Literature DB >> 25567207

Increased expression of SOX4 is a biomarker for malignant status and poor prognosis in patients with non-small cell lung cancer.

Dingmiao Wang1, Ting Hao, Yang Pan, Xiaowei Qian, Daixing Zhou.   

Abstract

The aim of the present study was to analyze the expression of sex-determining region Y-related high mobility group box 4 (SOX4) in non-small cell lung cancer (NSCLC) and its correlation with clinicopathologic characteristics, including the survival of NSCLC patients. To observe initially the expression status of SOX4 in lung squamous cell carcinoma and adenocarcinoma at gene expression omnibus. The expression of SOX4 mRNA and protein was examined in NSCLC tissues and normal lung tissues through real-time PCR and immunohistochemistry. Meanwhile, the relationship of SOX4 expression levels with clinical characteristics of 168 NSCLC patients was analyzed by immunohistochemistry. Univariate and multivariate analyses were performed to determine the association between SOX4 expression and prognosis of NSCLC patients. In our results, SOX4 expression was increased in NSCLC tissues compared with paired normal lung tissues in microarray data (GSE3268). SOX4 mRNA and protein expression were markedly higher in NSCLC tissues than in normal lung tissues (P = 0.001 and P = 0.001, respectively). Using immunohistochemistry, high levels of SOX4 protein were positively correlated with status of differentiated degree (high vs. middle, P = 0.004; high vs. low, P < 0.001), clinical stage (I-II vs. III-IV, P < 0.001), T classification (T1-T2 vs. T3-T4, P = 0.004), N classification (N0-N1 vs. N2-N3, P = 0.002), and M classification (M0 vs. M1, P = 0.011) in NSCLC. Moreover, the higher level of SOX4 expression was markedly correlated with poor overall survival in NSCLC patients (P < 0.001). Multivariate analysis suggested that increased SOX4 expression was a poor independent prognostic predictor for NSCLC patients (P = 0.002). In conclusion, SOX4 plays an important role on NSCLC progression and prognosis and may serve as a convictive prognostic biomarker for NSCLC patients.

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Year:  2015        PMID: 25567207     DOI: 10.1007/s11010-014-2315-9

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  37 in total

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2.  SOX4 overexpression regulates the p53-mediated apoptosis in hepatocellular carcinoma: clinical implication and functional analysis in vitro.

Authors:  Wonhee Hur; Hyangshuk Rhim; Chan Kwon Jung; Jin Dong Kim; Si Hyun Bae; Jeong Won Jang; Jin Mo Yang; Seong-Taek Oh; Dong Goo Kim; Hee Jung Wang; Sean Bong Lee; Seung Kew Yoon
Journal:  Carcinogenesis       Date:  2010-04-16       Impact factor: 4.944

3.  Prognostic significance of Sox4 expression in human cutaneous melanoma and its role in cell migration and invasion.

Authors:  Seyed Mehdi Jafarnejad; Aijaz Ahmad Wani; Magdalena Martinka; Gang Li
Journal:  Am J Pathol       Date:  2010-10-15       Impact factor: 4.307

4.  The Sex-determining region Y-box 4 and homeobox C6 transcriptional networks in prostate cancer progression: crosstalk with the Wnt, Notch, and PI3K pathways.

Authors:  Carlos S Moreno
Journal:  Am J Pathol       Date:  2009-12-17       Impact factor: 4.307

5.  Massively parallel signature sequencing and bioinformatics analysis identifies up-regulation of TGFBI and SOX4 in human glioblastoma.

Authors:  Biaoyang Lin; Anup Madan; Jae-Geun Yoon; Xuefeng Fang; Xiaowei Yan; Taek-Kyun Kim; Daehee Hwang; Leroy Hood; Gregory Foltz
Journal:  PLoS One       Date:  2010-04-19       Impact factor: 3.240

6.  Epigenetic repression of microRNA-129-2 leads to overexpression of SOX4 oncogene in endometrial cancer.

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Journal:  Cancer Res       Date:  2009-11-03       Impact factor: 12.701

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Journal:  Blood       Date:  2012-11-14       Impact factor: 22.113

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Journal:  Am J Pathol       Date:  2002-10       Impact factor: 4.307

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Journal:  Nature       Date:  1996-04-25       Impact factor: 49.962

10.  Dysregulation of the transcription factors SOX4, CBFB and SMARCC1 correlates with outcome of colorectal cancer.

Authors:  C L Andersen; L L Christensen; K Thorsen; T Schepeler; F B Sørensen; H W Verspaget; R Simon; M Kruhøffer; L A Aaltonen; S Laurberg; T F Ørntoft
Journal:  Br J Cancer       Date:  2009-01-20       Impact factor: 7.640

