Is vimentin a potential prognostic factor for patients with triple-negative breast cancer?

J Cancer Res Clin Oncol. 2020 Aug;146(8):2109-2116. doi: 10.1007/s00432-020-03210-0. Epub 2020 Apr 7.

Abstract

Objective: To evaluate the prognostic potential of vimentin, p53, EGFR, CK5/6, CK 14, and CK 17 in patients with triple-negative breast cancer (TNBC).

Material and methods: Tumor specimens of 60 patients with histologically confirmed TNBC were retrospectively analyzed. Formalin-fixed paraffin-embedded blocks of the tumor tissue were used to prepare tissue microarrays (TMAs). After immune-histochemical staining, protein expression of vimentin, p53, EGFR, CK5/6, CK 14, and CK 17 was determined and the immunoreactive score (IRS) was calculated. The protein expression was correlated to overall (OS) and disease-free survival (DFS).

Results: Ninety percent of patients suffered from an invasive ductal carcinoma T1 or T2, 66.7% were N0, and 70% had a G3 tumor with Ki67 of > 14%. Vimentin expression was found in 28/60 patients (46.7%), p53 expression in 30/60 patients (50%), and EGFR expression in 3/60 patients (5%). CK5/6, CK14, and CK17 expression was found in 60.0%, 63.3%, and 66.7%, respectively. Vimentin expression vs no expression was associated with significantly higher mean Ki67 values (52.5% vs. 31.1%; p = 0.0013) and significantly higher p53 expression (67.9% vs. 34.4%; p = 0.0097). No significant association between vimentin expression and OS (p = 0.7710) or DFS (p = 0.5558) was found during a mean follow-up of 92 months.

Conclusion: None of the six proteins proved to be suitable prognostic factors for OS and DSF in patients with TNBC.

Keywords: Cytokines; EGFR; Triple-negative breast cancer; Vimentin; p53.

MeSH terms

  • Biomarkers, Tumor / biosynthesis
  • Female
  • Humans
  • Immunohistochemistry
  • Neoplasm Staging
  • Prognosis
  • Retrospective Studies
  • Tissue Array Analysis
  • Triple Negative Breast Neoplasms / metabolism*
  • Triple Negative Breast Neoplasms / pathology
  • Vimentin / biosynthesis*

Substances

  • Biomarkers, Tumor
  • VIM protein, human
  • Vimentin