Publications by authors named "Tiansheng Xu"

Article Synopsis
  • Papillary thyroid cancer (PTC) is increasing in incidence, and this study investigates the role of TM4SF4 in its progression, finding it significantly upregulated in PTC cases.
  • TM4SF4 is identified as a potential diagnostic marker for PTC, with analyses indicating its involvement in cell junctions and immune activation related to the disease.
  • Experimental results show that reducing TM4SF4 levels decreases cell growth and spread of PTC, while reactivating the AKT pathway can reverse these effects, underscoring TM4SF4's role in promoting PTC progression.
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This study examined the spoilage potential of specific spoilage organisms on the degradation of adenosine triphosphate (ATP)-related compounds in vacuum-packed refrigerated large yellow croaker. The total viable count (TVC), ATP-related compounds and related enzymes of vacuum-packed refrigerated large yellow croaker inoculated with different bacteria ( and ) were characterized using the spread plate method, high-performance liquid chromatography and assay kits, respectively. Results indicated that the TVC for both control and groups reached spoilage levels at days 9 and 15, respectively.

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Background: A few studies have reported the distribution of the microbiota in breast cancer tissues, but few reports have compared the microbiota in different subtypes of breast cancer tissue. Moreover, no study has reported on the relationship between the microbiota and gene expression in breast tumor.

Methods: Sections of formalin-fixed paraffin-embedded (FFPE) tissue were prepared from the breast tumors of 70 patients and were subjected to microarray analysis to identify gene expression profiles.

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Medullary thyroid carcinoma (MTC) is a rare neuroendocrine malignancy derived from parafollicular cells (C cells) of the thyroid. Here we presented a comprehensive multi-omics landscape of 102 MTCs through whole-exome sequencing, RNA sequencing, DNA methylation array, proteomic and phosphoproteomic profiling. Integrated analyses identified BRAF and NF1 as novel driver genes in addition to the well-characterized RET and RAS proto-oncogenes.

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