Advanced Search
CHEN Bin, LUO Rong-cheng, CHEN Jian-Peng, CHEN Xiao-Hua. Expression of EGFR Protein in Human Gastric Cancer and Its Clinical Value[J]. Cancer Research on Prevention and Treatment, 2008, 35(02): 113-115. DOI: 10.3971/j.issn.1000-8578.2048
Citation: CHEN Bin, LUO Rong-cheng, CHEN Jian-Peng, CHEN Xiao-Hua. Expression of EGFR Protein in Human Gastric Cancer and Its Clinical Value[J]. Cancer Research on Prevention and Treatment, 2008, 35(02): 113-115. DOI: 10.3971/j.issn.1000-8578.2048

Expression of EGFR Protein in Human Gastric Cancer and Its Clinical Value

More Information
  • Corresponding author:

    LUO Rongcheng

  • Received Date: March 04, 2007
  • Revised Date: July 09, 2007
  • Objective  To investigate the expression of EGFR in gastric cancer and its relationship with clinical pathologic characters, analyze the relationship between EGFR expression and survival time of gastric cancer, and discuss the feasibility of EGFR as prognostic markers and molecular target . Methods  The expression of EGFR in gastric cancer was studied by immunohistochemical technique with its relation to follow2up data. We analyzed its detect outcome with clinical pathologic characters. Results  ①The 44 of 103 gastric cancer specimens (42. 7 %) were positive for EGFR, and the expression of EGFR was not found in gastric normal tissue ; ②Their expression was not correlated with sex, age, size and site of tumor and degree of differentiation ( P > 0. 05) . The positive expression rates of EGFR was related to the depth of invasion, clinical stage, lymph node and distant metastasis of gastric cancer patients ( P < 0. 05) ; ③Median survival time of patients with EGFR positive is 11. 0 months. Median survival time of patient s with EGFR negative is 65. 2 months. There is statistical significe be2 tween median survival period of patients with EGFR positive and negative ( P < 0. 05) . Conclusion  ①The ex2 pression of EGFR was closely related to invasion, metastasis and prognosis of gastric cancer, and it could be used to evaluate the biological behaviors and prognosis of gastric cancer. ②High positive rate of EGFR expression in gastric cancer, provide a theoretical basis for application of molecular targeted drugs, such as IMC2C225, ZD1839 and OSI2774.
  • Related Articles

    [1]ZHANG Lin'gang, ZHANG Tianyu, TAN Ning, YAO Shihong, ZHANG Jianhua. Combined Application of Vitamin C and Arsenic Trioxide in Inhibiting Bladder Cancer Cell Lines T-24 in vitro[J]. Cancer Research on Prevention and Treatment, 2017, 44(2): 103-107. DOI: 10.3971/j.issn.1000-8578.2017.02.005
    [2]ZHANG Hemei, HE Jinjiang, GAO Siai, WEI Hong, ZHANG Zengli, TONG Jian, Tom K·Hei, LI Bingyan. TGFBI Inhibits Proliferation of Breast Cancer Cell in vitro and in vivo[J]. Cancer Research on Prevention and Treatment, 2014, 41(07): 693-697. DOI: 10.3971/j.issn.1000-8578.2014.07.001
    [3]ZHANG Zhen-hua, WU Jing-bo. Cytotoxicity Effect of Thermo-chemotherpy with Pegylated Liposomal Doxorubicin on Human Esophageal Carcinoma in vitro[J]. Cancer Research on Prevention and Treatment, 2011, 38(07): 736-739. DOI: 10.3971/j.issn.1000-8578.2011.07.002
    [4]Li Tai-yuan, ZHANG Hai-tao, DUANMU Jin-zhong. Exploration of Inhibitory Effect of Sandostain to Colorectal Cancer Cell in vitro[J]. Cancer Research on Prevention and Treatment, 2007, 34(12): 949-951. DOI: 10.3971/j.issn.1000-8578.52
    [5]LIU Ying-jie, MA Yuan-fang, LIU Guang-chao, WU Xiong-wen. Inhibitory Effects of Nimesulide on Proliferation of Human Small Cell Lung Cancer Cell Line NCL-H446[J]. Cancer Research on Prevention and Treatment, 2006, 33(06): 408-410,. DOI: 10.3971/j.issn.1000-8578.2877
    [6]ZHU Zu-an, LIU Ying, FEI Su-juan. Inhibitory Effects of Sulindac and Nimesulide on Cell Proliferation and COX-2, NF-κB Expression in Human Gastric Carcinoma Cell Line SGC-7901[J]. Cancer Research on Prevention and Treatment, 2005, 32(10): 623-625. DOI: 10.3971/j.issn.1000-8578.529
    [7]FAN Hai-tao, ZHU De-chun, ZHANG Ming, WANG Hai-jun, LIU Lu-cheng. Cyclooxygenase Inhibitor Suppressed COX-2 Expression and Induced Apoptosis in Human Bladder Cancer Cell Line T24[J]. Cancer Research on Prevention and Treatment, 2005, 32(07): 406-408. DOI: 10.3971/j.issn.1000-8578.826
    [8]CAO Zheng-guo, ZHOU Si-wei, XONG Xiao-dong, LUO Gang, LIU Ji-hong, YE Zhang-qun. Effect of Urinary Trypsin Inhibitor on the Expression of Urokinase-type Plasminogen Activator in Human Bladder Cancer Cell T24 in Vitro[J]. Cancer Research on Prevention and Treatment, 2004, 31(12): 754-755. DOI: 10.3971/j.issn.1000-8578.1590
    [9]WANG Shun-wen, GAO Qing. The Effects of Nimesulide on Cell Proliferation and on Induce Apoptosis in Human Carcinoma of the Esophagus Cells[J]. Cancer Research on Prevention and Treatment, 2004, 31(04): 208-210. DOI: 10.3971/j.issn.1000-8578.3213
    [10]YANG Si-xing, WEN Yan, ZHANG Xue-jun, et al, . Growth Inhibition and Apoptosis of Human Bladder Cancer Cell Line T24 Induced by All-Trans-Retinoic Acid[J]. Cancer Research on Prevention and Treatment, 2000, 27(05): 335-336. DOI: 10.3971/j.issn.1000-8578.2753

Catalog

    CHEN Xiao-Hua

    1. On this Site
    2. On Google Scholar
    3. On PubMed
    Article views (3007) PDF downloads (919) Cited by()

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return