecular interactions.
  • - LINC00969 inhibits the expression of NLRP3, a protein involved in a specific cell death pathway (pyroptosis), by modifying certain chemical signals on DNA and RNA, suggesting it could be a new biomarker and therapeutic target for
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Acquired resistance to epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKI, such as gefitinib) in lung cancer continues to be a major problem. Recent studies have shown the promise of ferroptosis-inducing therapy in EGFR-TKI resistant cancer, but have not been translated into clinical benefits. Here, we identified carbonic anhydrase IX (CA9) was upregulated in gefitinib-resistant lung cancer.

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Background: The combination of antiangiogenic agents with epidermal growth factor receptor inhibitors (EGFR-TKIs) and chemotherapy with EGFR-TKIs are the most common combination treatment options in epidermal growth factor receptor (EGFR) positive non-small cell lung cancer (NSCLC). This network meta-analysis was performed to evaluate the differences between them.

Methods: We searched the PubMed, EMBASE and the Cochrane Controlled Trials Register up to August 2022.

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Article Synopsis
  • c-Myc and E2F1 are crucial in many cancers, and long noncoding RNAs (lncRNAs) like MNX1-AS1 can influence tumor-related processes in their regulation.
  • The study found that MNX1-AS1 is increased in non-small cell lung cancer (NSCLC) due to c-Myc activation and is linked to worse patient outcomes by enhancing cell growth and tumor formation.
  • MNX1-AS1 interacts with IGF2BP1, stabilizing c-Myc and E2F1 mRNA, leading to a feedback loop that accelerates cell proliferation, suggesting potential for MNX1-AS1 as a biomarker and therapeutic target in NSCLC.
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Article Synopsis
  • Long non-coding RNAs (lncRNAs), particularly MELTF-AS1, are crucial in the development of non-small cell lung cancer (NSCLC) and are linked to poor patient outcomes.
  • MELTF-AS1 is found to enhance tumor growth and spread by regulating cell functions, with its expression increased through copy number amplification and transcription factor SP1 activation.
  • The study highlights how MELTF-AS1 interacts with the RNA-binding protein YBX1 to promote transcription of the gene ANXA8, suggesting new avenues for diagnostics and treatments in NSCLC.
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Bone defects occurring for various reasons can lead to deformities and dysfunctions of the human body. Considering the need for clinical applications, it is essential for bone regeneration to exploit a scaffold with bioactive bone cement. In this study, we fabricated bioactive magnesium phosphate bone cement (BMPC) at room temperature; then, it was set at to °C and 100% humidity for 2 h.

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Background: Coronavirus disease 2019 (COVID-19) has rapidly spread worldwide. Systematic analysis of lung cancer survivors at molecular and clinical levels is warranted to understand the disease course and clinical characteristics.

Methods: A single-center, retrospective cohort study was conducted in 65 patients with COVID-19 from Wuhan Huoshenshan Hospital, of which 13 patients were diagnosed with lung cancer.

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Background: To compare the benefits and explore the cause of acquired resistance of epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) and its combination with chemotherapy in advanced non-small-cell lung cancer (NSCLC) patients harboring EGFR mutation in a real-life setting.

Methods: This retrospective analysis included 117 advanced NSCLC patients with EGFR mutation who underwent next-generation sequencing (NGS) prior to treatment. The combination group included 50 patients who received the regimen of EGFR-TKI combined with chemotherapy, while the EGFR-TKI monotherapy group included 67 patients treated with TKI only.

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Clinical research data show that gefitinib greatly improves the progression-free survival of patients, so it is used in advanced non-small cell lung cancer patients with EGFR mutation. However, some patients with EGFR sensitive mutations do not have good effects on initial gefitinib treatment, and this mechanism is rarely studied. METTL3, a part of N6-adenosine-methyltransferase, has been reported to play an important role in a variety of tumours.

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Breast cancer (BC) is a leading cause of cancer mortality in women worldwide. MAC30/Transmembrane protein 97 (TMEM97) is aberrantly up-regulated in many human carcinoma cells. However, the function of MAC30 in invasion and EMT of BC cells is uncertain.

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Neuropeptide Y (NPY) exhibits a critical but poorly understood regulatory signaling function and has been shown to promote proliferation, vascularization and migration in several types of cells and tissues. However, little is known about the specific role of NPY in the proliferation and apoptosis of bone marrow stromal cells (also known as bone marrow-derived mesenchymal stem cells, BMSCs), which contain a subpopulation of multipotent skeletal stem cells. Based on BrdU incorporation tests, Cell Counting Kit-8, flow cytometry, quantitative polymerase chain reaction and western blotting, we showed that NPY significantly promoted the proliferation of BMSCs in a concentration-dependent manner, with a maximal effect observed at a concentration of 10M for pro-proliferative and 10M for anti-apoptotic activities.

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