Expression and correlation of MALAT1 and SOX9 in non-small cell lung cancer

被引:22
作者
Chen, Wei [1 ]
Zhao, Wei [2 ]
Chen, Sheng [3 ]
Zhang, Li [4 ]
Guo, Zhongying [5 ]
Wang, Lixin [1 ]
Wang, Jipeng [1 ]
Wan, Zongren [1 ]
Hong, Yongqing [1 ]
Yu, Liang [4 ,6 ]
机构
[1] Nanjing Med Univ, Affiliated Huaian Peoples Hosp 1, Dept Resp Med, Huaian, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Affiliated Nanjing Hosp, Dept Pathol, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Huaian Peoples Hosp 1, Dept Pulm Surg, Huaian, Jiangsu, Peoples R China
[4] Nanjing Med Univ, Affiliated Huaian Peoples Hosp 1, Dept Hematol, Huaian, Jiangsu, Peoples R China
[5] Nanjing Med Univ, Affiliated Huaian Peoples Hosp 1, Dept Pathol, Huaian, Jiangsu, Peoples R China
[6] Nanjing Med Univ, Key Lab Hematol, Nanjing, Jiangsu, Peoples R China
关键词
chemo-resistance; MALAT1; NSCLC; SOX9; LONG NONCODING RNA; AUTOSOMAL SEX REVERSAL; CAMPOMELIC DYSPLASIA; COLORECTAL-CANCER; PROSTATE-CANCER; PROGRESSION; ACTIVATION; INVASION; GENE;
D O I
10.1111/crj.12906
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
IntroductionNon-small cell lung cancer (NSCLC) is the most common cause of cancer-related deaths in the world. MALAT1 and SOX9 have important roles in tumour formation and development in several types of cancers. However, little is known about the function and co-relationship of these 2 factors in NSCLC in vivo. ObjectivesTo explore the role of MALAT1 and SOX9 expression relationship, their clinical pathological characteristics and OS on NSCLC patients. MethodsPaired of primary lung cancer tissues and the matched tumour adjacent tissues were collected in 121 NSCLC patients. MALAT1 and SOX9 mRNA expression was measured by SYBR green q RT-PCR assay. SOX-9 protein expression was measured by streptavidin-peroxidase (SP) staining method. ResultsMALAT1and SOX9 expression was higher in NSCLC tissues than the adjacent tissues, and they have positive correlation. Moreover, SOX9 protein expression was higher in NSCLC tissues, especially in MALAT1 mRNA higher expressed NSCLC tissues. MALAT1 and SOX9 mRNA expression were associated with age (x(2)=11.474, P=.009), tumour size (x(2)=26.839, P=.000), TNM stage (x(2)=8.010, P=.046) and LEL. (x(2)=53.908, P=.000). NSCLC patients with higher MALAT1 and SOX9 mRNA expression had poorer OS rates. ConclusionsMALAT1 and SOX9 could be used as prognostic co-biomarker in NSCLC.
引用
收藏
页码:2284 / 2291
页数:8
相关论文
共 40 条
[1]   Expression and Therapeutic Potential of SOX9 in Chordoma [J].
Chen, Hua ;
Garbutt, Cassandra C. ;
Spentzos, Dimitrios ;
Choy, Edwin ;
Hornicek, Francis J. ;
Duan, Zhenfeng .
CLINICAL CANCER RESEARCH, 2017, 23 (17) :5176-5186
[2]   MALAT1-miR-101-SOX9 feedback loop modulates the chemo-resistance of lung cancer cell to DDP via Wnt signaling pathway [J].
Chen, Wei ;
Zhao, Wei ;
Zhang, Li ;
Wang, Lixin ;
Wang, Jipeng ;
Wan, Zongren ;
Hong, Yongqing ;
Yu, Liang .
ONCOTARGET, 2017, 8 (55) :94317-94329
[3]   MALAT1 induced migration and invasion of human breast cancer cells by competitively binding miR-1 with cdc42 [J].
Chou, Jinjiang ;
Wang, Bingyu ;
Zheng, Tianjing ;
Li, Xiaoman ;
Zheng, Lufeng ;
Hu, Jinhang ;
Zhang, Yan ;
Xing, Yingying ;
Xi, Tao .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2016, 472 (01) :262-269
[4]   Landscape of transcription in human cells [J].
