期刊论文详细信息
BMC Medical Genetics
Expression analysis of genes and pathways associated with liver metastases of the uveal melanoma
Jianhong Zhang3  Lei Chen2  Yong Yang1  Yuanyuan Zhang3 
[1] Department of Thoracic Surgery, Shanghai Pulmonary Hospital, Shanghai 200433, China;Department of Ophthalmology, The First Hospital of China Medical University, Shenyang 110001, China;Department of Ophthalmology, The branch of the first people’s hospital of Shanghai, Shanghai 200081, China
关键词: Pathway analysis;    GO analysis;    Gene expression;    Liver metastases;    Uveal melanoma;   
Others  :  1092294
DOI  :  10.1186/1471-2350-15-29
 received in 2012-12-29, accepted in 2014-02-12,  发布年份 2014
PDF
【 摘 要 】

Background

Uveal melanoma is an aggressive cancer which has a high percentage metastasizing to the liver, with a worse prognosis. Identification of patients at high risk of metastases may provide information for early detection of metastases and treatment.

Methods

Expression profiling of ocular tumor tissues from 46 liver metastatic uveal melanoma samples and 45 non-metastatic uveal melanoma samples were got from GEO database. Bioinformatic analyses such as the Gene Oncology and Kyoto Encyclopedia of Genes and Genomes were used to identify genes and pathways specifically associated with liver metastases of the uveal melanoma.

Results

A total of 1138 probes were differentially expressed in two group samples. All differential gene interactions in the Signal-Net were analyzed. Of them, 768 probes were up-regulated and 370 down-regulated. They mainly participated in 125 GO terms and 16 pathways. Of the genes differentially expressed between two group cancers, HTR2B, CHL1, the ZNF family, YWHAZ and FYN were the most significantly altered.

Conclusions

Bioinformatics may help excavate and analyze large amounts of data in microarrays by means of rigorous experimental planning, scientific statistical analysis and collection of complete data about liver metastases of uveal melanoma patients. In the present study, a novel differential gene expression pattern was constructed and advanced study will provide new targets for diagnosis and mechanism of uveal melanoma liver metastases.

【 授权许可】

   
2014 Zhang et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20150128182155566.pdf 2226KB PDF download
Figure 3. 129KB Image download
Figure 2. 57KB Image download
Figure 1. 555KB Image download
【 图 表 】

Figure 1.

Figure 2.

Figure 3.

