AQP5 Variants Affect Tumoral Expression of AQP5 and Survival in Patients with Early Breast Cancer

Soo Jung Lee, Byung Woog Kang, Jong Gwang Kim, Jin Hyang Jung, Jeeyeon Lee, Wan Wook Kim, Ho Yong Park, Jae Hwan Jeong, Ji Yun Jeong, Ji Young Park, Jae Hyung Park, Yee Soo Chae

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Background: Our previous study showed the association of AQP5 upregulation with cancer proliferation and migration in breast cancer cell lines and with unfavorable prognosis in patients with early breast cancer (EBC). In the current study, we analyzed the association of AQP5 variants or their haplotypes with AQP5 expression and their prognostic impact for survival in patients with EBC. Methods: Three AQP5 polymorphisms (rs74091166, rs3736309, and rs1964676) were selected based on the SNP database and genotyped using the Sequenom MassARRAY in 374 out of 447 patients with EBC in whom AQP5 expression had been investigated in our previous study. Results: The allele frequencies of the selected variants in the current study were similar to those from Asian data previously reported. In a univariate analysis, both rs74091166 and rs1964676 were statistically associated with survival as a dominant model of minor allele. Moreover, a multivariate survival analysis revealed that the CC genotype of rs1964676 is an independent prognostic marker of survival in EBC patients, regardless of stage, tumor subtype, and adjuvant treatment [hazard ratio = 0.399, 0.384, and 0.205; p = 0.021, 0.027, and 0.016 for disease-free survival (DFS), distant DFS, and disease-specific survival, respectively]. In particular, the CT/TT genotype of rs1964676 showed an association with strong expression of AQP5 (58.6 vs. 26.0%; p = 0.001), without any associations with clinical or pathological characteristics including tumor subtype, stage, or histologic grade. Conclusion: The current study suggests AQP5 rs1964676 as a new potential prognostic marker in patients with EBC involved in AQP5 expression.

Original languageEnglish
Pages (from-to)153-160
Number of pages8
JournalOncology
Volume92
Issue number3
DOIs
StatePublished - 1 Feb 2017

Keywords

  • Aquaporin 5
  • Early breast cancer
  • Polymorphism
  • Prognosis

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