Literature DB >> 21264844

Independent and tissue-specific prognostic impact of miR-126 in nonsmall cell lung cancer: coexpression with vascular endothelial growth factor-A predicts poor survival.

Tom Donnem1, Kenneth Lonvik, Katrine Eklo, Thomas Berg, Sveinung W Sorbye, Khalid Al-Shibli, Samer Al-Saad, Sigve Andersen, Helge Stenvold, Roy M Bremnes, Lill-Tove Busund.   

Abstract

BACKGROUND: Angiogenesis is pivotal in tumor development. Vascular endothelial growth factor-A (VEGF-A) is considered one of the most important angiogenic factors, but lately several microRNAs (miRs) have been associated with vascular development. miR-126 has been related to tumor angiogenesis and in the regulation of VEGF-A. The authors aimed to investigate the prognostic impact of miR-126 and its co-expression with VEGF-A in nonsmall cell lung cancer (NSCLC) patients.
METHODS: Tumor tissue samples from 335 resected stage I to IIIA NSCLC patients were obtained and tissue microarrays (TMAs) were constructed with 4 cores from each tumor specimen. VEGF-A expression was evaluated by immunohistochemistry, and in situ hybridization was used to evaluate the expression of miR-126.
RESULTS: In the total material, miR-126 was a significant negative prognostic factor in both univariate (P = .005) and multivariate analyses (hazard ratio [HR] 1.8, 95% confidence interval [CI] 1.2-2.8, P = .01). Stratified by histology, miR-126 was only significant in squamous cell carcinomas (univariate: P < .001; multivariate: HR 3.1, CI 95% 1.7-5.6, P<.001). Stratified by lymph node status, miR-126 was significant only in the lymph node-positive subgroup (univariate: P<.001; multivariate: HR 4.1, CI 95% 2.0-8.4, P < .001). High miR-126 expression correlated significantly with high VEGF-A expression (P = .037). The co-expression of miR-126 and VEGF-A had a significant prognostic impact (P = .002), with 5-year survival rates of 68%, 51%, and 42% for low/low (n = 150), mixed combinations (n = 129), and high/high (n = 35) expression, respectively.
CONCLUSIONS: miR-126 is a strong and independent negative prognostic factor in NSCLC, and its prognostic impact appears related primarily to histology and nodal status.
Copyright © 2011 American Cancer Society.

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Year:  2011        PMID: 21264844     DOI: 10.1002/cncr.25907

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  41 in total

1.  Tumor microRNA-126 controls cell viability and associates with poor survival in patients with esophageal adenocarcinoma.

Authors:  Ela Toxopeus; N Lynam-Lennon; K Biermann; G Dickens; P E de Ruiter; Jjb van Lanschot; J V Reynolds; Bpl Wijnhoven; J O'Sullivan; Ljw van der Laan
Journal:  Exp Biol Med (Maywood)       Date:  2019-08-07

2.  Down-regulation of tissue microRNA-126 was associated with poor prognosis in patients with cutaneous melanoma.

Authors:  Nengxing Lin; Yu Zhou; Xin Lian; Yating Tu
Journal:  Int J Clin Exp Med       Date:  2015-03-15

3.  MicroRNA down-regulated in human cholangiocarcinoma control cell cycle through multiple targets involved in the G1/S checkpoint.

Authors:  Alexandru V Olaru; Gabriel Ghiaur; Sumitaka Yamanaka; Delgermaa Luvsanjav; Fangmei An; Irinel Popescu; Sorin Alexandrescu; Sarah Allen; Timothy M Pawlik; Michael Torbenson; Christos Georgiades; Lewis R Roberts; Gregory J Gores; Anne Ferguson-Smith; Maria I Almeida; George A Calin; Esteban Mezey; Florin M Selaru
Journal:  Hepatology       Date:  2011-12       Impact factor: 17.425

4.  Expression of microRNA miR-126 and miR-200c is associated with prognosis in patients with non-small cell lung cancer.

Authors:  Mi Kyeong Kim; Sang Bong Jung; Jong-Sik Kim; Mee Sook Roh; Ji Hyun Lee; Eun Hee Lee; Hyoun Wook Lee
Journal:  Virchows Arch       Date:  2014-08-16       Impact factor: 4.064

Review 5.  A potential role for estrogen in cigarette smoke-induced microRNA alterations and lung cancer.

Authors:  Amit Cohen; Mario Alberto Burgos-Aceves; Yoav Smith
Journal:  Transl Lung Cancer Res       Date:  2016-06

6.  Relationship of immunohistochemical biomarker expression and lymph node involvement in patients undergoing surgical treatment of NSCLC with long-term follow-up.

Authors:  Ana María Gómez; Jose Ramón Jarabo Sarceda; Jose Antonio L García-Asenjo; Cristina Fernandez; Susana Hernandez; Julian Sanz; Elena Fernandez; Joaquin Calatayud; Antonio Torres; Florentino Hernando
Journal:  Tumour Biol       Date:  2014-01-19

7.  Transfection of adenovirus-mediated mircoRNA-126 gene into infant hemangioma endothelial cells in vitro.

Authors:  Zhe Cao; Yong-Qiang Guo; Sheng-Jian Tang; Shen-Xing Tan; Chang-Ying Niu; Chun-Lei Miao; Wei Zhang; Yu-Li Li; Long Zhang; Jing-Han Wang; Xiao-Qin Liang
Journal:  Int J Clin Exp Pathol       Date:  2018-03-01

8.  Applications of MicroRNAs in the Diagnosis and Prognosis of Lung Cancer.

Authors:  Jun Shen; Feng Jiang
Journal:  Expert Opin Med Diagn       Date:  2012-05

Review 9.  Non-coding RNAs deregulation in oral squamous cell carcinoma: advances and challenges.

Authors:  T Yu; C Li; Z Wang; K Liu; C Xu; Q Yang; Y Tang; Y Wu
Journal:  Clin Transl Oncol       Date:  2015-09-14       Impact factor: 3.405

10.  Increased expression of miRNA-182 in colorectal carcinoma: an independent and tissue-specific prognostic factor.

Authors:  Shuang Wang; Min-Hui Yang; Xiao-Yan Wang; Jie Lin; Yan-Qing Ding
Journal:  Int J Clin Exp Pathol       Date:  2014-05-15
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