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趋化因子受体CXCR4在胃肠道肿瘤组织及细胞系中的异常表达 被引量:3

Aberrant expression of chemokine receptor CXCR4 in gastrointestinal cancer tissues and cancer cell lines
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摘要 目的:检测CXCR4在胃肠道肿瘤中的表达状态,探讨CXCR4在胃肠道肿瘤发病中的作用.方法:采用即时定量PCR(Real-time PCR)检测胃肠道肿瘤标本中CXCR4的表达.采用逆转录PCR(RT-PCR)和Western blot检测CXCR4在胃肠道肿瘤细胞系中的表达.结果:CXCR4mRNA在24例结直肠癌组织标本的表达水平显著高于其配对的癌旁正常组织(P<0.001).CXCR4mRNA在30例胃癌组织标本中的表达水平亦显著高于其配对的癌旁正常组织(P<0.001).CXCR4mRNA和蛋白质在结肠癌细胞系HT-29和SW-480及胃癌细胞系SGC-7901和AGS中均存在明显表达CXCR4表达与胃癌患者分期及淋巴结转移状态具有相关性(P=0.01,0.02).结论:CXCR4在胃肠道肿瘤中存在过度表达,其参与了胃肠道肿瘤的发病过程. AIM: To determine the expression status of chemokine receptor CXCR4 in gastrointestinal cancer and to explore its role in gastrointestinal carcinogenesis. METHODS: Real-time PCR was used to detect mRNA expression of CXCR4 in gastrointestinal cancer samples. Reverse-transcription PCR (RT- PCR) and Western blot were used to determine the expression of CXCR4 in gastrointestinal cancer cell lines. RESULTS: Level of CXCR4 mRNA was sig- nificantly higher in 24 colorectal cancer samples than in matched normal tissues (P 〈 0.001). Level of CXCR4 mRNA was also significantly higher in 30 gastric cancer samples than in matched normal tissues (P 〈 0.001). Both CXCR4 mRNA and CXCR4 protein were expressed strongly in colon cell lines HT-29 and SW-480, and gastric cell lines SGC-7901 and AGS. CXCR4 expression was correlated significantly with staging and lymph node metastasis in gastric cancers (P = 0.01 and P -- 0.02, respectively). CONCLUSION: CXCR4 is over-expressed in gastrointestinal cancers, and plays a role in gastrointestinal carcinogenesis.
出处 《世界华人消化杂志》 CAS 北大核心 2009年第4期421-424,共4页 World Chinese Journal of Digestology
关键词 胃肠道肿瘤 趋化因子受体 CXCR4 Gastrointestinal cancer Chemokine receptor CXCR4
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参考文献17

