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Pseudobudding: ruptured glands do not represent true tumor buds.

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Tumor budding (TB) indicates poor prognosis in cancers. This study differentiates true TB from pseudobudding (PsB), finding TB shows active invasion while PsB is a reactive inflammatory response, advising against assessing TB in inflamed areas.

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colorectal cancerimmunohistochemistrymultiplex immunofluorescencepseudobuddingspatial transcriptomicstransmission electron microscopytumor budding

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Area of Science:

  • Oncology
  • Pathology
  • Cancer Biology

Background:

  • Tumor budding (TB) is a critical prognostic biomarker in colorectal and other solid cancers, defined as single cancer cells or small clusters at the invasive front.
  • Pseudobudding (PsB) can mimic TB in areas of inflammation and glandular disruption, posing a diagnostic challenge.

Purpose of the Study:

  • To elucidate the distinct biological characteristics of tumor budding (TB) and pseudobudding (PsB).
  • To provide guidance on differentiating TB from PsB in routine cancer diagnostics.

Main Methods:

  • Utilized orthogonal approaches to analyze cellular and microenvironmental features of TB and PsB.
  • Examined markers of epithelial-mesenchymal transition (EMT) and extracellular matrix (ECM) deposition.
  • Assessed the presence and type of inflammatory cells within the tumor microenvironment (TME).

Main Results:

  • Tumor budding (TB) exhibits features of active invasion, including epithelial-mesenchymal transition (EMT) markers.
  • TB is associated with increased extracellular matrix (ECM) deposition in the surrounding tumor microenvironment (TME).
  • Pseudobudding (PsB) is linked to a reactive inflammatory response, characterized by increased granulocytes in the TME.

Conclusions:

  • Clear biological differences exist between tumor budding (TB) and pseudobudding (PsB).
  • TB reflects active tumor invasion, whereas PsB is a response to inflammation.
  • Diagnostic assessment of TB should avoid areas with significant inflammatory reactions to ensure accuracy.