AI Article Synopsis

  • IPMNs are potentially cancerous pancreatic tumors that are often discovered by chance, requiring ongoing monitoring due to their precancerous nature.
  • New diagnostic methods are being explored to better identify high-risk IPMNs, as current imaging techniques have limitations.
  • Research comparing glycan profiles in non-invasive and invasive IPMNs reveals distinct differences that could lead to improved diagnostic options for these tumors.

Article Abstract

Intraductal papillary mucinous neoplasms (IPMNs), often found incidentally, are potentially malignant cystic tumors of the pancreas. Due to the precancerous nature, IPMNs lacking malignant features should be kept on surveillance. The follow-up relies on magnetic resonance imaging, which has a limited accuracy to define the high-risk patients. New diagnostic methods are thus needed to recognize IPMNs with malignant potential. Here, aberrantly expressed glycans constitute a promising new area of research. We compared the N-glycan profiles of non-invasive IPMN tissues (n = 10) and invasive IPMN tissues (n = 10) to those of non-neoplastic pancreatic controls (n = 5) by matrix-assisted laser desorption-ionization time-of-flight (MALDI-TOF) mass spectrometry. Both IPMN subgroups showed increased abundance of neutral composition H4N4 and decrease in H3N5F1, increase in sialylation, and decrease in sulfation, as compared to the controls. Furthermore, invasive IPMN showed an increase in terminal N-acetylhexosamine containing structure H4N5, and increase in acidic complex-type glycans, but decrease in their complex fucosylation and sulfation, as compared to the controls. In conclusion, the N-glycan profiles differed between healthy pancreatic tissue and non-invasive and invasive IPMNs. The unique glycans expressed in invasive IPMNs may offer interesting new options for diagnostics.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425445PMC
http://dx.doi.org/10.1038/s41598-023-39220-4DOI Listing

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