CytoLyt fixation impedes insulinoma-associated protein 1 (INSM1) immunoreactivity compared to formalin fixation

Michelle Garlin-Politis1, Swikrity Upadhyay Baskota2, Sarah Picon1

  • 1Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York Presbyterian Hospital, New York, New York.

Insights

Insulinoma-associated protein 1 (INSM1) staining is significantly reduced in CytoLyt-fixed cell blocks compared to formalin-fixed specimens, potentially leading to false negatives in neuroendocrine tumor diagnoses.

Area of Science:

  • Pathology
  • Oncology
  • Immunohistochemistry

Background:

  • Insulinoma-associated protein 1 (INSM1) is a key immunohistochemical marker for neuroendocrine tumors/carcinomas (NETs/NECs).
  • Previous studies suggested INSM1 exhibits comparable staining in both CytoLyt-fixed cell blocks and formalin-fixed tissues.
  • This study investigates INSM1 expression variability between these two fixation methods.

Purpose of the Study:

  • To compare INSM1 immunoreactivity in CytoLyt-fixed versus formalin-fixed cell blocks from NET/NEC cases.
  • To identify factors influencing potential discrepancies in INSM1 staining between fixation methods.

Main Methods:

  • Retrospective analysis of 20 NET/NEC cases with both formalin- and CytoLyt-fixed cell blocks.
  • Evaluation of INSM1 staining (positive, negative, equivocal) in both fixation types.
  • Detailed scoring of equivocal staining by percentage and intensity.

Main Results:

  • All formalin-fixed cell blocks showed widespread INSM1 positivity (>90%).
  • CytoLyt-fixed cells demonstrated negative INSM1 staining in 65% of cases.
  • 30% of CytoLyt-fixed samples showed equivocal INSM1 positivity.

Conclusions:

  • INSM1 immunohistochemical staining is significantly reduced in CytoLyt-fixed cell blocks compared to formalin-fixed specimens.
  • Reduced INSM1 staining in CytoLyt-fixed material can lead to false-negative results.
  • This finding highlights a potential diagnostic pitfall for NET/NEC when using CytoLyt-fixed cell blocks.
Abstract