Tubulin detyrosination is a frequent occurrence in breast cancers of poor prognosis

A Mialhe1, L Lafanechère, I Treilleux

  • 1Laboratoire du Cytosquelette, Institut National de la Santé et de la Recherche Médicale (INSERM) U366, Département de Biologie Molèeculaire et Structurale, Commissariat á l'Energie Atomique, 38054 Grenoble Cedex 9, France.

Cancer Research
|June 30, 2001
PubMed

Insights

Detyrosinated tubulin, a modified form of a key cell protein, accumulates in aggressive breast cancers. This finding, linked to tumor aggressiveness, may help identify high-risk patients.

Area of Science:

  • Cell Biology
  • Oncology
  • Biochemistry

Background:

  • Tubulin, a major cell protein, is crucial for cell division and undergoes posttranslational modifications.
  • Detyrosinated tubulin accumulates in cancer cells, suggesting a role in tumor progression.
  • Previous studies indicated tubulin detyrosination provides a selective advantage to cancer cells.

Purpose of the Study:

  • To investigate the occurrence and significance of tubulin detyrosination in human breast tumors.
  • To correlate tubulin detyrosination with tumor aggressiveness and patient outcomes.

Main Methods:

  • Immunohistochemical staining of paraffin-embedded breast tumor sections from 134 patients.
  • Analysis of tubulin detyrosination in relation to Scarf-Bloom-Richardson (SBR) grade and mitotic score.
  • Correlation of detyrosination index with clinical outcome and patient follow-up data.

Main Results:

  • Tubulin detyrosination was observed in 53% of breast tumors, predominantly in 19.4%.
  • Detyrosination significantly correlated with higher SBR grade (P < 0.001), particularly the mitotic score.
  • While SBR grade and detyrosination index alone lacked prognostic value, a combined index showed significance (P = 0.02).

Conclusions:

  • Tubulin detyrosination is a frequent and easily detectable marker in breast cancer.
  • It is significantly linked to tumor aggressiveness, especially in higher SBR grades.
  • Further research may establish tubulin detyrosination as a prognostic tool, particularly in SBR grade 2 tumors.

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