Djebali, Sarah ;
Davis, Carrie A. ;
Merkel, Angelika ;
Dobin, Alex ;
Lassmann, Timo ;
Mortazavi, Ali ;
Tanzer, Andrea ;
Lagarde, Julien ;
Lin, Wei ;
Schlesinger, Felix ;
Xue, Chenghai ;
Marinov, Georgi K. ;
Khatun, Jainab ;
Williams, Brian A. ;
Zaleski, Chris ;
Rozowsky, Joel ;
Roeder, Maik ;
Kokocinski, Felix ;
Abdelhamid, Rehab F. ;
Alioto, Tyler ;
Antoshechkin, Igor ;
Baer, Michael T. ;
Bar, Nadav S. ;
Batut, Philippe ;
Bell, Kimberly ;
Bell, Ian ;
Chakrabortty, Sudipto ;
Chen, Xian ;
Chrast, Jacqueline ;
Curado, Joao ;
Derrien, Thomas ;
Drenkow, Jorg ;
Dumais, Erica ;
Dumais, Jacqueline ;
Duttagupta, Radha ;
Falconnet, Emilie ;
Fastuca, Meagan ;
Fejes-Toth, Kata ;
Ferreira, Pedro ;
Foissac, Sylvain ;
Fullwood, Melissa J. ;
Gao, Hui ;
Gonzalez, David ;
Gordon, Assaf ;
Gunawardena, Harsha ;
Howald, Cedric ;
Jha, Sonali ;
Johnson, Rory ;
Kapranov, Philipp ;
King, Brandon .
NATURE, 2012, 489 (7414) :101-108
[5]   MALAT1- a paradigm for long noncoding RNA function in cancer [J].
Gutschner, Tony ;
Haemmerle, Monika ;
Diederichs, Sven .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2013, 91 (07) :791-801
[6]   Lung cancer: current therapies and new targeted treatments [J].
Hirsch, Fred R. ;
Scagliotti, Giorgio V. ;
Mulshine, James L. ;
Kwon, Regina ;
Curran, Walter J. ;
Wu, Yi-Long ;
Paz-Ares, Luis .
LANCET, 2017, 389 (10066) :299-311
[7]   Functional and prognostic significance of long non-coding RNA MALAT1 as a metastasis driver in ER negative lymph node negative breast cancer [J].
Jadaliha, Mahdieh ;
Zong, Xinying ;
Malakar, Pushkar ;
Ray, Tania ;
Singh, Deepak K. ;
Freier, Susan M. ;
Jensen, Tor ;
Prasanth, Supriya G. ;
Karni, Rotem ;
Ray, Partha S. ;
Prasanth, Kannanganattu V. .
ONCOTARGET, 2016, 7 (26) :40418-40436
[8]   Oct4 transcriptionally regulates the expression of long non-coding RNAs NEAT1 and MALAT1 to promote lung cancer progression [J].
Jen, Jayu ;
Tang, Yen-An ;
Lu, Ying-Hung ;
Lin, Che-Chung ;
Lai, Wu-Wei ;
Wang, Yi-Ching .
MOLECULAR CANCER, 2017, 16
[9]   MALAT-1, a novel noncoding RNA, and thymosin β4 predict metastasis and survival in early-stage non-small cell lung cancer [J].
Ji, P ;
Diederichs, S ;
Wang, WB ;
Böing, S ;
Metzger, R ;
Schneider, PM ;
Tidow, N ;
Brandt, B ;
Buerger, H ;
Bulk, E ;
Thomas, M ;
Berdel, WE ;
Serve, H ;
Müller-Tidow, C .
ONCOGENE, 2003, 22 (39) :8031-8041
[10]   Chemokine (C-C Motif) Ligand 5 is Involved in Tumor-Associated Dendritic Cell-Mediated Colon Cancer Progression Through Non-Coding RNA MALAT-1 [J].
Kan, Jung-Yu ;
Wu, Deng-Chyang ;
Yu, Fang-Jung ;
Wu, Cheng-Ying ;
Ho, Ya-Wen ;
Chiu, Yen-Jung ;
Jian, Shu-Fang ;
Hung, Jen-Yu ;
Wang, Jaw-Yuan ;
Kuo, Po-Lin .
JOURNAL OF CELLULAR PHYSIOLOGY, 2015, 230 (08) :1883-1894