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胃腺癌中ROS1基因重排及其临床意义 被引量:1

Clinical Significance of ROS1 Rearrangements in Human Gastric Adenocarcinomas Cancer
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摘要 目的分析ROS1基因重排与胃腺癌临床病理学指标的关系。方法应用荧光原位杂交技术(FISH),检测60例胃腺癌肿瘤组织中ROS1基因的重排;采用siRNA和Real-time PCR检测ROS1重排与胃癌细胞免疫反应的关键分子的关系。结果胃腺癌组织中ROS1基因重排发生率为1.7%(1/60)。ROS1基因高表达与胃肿瘤淋巴结转移呈正相关(P<0.05),但与患者性别、年龄、发生部位、肿瘤直径、Laurén分类、病理分级、HP感染、浸润深度和TNM分期等无关。ROS1阳性表达肿瘤组织中IL-6、TNF-α阳性表达率明显高于ROS1阴性组织。结论 ROS1基因重排可能与炎症因子基因协同发挥促癌作用。 Objective To investigate the relationship between ROS 1 rearrangements and clinicopathological indicators in gastric adenocarcinomas. Methods ROS1 rearrangements in 60 cases of gastric adenocarcinoma tissues were detected by fluores-cence in situ hybridization ( FISH), and the relationship between ROS 1 rearrangements and key moleculars of immune response in gastric cancer were detected by siRNA and RT-PCR.Results The incidence rate of ROS1 gene rearrangement in gastric cancer was 1.7%(1/60).And the high expression of ROS1 was positively related with lymph node metastasis in gastric tumors, but had no correlation with gender, age,location,diameter,Laur én classification,pathological grade,HP infection,depth of invasion and TNM stageing(P>0.05).But which were correlated with lymph node metastasis (P<0.05).The positive expression of IL-6 and TNF-αin the ROS1 positive group was significantly higher than that of ROS 1 negative group. Conclusion ROS1 gene rearrange-ment may collaborate with inflammatory cytokines gene on tumor promotion.
出处 《实用癌症杂志》 2014年第11期1386-1389,共4页 The Practical Journal of Cancer
关键词 ROS1 基因重排 胃腺癌 肿瘤坏死因子Α 白细胞介素6 ROS1 Gene rearrangement Gastric adencarcinomas TNF-α IL-6
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  • 1Gu Ting-Lei,Deng Xiaxing,Huang Feizhou,Tucker Meghan,Crosby Katherine,Rimkunas Victoria,Wang Yi,Deng Gang,Zhu Lei,Tan Zhiping,Hu Yerong,Wu Chunlin,Nardone Julie,MacNeill Joan,Ren Jianmin,Reeves Cynthia,Innocenti Gregory,Norris Brett,Yuan.Survey of tyrosine kinase signaling reveals ROS kinase fusions in human cholangiocarcinoma. PloS one . 2011
  • 2McDermott Ultan,Iafrate A John,Gray Nathanael S,Shioda Toshi,Classon Marie,Maheswaran Shyamala,Zhou Wenjun,Choi Hwan Geun,Smith Shannon L,Dowell Lori,Ulkus Lindsey E,Kuhlmann Georgiana,Greninger Patricia,Christensen James G,Haber Daniel A,S.Genomic alterations of anaplastic lymphoma kinase may sensitize tumors to anaplastic lymphoma kinase inhibitors. Cancer Research . 2008
  • 3Megan L. Peach,Nelly Tan,Sarah J. Choyke,Alessio Giubellino,Gagani Athauda,Terrence R. Burke,Jr.,Marc C. Nicklaus,Donald P. Bottaro.Directed Discovery of Agents Targeting the Met Tyrosine Kinase Domain by Virtual Screening. Journal of Medicinal Chemistry . 2009
  • 4Kim HR,Lim SM,Kim HJ,et al.The frequency and impact of ROS1 rearrangement on clinical outcomes in never smokers with lung adenocarcinoma. Annals of Oncology . 2013
  • 5Kristin Bergethon,Alice T. Shaw,Sai-Hong Ignatius Ou.ROS1 Rearrangements Define a Unique Molecular Class of Lung Cancers. Journal of Clinical Oncology . 2012
  • 6Fan H,Hall P,Santos L L, et al.Macrophage migration inhibitory factor and CD74regulatemacrophage chemotactic responses via MAPK and Rho GTPase. J Immunol . 2011
  • 7Birchmeier C,Sharma S,Wigler M.Expression and rearrangement of the ROS1 gene in human glioblastoma cells. Proceedings of the National Academy of Sciences of the United States of America . 1987
  • 8Cai W,Li X,Su C,et al.ROS1 fusions in Chinese patients with non-smallcell lung cancer. Annals of Oncology . 2013
  • 9AlainCharest,KearaLane,KevinMcMahon,JuliePark,ElizabethPreisinger,HelenConroy,DavidHousman.Fusion of FIG to the receptor tyrosine kinase ROS in a glioblastoma with an interstitial del(6)(q21q21)[J]. Genes Chromosom. Cancer . 2003 (1)
  • 10El-Deeb IM,Yoo KH,Lee SH.ROS receptor tyrosine kinase:a new potential target for anticancer drugs. Medicinal Research Reviews . 2011

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  • 1Siegel RL( Miller KD, Jemal A. Cancer statistics, 2015[J]. CA Cancer JClin, 2015, 65(1):5-29.
  • 2DeSantis CE, Lin CC, Mariotto AB, et al. Cancer treatment andsurvivorship statistics, 2014[J]. CA Cancer J Clin, 2014, 64(4):252-271.
  • 3Davidson MR, Gazdar AF, Clarke BE. The pivotal role of pathologyin the management of lung cancer[J]. J Thorac Dis, 2013, 5 Suppl 5:S463-S478.
  • 4Sher T, Dy GK, Adjei AA. Small cell lung cancer[J]. Mayo Clin Proc,2008, 83(3):355-367.
  • 5Mok TS, Wu YL, Thongprasert S, et al. Gefitinib or carboplatin-paclitaxel in pulmonary adenocarcinoma [J]. N Engl J Med, 2009,361(10):947-957.
  • 6Maemondo M, Inoue A, Kobayashi K, et al. Gefitinib or chemotherapyfor non-small-cell lung cancer with mutated EGFR[J]. N Engl J Med,2010, 362(25):2380-2388.
  • 7Mitsudomi T, Morita S, Yatabe Y, et al. Gefitinib versus cisplatin plusdocetaxel in patients with non-small-cell lung cancer harbouringmutations of the epidermal growth factor receptor (WJTOG3405): anopen label, randomised phase 3 trial[J]. Lancet Oncol, 2010, 11(2):121-128.
  • 8Zhou C, Wu YL, Chen G, et al. Erlotinib versus chemotherapy as first-line treatment for patients with advanced EGFR mutation-positive non-small-cell lung cancer (OPTIMAL, CTONG-0802): a multicentre,open-label, randomised, phase 3 study[J]. Lancet Oncol, 2011,12(8):735-742.
  • 9Rosell R, Carcereny E, Gervais R, et al. Erlotinib versus standard chemotherapy as first-line treatment for European patients with advanced EGFR mutation-positive non-small-cell lung cancer (EURTAC): a multicentre, open-label, randomised phase 3 trial[J]. Lancet Oncol, 2012, 13(3): 239-246.
  • 10Wu YL, Zhou C, Liam CK, et al. First-line erlotinib versus gemcitabine/cisplatin in patients with advanced EGFR mutation-positive non-small-cell lung cancer: analyses from the phase III, randomized, open-label,ENSURE study [J]. Ann Oncol, 2015, 26(9): 18834889.

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