AI Article Synopsis

  • Gallstones are linked to a higher risk of gallbladder carcinoma (GBC), but it's unclear if longer follow-up after being diagnosed with asymptomatic gallstones affects this risk.
  • In a study involving 10 GBC patients and 30 gallstone patients, researchers divided the gallstone patients into three follow-up groups to analyze their tissues.
  • RNA sequencing revealed over 1,700 differentially expressed genes related to cancer pathways, indicating that longer follow-up could increase cancer risk, especially in the groups with 1-3 years and over 10 years of follow-up.
  • GPR-87 emerged as a key gene that contributes to GBC cell proliferation and invasion, highlighting its potential as a biomarker for assessing cancer risk in gall

Article Abstract

Gallbladder stone is a major risk factor for gallbladder carcinoma (GBC), while there is still a controversy whether period of follow-up since newly diagnoses of asymptomatic gallstones increases the risk of GBC. In this study, 10 GBC patients and 30 patients with gallstones were admitted to our hospital. Patients with gallstones were divided into 3 groups according to the follow-up time, involving 10 patients with follow-up period of 1-3 years (GS3 group), 10 patients with follow-up period of 5-10 years (GS5 group), and 10 patients with follow-up period of more than 10 years (GS10 group). Tumor and para-tumor tissues of GBC patients, and gallbladder tissues of gallstone patients were collected. RNA sequencing was performed on the 50 samples. Besides, 1,704 differentially expressed genes (DEGs) were identified in tumors compared with para-tumor tissues of 10 GBC patients, which were enriched into some well-known cancer-related pathways, such as PI3K-Akt, mitogen-activated protein kinase (MAPK), Ras, and Wnt signaling pathways, and the most significant pathway was neuroactive ligand-receptor interaction. Patients with gallstones with periods of follow-up equal to 1-3 and > 10 years showed to have higher cancer risk than those with 5-10 years. and are potential biomarkers for predicting cancer risk in patients with gallstones. The results revealed that GPR-87 can promote the proliferation, migration, and invasion of GBC cells. Herein, we explored the relationship between GBC patients and patients with gallstones with different periods of follow-up in transcriptome level.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7272658PMC
http://dx.doi.org/10.3389/fonc.2020.00823DOI Listing

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