Tafazzin protein expression is associated with tumorigenesis and radiation response in rectal cancer: a study of Swedish clinical trial on preoperative radiotherapy

PLoS One. 2014 May 23;9(5):e98317. doi: 10.1371/journal.pone.0098317. eCollection 2014.

Abstract

Background: Tafazzin (TAZ), a transmembrane protein contributes in mitochondrial structural and functional modifications through cardiolipin remodeling. TAZ mutations are associated with several diseases, but studies on the role of TAZ protein in carcinogenesis and radiotherapy (RT) response is lacking. Therefore we investigated the TAZ expression in rectal cancer, and its correlation with RT, clinicopathological and biological variables in the patients participating in a clinical trial of preoperative RT.

Methods: 140 rectal cancer patients were included in this study, of which 65 received RT before surgery and the rest underwent surgery alone. TAZ expression was determined by immunohistochemistry in primary cancer, distant, adjacent normal mucosa and lymph node metastasis. In-silico protein-protein interaction analysis was performed to study the predictive functional interaction of TAZ with other oncoproteins.

Results: TAZ showed stronger expression in primary cancer and lymph node metastasis compared to distant or adjacent normal mucosa in both non-RT and RT patients. Strong TAZ expression was significantly higher in stages I-III and non-mucinious cancer of non-RT patients. In RT patients, strong TAZ expression in biopsy was related to distant recurrence, independent of gender, age, stages and grade (p = 0.043, HR, 6.160, 95% CI, 1.063-35.704). In silico protein-protein interaction study demonstrated that TAZ was positively related to oncoproteins, Livin, MAC30 and FXYD-3.

Conclusions: Strong expression of TAZ protein seems to be related to rectal cancer development and RT response, it can be a predictive biomarker of distant recurrence in patients with preoperative RT.

Publication types

  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyltransferases
  • Adaptor Proteins, Signal Transducing / biosynthesis
  • Adult
  • Aged
  • Biomarkers, Tumor / biosynthesis*
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Humans
  • Immunohistochemistry
  • Inhibitor of Apoptosis Proteins / biosynthesis
  • Lymphatic Metastasis
  • Male
  • Membrane Proteins / biosynthesis
  • Middle Aged
  • Neoplasm Proteins / biosynthesis
  • Neoplasm Staging
  • Rectal Neoplasms / pathology
  • Rectal Neoplasms / radiotherapy*
  • Transcription Factors / biosynthesis*

Substances

  • Adaptor Proteins, Signal Transducing
  • BIRC7 protein, human
  • Biomarkers, Tumor
  • FXYD3 protein, human
  • Inhibitor of Apoptosis Proteins
  • Membrane Proteins
  • Neoplasm Proteins
  • TMEM97 protein, human
  • Transcription Factors
  • Acyltransferases
  • TAFAZZIN protein, human

Grants and funding

This study was financially supported by grants from the Swedish Cancer Foundation, Swedish Research Council and the Health Research Council in the South-East of Sweden. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.