【 参考文献 】
  • [1]Shields JA, Shields CL, De Potter P, Singh AD: Diagnosis and treatment of uveal melanoma. Semin Oncol 1996, 23(6):763-767.
  • [2]Sibbritt T, Patel HR, Preiss T: Mapping and significance of the mRNA methylome. Wiley Interdiscip Rev RNA 2013, 4(4):397-422.
  • [3]Trolet J, Hupe P, Huon I, Lebigot I, Decraene C, Delattre O, Sastre-Garau X, Saule S, Thiery JP, Plancher C, Asselain B, Desjardins L, Mariani P, Piperno-Neumann S, Barillot E, Couturier J: Genomic profiling and identification of high-risk uveal melanoma by array CGH analysis of primary tumors and liver metastases. Invest Ophthalmol Vis Sci 2009, 50(6):2572-2580.
  • [4]Augsburger JJ, Correa ZM, Shaikh AH: Effectiveness of treatments for metastatic uveal melanoma. Am J Ophthalmol 2009, 148(1):119-127.
  • [5]Onken MD, Worley LA, Ehlers JP, Harbour JW: Gene expression profiling in uveal melanoma reveals two molecular classes and predicts metastatic death. Cancer Res 2004, 64(20):7205-7209.
  • [6]Onken MD, Ehlers JP, Worley LA, Makita J, Yokota Y, Harbour JW: Functional gene expression analysis uncovers phenotypic switch in aggressive uveal melanomas. Cancer Res 2006, 66(9):4602-4609.
  • [7]Petrausch U, Martus P, Tonnies H, Bechrakis NE, Lenze D, Wansel S, Hummel M, Bornfeld N, Thiel E, Foerster MH, Keilholz U: Significance of gene expression analysis in uveal melanoma in comparison to standard risk factors for risk assessment of subsequent metastases. Eye (Lond) 2008, 22(8):997-1007.
  • [8]Mallikarjuna K, Pushparaj V, Biswas J, Krishnakumar S: Expression of epidermal growth factor receptor, ezrin, hepatocyte growth factor, and c-Met in uveal melanoma: an immunohistochemical study. Curr Eye Res 2007, 32(3):281-290.
  • [9]Di Cesare S, Marshall JC, Logan P, Antecka E, Faingold D, Maloney SC, Burnier MN Jr: Expression and migratory analysis of 5 human uveal melanoma cell lines for CXCL12, CXCL8, CXCL1, and HGF. J Carcinog 2007, 6:2.
  • [10]Peruzzi B, Bottaro DP: Targeting the c-met signaling pathway in cancer. Clin Cancer Res 2006, 12(12):3657-3660.
  • [11]All-Ericsson C, Girnita L, Seregard S, Bartolazzi A, Jager MJ, Larsson O: Insulin-like growth factor-1 receptor in uveal melanoma: a predictor for metastatic disease and a potential therapeutic target. Invest Ophthalmol Vis Sci 2002, 43(1):1-8.
  • [12]Mouriaux F, Kherrouche Z, Maurage CA, Demailly FX, Labalette P, Saule S: Expression of the c-kit receptor in choroidal melanomas. Melanoma Res 2003, 13(2):161-166.
  • [13]Mouriaux F, Chahud F, Maurage CA, Malecaze F, Labalette P: Implication of stem cell factor in the proliferation of choroidal melanocytes. Exp Eye Res 2001, 73(2):151-157.
  • [14]Lefevre G, Glotin AL, Calipel A, Mouriaux F, Tran T, Kherrouche Z, Maurage CA, Auclair C, Mascarelli F: Roles of stem cell factor/c-Kit and effects of Glivec/STI571 in human uveal melanoma cell tumorigenesis. J Biol Chem 2004, 279(30):31769-31779.
  • [15]Scala S, Ierano C, Ottaiano A, Franco R, La Mura A, Liguori G, Mascolo M, Staibano S, Ascierto PA, Botti G, De Rosa G, Castello G: CXC chemokine receptor 4 is expressed in uveal malignant melanoma and correlates with the epithelioid-mixed cell type. Cancer Immunol Immunother 2007, 56(10):1589-1595.
  • [16]Franco R, Botti G, Mascolo M, Loquercio G, Liguori G, Ilardi G, Losito S, La Mura A, Calemma R, Ierano C, Bryce J, D'Alterio C, Scala S: CXCR4-CXCL12 and VEGF correlate to uveal melanoma progression. Front Biosci (Elite Ed) 2010, 2:13-21.
  • [17]Gangemi R, Mirisola V, Barisione G, Fabbi M, Brizzolara A, Lanza F, Mosci C, Salvi S, Gualco M, Truini M, Angelini G, Boccardo S, Cilli M, Airoldi I, Queirolo P, Jager MJ, Daga A, Pfeffer U, Ferrini S: Mda-9/syntenin is expressed in uveal melanoma and correlates with metastatic progression. Plos One 2012, 7(1):e29989.
  • [18]Laurent C, Valet F, Planque N, Silveri L, Maacha S, Anezo O, Hupe P, Plancher C, Reyes C, Albaud B, Rapinat A, Gentien D, Couturier J, Sastre-Garau X, Desjardins L, Thiery JP, Roman-Roman S, Asselain B, Barillot E, Piperno-Neumann S, Saule S: High PTP4A3 phosphatase expression correlates with metastatic risk in uveal melanoma patients. Cancer Res 2011, 71(3):666-674.