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  20 in total

1.  Molecular cloning and mRNA expression pattern of Sox4 in Misgurnus anguillicaudatus.

Authors:  Xiaohua Xia; Ruyan Wan; Weiran Huo; Linxia Zhang; Xiaopei Xia; Zhongjie Chang
Journal:  J Genet       Date:  2018-09       Impact factor: 1.166

2.  Over-expression of Sox4 and β-catenin is associated with a less favorable prognosis of osteosarcoma.

Authors:  Zheng-Qi Bao; Chang-Chun Zhang; Yu-Zhou Xiao; Jian-Sheng Zhou; Yi-Sheng Tao; Da-Min Chai
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2016-04-13

3.  MicroRNA-338-3p targets SOX4 and inhibits cell proliferation and invasion of renal cell carcinoma.

Authors:  Zhigang Tong; Xianfeng Meng; Jinsong Wang; Lixin Wang
Journal:  Exp Ther Med       Date:  2017-09-21       Impact factor: 2.447

4.  MicroRNA-539 inhibits colorectal cancer progression by directly targeting SOX4.

Authors:  Jian Zhao; Jian Xu; Rui Zhang
Journal:  Oncol Lett       Date:  2018-06-04       Impact factor: 2.967

5.  miR-132 inhibits lung cancer cell migration and invasion by targeting SOX4.

Authors:  Yang Li; Lingling Zu; Yuli Wang; Min Wang; Peirui Chen; Qinghua Zhou
Journal:  J Thorac Dis       Date:  2015-09       Impact factor: 2.895

6.  MiR-211 inhibits cell proliferation and invasion of gastric cancer by down-regulating SOX4.

Authors:  Chen-Yu Wang; Long Hua; Juan Sun; Kun-Hou Yao; Jiang-Tao Chen; Jun-Jie Zhang; Jun-Hong Hu
Journal:  Int J Clin Exp Pathol       Date:  2015-11-01

7.  MicroRNA-30a functions as tumor suppressor and inhibits the proliferation and invasion of prostate cancer cells by down-regulation of SIX1.

Authors:  Qinghuan Zhu; Hongzhi Li; Yingjie Li; Lining Jiang
Journal:  Hum Cell       Date:  2017-06-01       Impact factor: 4.174

8.  SOX4 arrests lung development in rats with hyperoxia‑induced bronchopulmonary dysplasia by controlling EZH2 expression.

Authors:  Bingting Pan; Xindong Xue; Dan Zhang; Mengyun Li; Jianhua Fu
Journal:  Int J Mol Med       Date:  2017-10-03       Impact factor: 4.101

9.  GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer.

Authors:  Maxine M Chen; Tracy A O'Mara; Deborah J Thompson; Jodie N Painter; John Attia; Amanda Black; Louise Brinton; Stephen Chanock; Chu Chen; Timothy Ht Cheng; Linda S Cook; Marta Crous-Bou; Jennifer Doherty; Christine M Friedenreich; Montserrat Garcia-Closas; Mia M Gaudet; Maggie Gorman; Christopher Haiman; Susan E Hankinson; Patricia Hartge; Brian E Henderson; Shirley Hodgson; Elizabeth G Holliday; Pamela L Horn-Ross; David J Hunter; Loic Le Marchand; Xiaolin Liang; Jolanta Lissowska; Jirong Long; Lingeng Lu; Anthony M Magliocco; Lynn Martin; Mark McEvoy; Sara H Olson; Irene Orlow; Loreall Pooler; Jennifer Prescott; Radhai Rastogi; Timothy R Rebbeck; Harvey Risch; Carlotta Sacerdote; Frederick Schumacher; Veronica Wendy Setiawan; Rodney J Scott; Xin Sheng; Xiao-Ou Shu; Constance Turman; David Van Den Berg; Zhaoming Wang; Noel S Weiss; Nicholas Wentzensen; Lucy Xia; Yong-Bing Xiang; Hannah P Yang; Herbert Yu; Wei Zheng; Paul D P Pharoah; Alison M Dunning; Ian Tomlinson; Douglas F Easton; Peter Kraft; Amanda B Spurdle; Immaculata De Vivo
Journal:  Hum Mol Genet       Date:  2016-03-23       Impact factor: 6.150

10.  SOX4 contributes to the progression of cervical cancer and the resistance to the chemotherapeutic drug through ABCG2.

Authors:  R Sun; B Jiang; H Qi; X Zhang; J Yang; J Duan; Y Li; G Li
Journal:  Cell Death Dis       Date:  2015-11-19       Impact factor: 8.469

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