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NAA10 gene expression is associated with mesenchymal transition, dedifferentiation, and progression of clear cell renal cell carcinoma.
Duong, Nguyen Xuong; Nguyen, Thao; Le, Minh-Khang; Sawada, Norifumi; Kira, Satoru; Kondo, Tetsuo; Inukai, Takeshi; Mitsui, Takahiko.
Affiliation
  • Duong NX; Department of Urology, University of Yamanashi Graduate School of Medical Sciences, Chuo-city 409-3898, Japan; Department of Urology, Cho Ray Hospital, Ho Chi Minh city, Vietnam. Electronic address: dr.duongnguyenxuong@gmail.com.
  • Nguyen T; Department of Pediatrics, University of Yamanashi Graduate School of Medical Sciences, Chuo-city 409-3898, Japan. Electronic address: nthao.med@gmail.com.
  • Le MK; Department of Human Pathology, University of Yamanashi Graduate School of Medical Sciences, Chuo-city 409-3898, Japan. Electronic address: g20ddm26@yamanashi.ac.jp.
  • Sawada N; Department of Urology, University of Yamanashi Graduate School of Medical Sciences, Chuo-city 409-3898, Japan. Electronic address: nsawada@yamanashi.ac.jp.
  • Kira S; Department of Urology, University of Yamanashi Graduate School of Medical Sciences, Chuo-city 409-3898, Japan. Electronic address: skira@yamanashi.ac.jp.
  • Kondo T; Department of Human Pathology, University of Yamanashi Graduate School of Medical Sciences, Chuo-city 409-3898, Japan. Electronic address: ktetsuo@yamanashi.ac.jp.
  • Inukai T; Department of Pediatrics, University of Yamanashi Graduate School of Medical Sciences, Chuo-city 409-3898, Japan. Electronic address: tinukai@yamanashi.ac.jp.
  • Mitsui T; Department of Urology, University of Yamanashi Graduate School of Medical Sciences, Chuo-city 409-3898, Japan. Electronic address: tmitsui@yamanashi.ac.jp.
Pathol Res Pract ; 255: 155191, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38340582
ABSTRACT

INTRODUCTION:

We aimed to investigate the expression and prognostic role of NAA10 in clear cell renal cell carcinoma (ccRCC). MATERIAL AND

METHODS:

We performed a gene expression and survival analysis based on the human cancer genome atlas database of ccRCC patients (TCGA-KIRC).

RESULTS:

The patients in the TCGA-KIRC (n = 537) were divided into two subgroups NAA10-low and NAA10-high expression groups. NAA10-high ccRCC exhibited higher T stages (p = 0.002), a higher frequency of distant metastasis (p = 0.018), more advanced AJCC stages (p < 0.001), a lower overall survival time (p = 0.036), and a lower survival rate (p < 0.001). NAA10-high ccRCC was associated with increased activity of non-specific oncogenic pathways, including oxidative phosphorylation (p < 0.001) and cell cycle progression [G2 to M phase transition (p = 0.045) and E2F targets (p < 0.001)]. Additionally, the NAA10-high tumors showed reduced apoptosis via TRIAL pathways (p < 0.001) and increased levels of activity that promoted epithelial-mesenchymal transition (p = 0.026) or undifferentiation (p = 0.01). In ccRCC, NAA10 expression was found to be a negative prognostic factor in both non-metastatic (p < 0.001) and metastatic tumors (p = 0.032).

CONCLUSIONS:

In ccRCC, NAA10 expression was shown to be a negative prognostic factor related to tumor progression rather than tumor initiation, and high NAA10 expression promoted epithelial-mesenchymal transition and undifferentiation.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Renal Cell / Kidney Neoplasms Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Pathol Res Pract Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Carcinoma, Renal Cell / Kidney Neoplasms Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Pathol Res Pract Year: 2024 Document type: Article