Protocol for region-specific tumor dissection and protein extraction from a pancreatic neuroendocrine tumor mouse

Vinod Vijayakurup1, Michael Feely2, Maria Zajac-Kaye1

  • 1Department of Anatomy and Cell Biology, University of Florida, Gainesville, FL 32610, USA.

STAR Protocols
|June 19, 2026
PubMed

Insights

This study presents a protocol for isolating high-quality protein from mouse pancreatic neuroendocrine tumors. The method ensures protein integrity and enhances extract specificity for better tumor mechanism research.

Area of Science:

  • Oncology
  • Molecular Biology
  • Biochemistry

Background:

  • High-quality protein isolation is crucial for understanding tumor development mechanisms.
  • Transgenic mouse models, such as human thymidylate synthase (hTS)/Men1 knockout (Men1-/-) mice, are vital for studying specific genetic contributions to cancer.
  • Pancreatic neuroendocrine tumors (PNETs) present unique challenges for protein extraction due to tissue complexity.

Purpose of the Study:

  • To describe a detailed protocol for harvesting and extracting protein from hTS/Men1-/- and control Men1-/- mouse pancreatic tumors.
  • To optimize protein extraction for immunoblotting applications.
  • To enhance the specificity and integrity of protein extracts from challenging pancreatic tissues.

Main Methods:

  • Harvesting of pancreatic neuroendocrine tumors from hTS/Men1-/- and control Men1-/- mice.
  • Detailed protein extraction procedures specifically adapted for pancreatic tumor tissues.
  • Methods to minimize non-tumor tissue contamination and reduce non-specific background.

Main Results:

  • The described protocol successfully yields high-quality protein extracts from mouse pancreatic neuroendocrine tumors.
  • Protein integrity is preserved during the extraction process.
  • Non-specific background commonly observed in pancreatic tissue extracts is significantly reduced, enhancing specificity.

Conclusions:

  • This protocol provides a reliable method for obtaining pure protein extracts from hTS/Men1-/- mouse tumors.
  • The optimized method facilitates accurate immunoblotting and downstream analyses for studying tumor development.
  • The protocol is essential for researchers investigating the role of hTS/TYMS overexpression in a Men1-/- background.

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