  • [19]Jeanmougin M, de Reynies A, Marisa L, Paccard C, Nuel G, Guedj M: Should we abandon the t-test in the analysis of gene expression microarray data: a comparison of variance modeling strategies. Plos One 2010, 5(9):e12336.
  • [20]Eisen MB, Spellman PT, Brown PO, Botstein D: Cluster analysis and display of genome-wide expression patterns. Proc Natl Acad Sci U S A 1998, 95(25):14863-14868.
  • [21]Dennis G Jr, Sherman BT, Hosack DA, Yang J, Gao W, Lane HC, Lempicki RA: DAVID: database for annotation, visualization, and integrated discovery. Genome Biol 2003, 4(5):3. BioMed Central Full Text
  • [22]Khatri P, Draghici S, Ostermeier GC, Krawetz SA: Profiling gene expression using onto-express. Genomics 2002, 79(2):266-270.
  • [23]Draghici S, Khatri P, Martins RP, Ostermeier GC, Krawetz SA: Global functional profiling of gene expression. Genomics 2003, 81(2):98-104.
  • [24]Soll C, Jang JH, Riener MO, Moritz W, Wild PJ, Graf R, Clavien PA: Serotonin promotes tumor growth in human hepatocellular cancer. Hepatology 2010, 51(4):1244-1254.
  • [25]Long MJ, Wu FX, Li P, Liu M, Li X, Tang H: MicroRNA-10a targets CHL1 and promotes cell growth, migration and invasion in human cervical cancer cells. Cancer Lett 2012, 324(2):186-196.
  • [26]Yajima I, Kumasaka M, Thang ND, Yanagishita T, Ohgami N, Kallenberg D, Naito Y, Yoshikawa T, Sakashita N, Kato M: Zinc finger protein 28 as a novel melanoma-related molecule. J Dermatol Sci 2009, 55(1):68-70.
  • [27]Lovering RC, Camon EB, Blake JA, Diehl AD: Access to immunology through the gene ontology. Immunology 2008, 125(2):154-160.
  • [28]Guo CJ, Pan Q, Li DG, Sun H, Liu BW: miR-15b and miR-16 are implicated in activation of the rat hepatic stellate cell: an essential role for apoptosis. J Hepatol 2009, 50(4):766-778.
  • [29]Yu SC, Leung TW, Lee KT, Wong LK: Angioplasty and stenting of intracranial atherosclerosis with the wingspan system: 1-year clinical and radiological outcome in a single Asian center. J Neurointerv Surg 2014, 6:96-102.
  • [30]Armstrong SR, Campbell CB, Richardson CL, Vickery RG, Tsuruda PR, Long DD, Hegde SS, Beattie DT: The in vivo pharmacodynamics of the novel opioid receptor antagonist, TD-1211, in models of opioid-induced gastrointestinal and CNS activity. Naunyn Schmiedebergs Arch Pharmacol 2013, 386(6):471-478.
  • [31]Festa F, Steel J, Bian X, Labaer J: High-throughput cloning and expression library creation for functional proteomics. Proteomics 2013, 13(9):1381-1399.
  • [32]Lublin FD: MS as a gateway disease. J Neurol Sci 2013, 333(1-2):73-75.
  • [33]Grana RA: Electronic cigarettes: a new nicotine gateway? J Adolesc Health 2013, 52(2):135-136.
  • [34]Shukla S, Chandran S, Gadagkar R: Ovarian developmental variation in the primitively eusocial wasp ropalidia marginata suggests a gateway to worker ontogeny and the evolution of sociality. J Exp Biol 2013, 216(Pt 2):181-187.
  • [35]Mueller MB, Blunk T, Appel B, Maschke A, Goepferich A, Zellner J, Englert C, Prantl L, Kujat R, Nerlich M, Angele P: Insulin is essential for in vitro chondrogenesis of mesenchymal progenitor cells and influences chondrogenesis in a dose-dependent manner. Int Orthop 2013, 37(1):153-158.
  • [36]Chen CH, Chuang SM, Yang MF, Liao JW, Yu SL, Chen JJ: A novel function of YWHAZ/beta-catenin axis in promoting epithelial-mesenchymal transition and lung cancer metastasis. Mol Cancer Res 2012, 10(10):1319-1331.
  • [37]Chua SL, See Too WC, Khoo BY, Few LL: UBC and YWHAZ as suitable reference genes for accurate normalisation of gene expression using MCF7, HCT116 and HepG2 cell lines. Cytotechnology 2011, 63(6):645-654.
  • [38]Wang Q, Qian J, Wang F, Ma Z: Cellular prion protein accelerates colorectal cancer metastasis via the Fyn-SP1-SATB1 axis. Oncol Rep 2012, 28(6):2029-2034.
  • [39]Yadav V, Denning MF: Fyn is induced by Ras/PI3K/Akt signaling and is required for enhanced invasion/migration. Mol Carcinog 2011, 50(5):346-352.
  • [40]Kim AN, Jeon WK, Lim KH, Lee HY, Kim WJ, Kim BC: Fyn mediates transforming growth factor-beta1-induced down-regulation of E-cadherin in human A549 lung cancer cells. Biochem Biophys Res Commun 2011, 407(1):181-184.
  文献评价指标  
  下载次数:51次 浏览次数:18次