Literature DB >> 22344708

Loss of NKX3-1 as a potential marker for an increased risk of occult lymph node metastasis and poor prognosis in oral squamous cell carcinoma.

Ken Miyaguchi1, Narikazu Uzawa, Kaoru Mogushi, Ken-Ichiro Takahashi, Chieko Michikawa, Yoshimi Nakata, Jun Sumino, Norihiko Okada, Hiroshi Mizushima, Yutaka Fukuoka, Hiroshi Tanaka.   

Abstract

The prognosis of oral squamous cell carcinoma (OSCC) is significantly dependent on the existence of cervical lymph node metastasis (LNM), with the overall survival rate being much lower in patients with LNM. Primary causes and molecular mechanisms of LNM are still largely unclear. We hypothesized that factors related with cancer progress and/or prognosis in OSCC are revealed by genome-wide investigation of DNA copy number aberrations (CNAs). In order to find biomarkers for occult LNM of OSCC, we comprehensively investigated genomic DNAs from 60 OSCC patients using Affymetrix mapping arrays and statistically analyzed correlations between CNAs of genes and the presence of occult LNM in the patients. The genome-wide CNA study indicated significant correlations between the presence of occult LNM and CNAs of certain genes. Through a literature survey, we narrowed down the candidates and focused on loss of NKX3-1, which is a homeodomain-containing transcription factor. NKX3-1 is known as a tumor suppressor gene in prostate cancer but has never been reported in OSCC. Quantitative RT-PCR and immunohistochemistry (IHC) analyses also showed significantly lower expression of NKX3-1 in the cases with occult LNM, which was further validated by IHC analysis in independent cases. The survival analyses indicated that NKX3-1 loss is a significant risk factor to decrease the disease-free survival (DFS) and the overall survival (OS) rates. This is the first time that the significant association of NKX3-1 loss and occult LNM was indicated in OSCC. The present results suggest that loss of NKX3-1 may be a potential biomarker for occult LNM of OSCC.

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Year:  2012        PMID: 22344708     DOI: 10.3892/ijo.2012.1373

Source DB:  PubMed          Journal:  Int J Oncol        ISSN: 1019-6439            Impact factor:   5.650


  6 in total

1.  Genome-wide gene expression profiling of tongue squamous cell carcinoma by RNA-seq.

Authors:  Hai Xia Zhang; Ou Sheng Liu; Chao Deng; Yan He; Ye Qian Feng; Jin An Ma; Chun Hong Hu; Zhan Gui Tang
Journal:  Clin Oral Investig       Date:  2017-03-29       Impact factor: 3.573

2.  KLF5-induced miR-487a augments the progression of osteosarcoma cells by targeting NKX3-1 in vitro.

Authors:  Anyu Luo; Hanlin Liu; Chen Huang
Journal:  Oncol Lett       Date:  2022-06-14       Impact factor: 3.111

3.  NK3 homeobox 1 (NKX3.1) up-regulates forkhead box O1 expression in hepatocellular carcinoma and thereby suppresses tumor proliferation and invasion.

Authors:  Jingyi Jiang; Zheng Liu; Chao Ge; Cong Chen; Fangyu Zhao; Hong Li; Taoyang Chen; Ming Yao; Jinjun Li
Journal:  J Biol Chem       Date:  2017-09-27       Impact factor: 5.157

4.  PARVB overexpression increases cell migration capability and defines high risk for endophytic growth and metastasis in tongue squamous cell carcinoma.

Authors:  A Eslami; K Miyaguchi; K Mogushi; H Watanabe; N Okada; H Shibuya; H Mizushima; M Miura; H Tanaka
Journal:  Br J Cancer       Date:  2014-11-25       Impact factor: 7.640

5.  The Homeodomain Transcription Factor NKX3.1 Modulates Bladder Outlet Obstruction Induced Fibrosis in Mice.

Authors:  Mehul S Patel; Diana K Bowen; Nicholas M Tassone; Andrew D Gould; Kirsten S Kochan; Paula R Firmiss; Natalie A Kukulka; Megan Y Devine; Belinda Li; Edward M Gong; Robert W Dettman
Journal:  Front Pediatr       Date:  2019-11-12       Impact factor: 3.418

6.  A Novel RNA-Seq-Based Model for Preoperative Prediction of Lymph Node Metastasis in Oral Squamous Cell Carcinoma.

Authors:  Bo Qiao; Min Zhao; Jing Wu; Huan Wu; Yiming Zhao; Fanhao Meng; Yu Tian; Situo Wang; Jinlong Shi; Haizhong Zhang
Journal:  Biomed Res Int       Date:  2020-08-31       Impact factor: 3.411

  6 in total

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