Publications by authors named "Ya-Ning He"

Article Synopsis
  • - Polybrominated diphenyl ethers (PBDEs), particularly BDE-47, are harmful pollutants that negatively affect the human immune system, as evidenced by their toxic effects on mouse macrophage cells (RAW264.7).
  • - Exposure to BDE-47 results in reduced cell viability, increased apoptosis (cell death), and disturbances in mitochondrial function, indicating that it triggers cell death through the mitochondrial pathway.
  • - The study highlights that BDE-47 boosts oxidative stress within the cells, impairing immune function; however, treating with the antioxidant NAC can reverse these effects, while the ROS-inducer BSO worsens them.
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Background: Cancer stem cells (CSCs) are the cause of cancer recurrence because they are resistant to conventional therapy and contribute to cancer growth and metastasis. Endocrinotherapy is the most common breast cancer therapy and acquired tamoxifen (TAM) resistance is the main reason for endocrinotherapy failure during such therapy. Although acquired resistance to endocrine treatment has been extensively studied, the underlying mechanisms are unclear.

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Article Synopsis
  • This study aimed to investigate the role of the gene CXCR4 in breast cancer bone metastasis using high-flux gene chip screening.
  • The results showed that out of 396 genes analyzed, CXCR4 was significantly up-regulated in tissues with bone metastasis compared to those without, indicating its crucial involvement in this process.
  • The findings suggest that bioinformatics analysis of CXCR4 could help in understanding, diagnosing, and developing targeted gene therapies for breast cancer bone metastasis, as well as predicting patient prognosis.
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Article Synopsis
  • * Results show that as glucose concentration increases (from 5.5 to 25 mmol/L), the number of invasive cancer cells also rises significantly, along with increased expression of certain proteins (MMP-9/MMP-2) and decreased expression of E-cadherin.
  • * The findings suggest that high glucose levels enhance the invasiveness of breast cancer cells by altering the expression of key proteins involved in cell movement and adhesion.
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Background And Aims: To investigate the expression of Egfl7 in normal adult human tissues and human epithelial tumors.


Methods: RT-PCR and Western blot were employed to detect Egfl7 expression in normal adult human tissues and 10 human epithelial tumors including hepatocellular carcinoma (HCC), lung cancer, breast cancer, prostate cancer, colorectal cancer, gastric cancer, esophageal cancer, malignant glioma, ovarian cancer and renal cancer. Immunohistochemistry and cytoimmunofluorescence were subsequently used to determine the localization of Egfl7 in human epithelial tumor tissues and cell lines.

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