AI Article Synopsis

  • - Linc-pint, a long noncoding RNA, is found to be involved in regulating tumor cell growth in pancreatic cancer (PCa) patients, with its expression levels assessed through qRT-PCR and RNA FISH techniques.
  • - The study shows that Linc-pint levels are lower in the plasma of PCa patients compared to healthy individuals, suggesting it may be a more sensitive biomarker for detecting PCa than the traditional CA19-9 marker.
  • - Additionally, decreased Linc-pint levels in both plasma and tumor tissues are linked to tumor recurrence and poor prognosis, indicating its potential role as a minimally invasive biomarker for early detection and prognosis in PCa patients.

Article Abstract

Long intergenic non-protein coding RNA, p53 induced transcript (Linc-pint) is a long noncoding RNA (lncRNA) that regulates tumor cell viability and proliferation. We used qRT-PCR and RNA FISH analysis to evaluate Linc-pint levels in the plasma and tumor tissues of pancreatic cancer (PCa) patients. Our data demonstrate that Linc-pint expression is lower in plasma samples from PCa patients than from healthy individuals, and indicate that plasma Linc-pint levels are more sensitive than CA19-9 for detecting PCa. Our data also show that Linc-pint levels are lower in PCa tumors than in adjacent tissues, carcinoma of the ampulla of Vater (CAV) and cholangiocarcinoma (CCA), and suggest that Linc-pint could be used for distinguishing the cause of malignant obstructive jaundice. Low plasma Linc-pint levels correlate with tumor recurrence, while low tumor Linc-pint levels correlate with poor prognosis for PCa patients after pancreatectomy. These results thus indicate that low plasma Linc-pint expression could serve as a minimally invasive biomarker for early PCa detection, and that low Linc-pint levels in PCa tumors could be used for predicting patient prognosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342121PMC
http://dx.doi.org/10.18632/oncotarget.12365DOI Listing

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