Publications by authors named "Xiang-Qi Chen"

Article Synopsis
  • Gastric cancer (GC) is a serious illness, and a certain protein (non-SMC condensin II complex subunit D3) is linked to it but hasn't been studied much before.
  • Researchers looked at data from cancer patients and lab tests to understand how this protein affects GC and found that higher levels of this protein are connected to worse health outcomes.
  • They discovered that reducing this protein can help slow down the growth of cancer cells and might be a good target for new treatments.
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  • A study was conducted to analyze the clinical features and outcomes of advanced neuroendocrine carcinomas (NECs), focusing on small-cell lung cancer (SCLC), to improve treatment approaches.
  • Data from 123 patients with both intra-pulmonary (IPNECs) and extra-pulmonary neuroendocrine carcinomas (EPNECs) were reviewed, revealing that IPNECs had a longer median overall survival compared to EPNECs.
  • Key factors impacting patient survival included age, liver metastasis, the number of chemotherapy cycles, and chest radiotherapy, highlighting the importance of comprehensive treatment strategies like multi-cycle chemotherapy and combined therapies for better outcomes.
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Serum miRNAs are available clinical samples for cancer screening. Identifying early serum markers in lung cancer (LC) is essential for patients' early diagnosis and clinical treatment. Expression data of serum miRNAs of lung adenocarcinoma (LUAD) patients and healthy individuals were downloaded from the Gene Expression Omnibus (GEO).

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Background: Combined hepatocellular-cholangiocarcinoma (cHCC-CCA) is a form of rare primary liver cancer that combines intrahepatic cholangiocarcinoma (ICC) and hepatocellular carcinoma.

Aim: To investigate overall survival (OS) and recurrence-free survival (RFS) after radical resection in patients with cHCC-CCA, and the clinicopathological factors affecting prognosis in two center hospitals of China.

Methods: We reviewed consecutive patients with cHCC-CCA who received radical resection between January 2005 and September 2021 at Peking Union Medical College and the 5th Medical Center of the PLA General Hospital retrospectively.

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Background: Rho GTPase activating protein 10 (ARHGAP10) has been implicated as an essential element in multiple cellular process, including cell migration, adhesion and actin cytoskeleton dynamic reorganization. However, the correlation of ARHGAP10 expression with epithelial-mesenchymal transition (EMT) in lung cancer cells is unclear and remains to be elucidated. Herein, we investigated the relationship between the trait of ARHGAP10 and non-small cell lung cancer (NSCLC) pathological process.

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Background: Immune checkpoint inhibitors (ICIs) have been identified as validated medications in non-small cell lung cancer (NSCLC). However, they are often associated with immune-related adverse events (irAEs) including liver dysfunction. Therefore, we conducted a systematic review of the literature and performed a meta-analysis to ascertain overall incidence and risk of immune mediated liver dysfunction in NSCLC patients.

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Background: The programmed cell death-1 (PD-1)/programmed cell death ligand-1 (PD-L1) inhibitors have shown encouraging merits in non-small cell lung cancer (NSCLC) patients, however, they are often related to potentially fatal immune-related adverse events (irAEs) including colitis. Considering the incidence and characteristics of immune-related colitis may have significant implications for the appropriate utilization of PD-1/PD-L1 inhibitors in clinical practice, we conduct this meta to systematically analyze the correlation between PD-1/PD-L1 inhibitors for the treatment of NSCLC and the incidence of immune-associated colitis.

Methods: Electronic databases including PubMed, Embase, Cochrane Library and ClinicalTrials.

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Objective To investigate the expression and clinicopathological significance of the oestrogen receptor (ER) in non-small cell lung cancer (NSCLC). Methods ER expression was examined by immunohistochemical staining of tumour tissue and adjacent normal lung tissue from 67 NSCLC patients. The relationships between ER expression and clinicopathological features were analysed.

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Article Synopsis
  • The study investigated the impact of sorafenib on the growth, death (apoptosis), and invasion of cisplatin-resistant A549 lung cancer cells in lab conditions.
  • Sorafenib was tested at four different concentrations (2, 4, 8, and 16 µmol/l) over 24, 48, and 72 hours, with significant inhibition of cell growth observed at all concentrations.
  • Results showed that sorafenib not only increased the rates of apoptosis in the cancer cells but also significantly reduced their invasion capabilities, suggesting its potential effectiveness in treating resistant lung adenocarcinoma.
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The aim of this study was to investigate whether the modification of bone marrow-derived mesenchymal stem cells (BMSCs) with the fused FGF4 (fibroblast growth factor 4)-bFGF (basic fibroblast growth factor) gene could improve the expression and secretion of BFGF, and increase the efficacies in repairing infarcted myocardium. We used In-Fusion technique to construct recombinant lentiviral vectors containing the individual gene of bFGF, enhanced green fluorescent protein (EGFP), or genes of FGF4-bFGF and EGFP, and then transfected these lentiviruses into rat BMSCs. We conducted an in vitro experiment to compare the secretion of bFGF in BMSCs infected by these lentiviruses and also examined their therapeutic effects in the treatment of myocardial infraction in a rodent study.

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  • The study investigated the role of survivin in human lung cancer, confirming its high expression in A549 lung cancer cells through immunohistochemistry.
  • The researchers used RNA interference (RNAi) to effectively downregulate survivin expression in these cells, verified by quantitative PCR and western blotting.
  • Results indicated that lowering survivin levels significantly reduced cancer cell proliferation, invasion, and migration, highlighting its importance in lung cancer development.
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The survivin protein, a member of the inhibitors of apoptosis (IAP) family, has gained popularity as a therapeutic target for cancer due to its selective expression in tumor cells and its significant involvement in tumor cell viability. The aim of this study was to investigate the effect of the survivin-small interfering RNA (siRNA) plasmid on survivin expression in the human lung cancer cell line, A549, and to observe its effects on apoptosis and proliferation of A549 cells. A549 human lung cancer cells were transfected with survivin-targeting siRNA.

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Objective: To investigate the effects of Interleukin-18 (IL-18) on asthmatic airway inflammation.

Methods: Thirty healthy adult male guinea pigs were randomly divided into 3 equal groups: asthmatic model group (Group A, undergoing intraperitoneally injection of ovalbumin (OVA) once and spraying of OVA aerosol once a day for 5 days; control group (Group B), undergoing intraperitoneally injection of OVA once and spraying of normal saline aerosol once a day for 5 days; and interleukin (IL)-18 intervention group (Group C, undergoing intraperitoneally injection of OVA once and intraperitoneal injection of IL-18 on the days 1, 3, 8. 10.

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