  • 1Kodama J, Hasengaowa, Seki N, Kusumoto T, Hiramatsu Y. Expression of the CXCR4 and CCR7 chemokine receptors in human endometrial cancer. Eur J Gynaecol Onco12007; 28:370-375
  • 2Pan J, Mestas J, Burdick MD, Phillips RJ, Thomas GV, Reckamp K, Belperio JA, Strieter RM. Stromal derived factor-1 (SDF-1/CXCL12) and CXCR4 in renal cell carcinoma metastasis. Mol Cancer 2006; 5: 56
  • 3Engl T, Relja B, Marian D, Blumenberg C, Mtiller I, Beecken WD, Jones J, Ringel EM, Bereiter-Hahn J, Jonas D, Blaheta RA. CXCR4 chemokine receptor mediates prostate tumor cell adhesion through alpha5 and beta3 integrins. Neoplasia 2006; 8: 290-301
  • 4Salvucci O, Bouchard A, Baccarelli A, Deschenes J, Sauter G, Simon R, Bianchi R, Basik M. The role of CXCR4 receptor expression in breast cancer: a large tissue microarray study. Breast Cancer Res Treat 2006; 97:275-283
  • 5Scala S, Ottaiano A, Ascierto PA, Cavalli M, Simeone E, Giuliano P, Napolitano M, Franco R, Botti G, Castello G. Expression of CXCR4 predicts poor prognosis in patients with malignant melanoma. Clin Cancer Res 2005; 11:1835-1841
  • 6Ishigami S, Natsugoe S, Nakajo A, Tokuda K, Uenosono Y, Arigami T, Matsumoto M, Okumura H, Hokita S, Aikou T. Prognostic value of CCR7 expression in gastric cancer. Hepatogastroenterology 2007; 54:1025-1028
  • 7Mashino K, Sadanaga N, Yamaguchi H, Tanaka F, Ohta M, Shibuta K, Inoue H, Mori M. Expression of chemokine receptor CCR7 is associated with lymph node metastasis of gastric carcinoma. Cancer Res 2002; 62:2937-2941
  • 8Wilson JL, Burchell J, Grimshaw MJ. Endothelins induce CCR7 expression by breast tumor cells via endothelin receptor A and hypoxia-inducible factor-1. Cancer Res 2006; 66:11802-11807
  • 9Heresi GA, Wang J, Taichman R, Chirinos JA, Regalado JJ, Lichtstein DM, Rosenblatt JD. Expression of the chemokine receptor CCR7 in prostate cancer presenting with generalized lymphadenopathy: report of a case, review of the literature, and analysis of chemokine receptor expression. Urol Onco12005; 23:261-267
  • 10Mori T, Kim J, Yamano T, Takeuchi H, Huang S, Umetani N, Koyanagi K, Hoon DS. Epigenetic upregulation of C-C chemokine receptor 7 and C-X-C chemokine receptor 4 expression in melanoma cells. Cancer Res 2005; 65:1800-1807

同被引文献48

  • 1苏丽萍,张进平,郑秀娟,储以薇,熊思东.CXCR4表达水平对肺癌细胞转移潜能的影响[J].中国肿瘤生物治疗杂志,2005,12(1):46-51. 被引量:7
  • 2Muller A, Homey B, Soto H, et al. Involvement of chemokine receptors in breast cancer metastasis. Nature, 2001, 410(6824): 50-56.
  • 3Smith JR, Falkenhagen KM, Coupland SE, et al. Malignant B cells from patients with primary central nervous system lymphoma express stroreal cell-derived factor-1. Am J Clin Pathol, 2007, 127(4): 633-641.
  • 4Alsayed Y, Ngo H, Runnels J, et al. Mechanisms of regulation of CX-CR4/SDF-1 (CXCL12) dependent migration and homing in multiple myeloma. Blood, 2007, 109(7): 2708-2717.
  • 5Kucia M, Reca R, Miekus K, et al. Trafficking of normal stem cells and metastasis of cancer stem cells involve similar mechanisms:Pivotal role of the SDF-1/CXCR4 axis. Stem cells, 2005, 23(7): 879- 894.
  • 6Corcoran KE, Trzaska KA, Fernandes H, et al. Mesenchymal stem cells in early entry of breast cancer into bone marrow. PLoS One, 2008, 3(6): e2563.
  • 7Muehlberg FL, Song YH, Krohn A, et al. Tissue-resident stem cells promote breast cancer growth and metastasis. Carcinogenesis, 2009, 30(4): 589-597.
  • 8Tamamura H, Hori A, Kanzaki N, et al. T140 analogs as CXCR4 antagonists identified as anti-metastatic agents in the treatment of breast cancer. FEBS Lett, 2003, 550(123): 79-83.
  • 9Tavazoie SF, Alarcon C, Oskarsson T, et al. Endogenous human microRNAs that suppress breast cancer metastasis. Nature, 2008, 451 (7175): 147-152.
  • 10Libura J, Drukala J, Majka M, et al. CXCR4-SDF-1 signaling is active in rhabdomyosarcoma cells and regulates locomotion, chemotaxis , and adhesion. Blood, 2002, 100(7): 2597-2606.

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