Publications by authors named "Bo-Shih Huang"

r () infection affects cell survival pathways, including apoptosis and proliferation in host cells, and disruption of this balance is the key event in the development of -induced gastric cancer (HPGC). infection induces alterations in microRNAs expression that may be involved in GC development. Bioinformatic analysis showed that microRNA-21 (miR-21) is significantly upregulated in HPGC.

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Hepatocellular carcinoma is one of the most common cancer types worldwide. In cases of advanced-stage disease, sorafenib is considered the treatment of choice. However, resistance to sorafenib remains a major obstacle for effective clinical application.

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Background: Pancreatic cancer-associated diabetes mellitus (PCDM) is a paraneoplastic phenomenon characterized by worsening hyperglycaemia and weight loss. Galectin-3 and S100A9, mediators of PCDM, have pro-inflammatory functions and might thereby induce systemic inflammation and cachexia. We aimed to examine whether PCDM directly mediates cachexia.

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Objective: Pancreatic cancer-associated diabetes (PCDM) is a paraneoplastic phenomenon accounting for 1% of new-onset diabetes. We aimed to identify the mediators of PCDM and evaluate their usefulness in distinguishing PCDM from type 2 diabetes.

Research Design And Methods: Secreted proteins of MIA PaCa-2 cells were identified by proteomics, and those with ≥10-fold overexpression in transcriptome analysis were assessed by bioinformatics and glucose uptake assay to identify candidate factors.

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Helicobacter pylori infection is associated with the development of gastric and duodenal ulcers as well as gastric cancer. GroES of H. pylori (HpGroES) was previously identified as a gastric cancer-associated virulence factor.

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Article Synopsis
  • Helicobacter pylori (H. pylori) infection is linked with chronic gastritis, duodenal ulcers, and gastric cancer, prompting researchers to find biomarkers for gastric cancer (GC).
  • A study using iTRAQ revealed 99 proteins with higher expression in GC patients compared to those with duodenal ulcers, identifying four potential antigens—AlpA, OipA, BabA, and SabA—that are more prevalent in GC patients.
  • The combination of OipA, BabA, and SabA significantly improved the ability to differentiate between GC and non-GC patients, with a prediction accuracy of 77.3%, leading to the creation of a diagnostic protein microarray for rapid detection of H.
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