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FGF4在肺癌细胞体内和体外中表达差异的研究 被引量:6

Differential Expression of FGF4 between in vivo and in vitro Lung Cancer Cells
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摘要 FGF4已经被证明是癌基因,它涉及肿瘤的生长和转移,为了解FGF4的表达与肿瘤微环境的关系。我们利用FGF4抗体通过免疫组化对一名肺癌患者癌旁,癌组织,癌组织小鼠移植瘤,二次移植瘤以及原代培养的细胞爬片进行FGF4检测,探究其表达差异。通过对比癌组织与对照组(癌旁组织),FGF4在癌巢中高表达;同样,移植瘤与二次移植瘤的癌巢中与癌旁组织比较,FGF4表达相对较高;但是将癌组织进行原代培养后,免疫组化检测细胞爬片FGF4,发现仅有5%±0.21%的肿瘤细胞表达FGF4,对照蛋白Cytokine作为肿瘤标记物,则在100%的肿瘤细胞中表达。研究提示免疫组化检测到FGF4在体内和体外表达不同,提示肿瘤细胞FGF4的表达与肿瘤微环境调控密切相关,肿瘤微环境对肿瘤细胞的FGF4的调控有着重要作用。 FGF4 is regarded as an oncogene involved in tumor growth, metastasis. To assess its role in the interaction between tumor and the microenvironment, immunohistochemistry analysis was performed on normal tissue,tumor tissue, tumor Xenografts in mice with FGF4 antibody to examine FGF4 expression in vivo. Results show that FGF4 is up-regulation in carcinoma nest compared with adjacent tissues; Similarly, Two kinds of xenografts displayed also high FGF4 expression whereas lower level was detected in paracancer tissues. Interestingly, in vitro, only5%±0.21% of cultured cancer cell deriving from the same patient expressed high level of FGF4. As contrast, Cytokine was expressed in 100% tumor cells. Taken together, these results suggest that FGF4 in tumor cell might play a role in the interaction with tumor microenvironment.
出处 《基因组学与应用生物学》 CAS CSCD 北大核心 2014年第3期501-504,共4页 Genomics and Applied Biology
基金 广东省高等学校学科与专业建设专项资金(2013KJCX0108) 国家自然基金(31271455)共同资助
关键词 FGF4 小鼠移植瘤 肺癌 肿瘤微环境 FGF4 Xenografted tumor None small cell lung cancer Tumor microenvironment
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  • 1Al-Salahi O.S., Ji D., Majid A.M., Kit-Lam C., Abdullah W.Z., Zaki A., Jamal Din S.K., Yusoff N.M., and Majid A.S., 2014, Anti-tumor activity of Eurycoma longifolia root ex- tracts against I(-562 cell line: In vitro and in vivo study, PLoS One, 9:e83818.
  • 2Allen B.L., Filla M.S., and Rapraeger A.C., 2001, Role of hep- aran sulfate as a tissue-specific regulator of FGF-4 and FGF receptor recognition, J. Cell Biol., 155(5): 845-858.
  • 3Benveniste P., Serra P., Dervovic D., Herer E., Knowles G., Mo- htashami M., and Zfifiiga-Pflticker J.C., 2014, Notch signals are required for in vitro but not in vivo maintenance of hu-man hematopoietic stem cells and delay the appearance of multipotent progenitors, Blood, 123(8): 1167-1177.
  • 4Farre J., Roura S., Prat-Vidal C., Soler-Botija C., Llach A., Moli- na C.E., Hove-Madsen L., Cair6 J.J., Gbdia F., Brag6s R., Cinca J., and Bayes-Genis A., 2007, FGF-4 increases in vitro expansion rate of human adult bone marrow-derived mes- enchymal stem cells, Growth Factors, 25(2): 71-76.
  • 5Feldman B., Poueymirou W., Papaioannou V.E., DeChiara T.M., and Goldfarb M., 1995, Requirement of FGF-4 for postim- plantation mouse development, Science, 267(5195): 246-249.
  • 6Galland F., Stefanova M., Lafage M., and Bimbaum D., 1992, Localization of the 5' end of the MCF2 oncogene to human chromosome 15q15-q23, Cytogenetics and Cell Genetics, 60(2): 114-116.
  • 7Hirai K., Sasaki H., Yamamoto H., Sakarnoto H., Kubota Y., Kakizoe T., Terada M., and Ochiya T., 2004, HST-1/FGF-4 protects male germ cells from apoptosis under heat-stress condition, Exp. Cell Res., 294(1): 77-85.
  • 8Li F., Dong L., Xing R., Wang L., Luan F., Yao C., Ji X., and Bai L., 2014, Homeobox B9 is overexpressed in hepatocellular carcinomas and promotes tumor cell proliferation both in vitro and in vivo, Biochem. Biophys. Res. Commun., 444(2): 241-247.
  • 9Lu T., Yang C., Sun H., Lv J., Zhang F., and Dong X.J., 2014, FGF4 and HGF promote differentiation of mouse bone mar- row mesenchymal stem cells into hepatocytes via the MAPK pathway, Genetics and Molecular Research, 13(1): 415-424.
  • 10Mayshar Y., Rom E., Chumakov I., Kronman A., Yayon A., and Benvenisty N., 2008, Fibroblast growth factor 4 and its novel splice isoform have opposing effects on the maintenance of human embryonic stem cell self-renewal, Stem Cells, 26(3): 767-774.

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