Overexpression of endoplasmic reticulum molecular chaperone GRP94 and GRP78 in human lung cancer tissues and its significance

被引:160
|
作者
Wang, Q [1 ]
He, ZZ
Zhang, JH
Wang, YY
Wang, T
Tong, SP
Wang, LJ
Wang, SJ
Chen, YH
机构
[1] Dalian Med Univ, Hosp 2, Dept Resp, Dalian 116023, Peoples R China
[2] Dalian Med Univ, Hosp 1, Dept Urinary Surg, Dalian 116027, Peoples R China
[3] Dalian Med Univ, Dept Postgrad, Dalian, Peoples R China
[4] China Med Univ, Dept Dev Biol, Shenyang 110001, Peoples R China
来源
CANCER DETECTION AND PREVENTION | 2005年 / 29卷 / 06期
基金
中国国家自然科学基金;
关键词
Grp94; GRP78; expression; human lung cancer; endoplasmic reticulum molecular chaperone; differentiation; cancer progression; RNA isolation; immunohistochemistry; Western blot; lung squamous carcinoma; lung adenocarcinoma; lung adenosquamous carcinom; lung small cell carcinoma; lung giant cell carcinoma;
D O I
10.1016/j.cdp.2005.09.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: To investigate the relationship between the expression of glucose-regulated protein94 (GRP94) and GRP78 at the level of mRNA and protein in vivo and in human lung cancer. Methods: RT-PCR, real-time PCR, immunohistochemistry and/or Western blot were used in 54 cases of lung cancer and corresponding normal lung tissue. Results: The expression pattern of GRP94 and GRP78 was similar. There was a significant overexpression of GRP94 and GRP78 at both mRNA and protein levels in cancer tissues as compared to normal tissues. The relative levels of GRP94 and GRP78 mRNA evaluated by RT-PCR in cancer and normal lung tissue were: GRP94: 3.48 +/- 2.06 versus 2.01 +/- 1.83; GRP78: 3.64 +/- 1.87 versus 2.21 +/- 1.54; by real-time PCR were: GRP94: 2.89 +/- 0.64 versus 1.12 +/- 0.54; GRP78: 2.56 +/- 0.82 versus 0.96 +/- 0.42. The relative level of GRP94 and GRP78 protein by Western blot in cancer and normal lung tissue were: GRP94: 3.46 +/- 1.72 versus 1.81 +/- 0.92; GRP78: 4.84 +/- 2.55 versus 1.91 +/- 1.15, indicating an approximate 2-fold and a 3-fold increase in GRP94 and GRP78 protein in cancer tissue as compared with normal tissue. Immunohistochemistry result for GRP94 and GRP78 in cancer and normal tissue was similar, that is: a stronger stain was observed in cancer tissue (main intensity of staining ++ to +++) compared to normal tissue (main intensity of staining + to ++). All the difference for GRP94 and GRP78 between the two tissues were significant (p < 0.05). Furthermore, the overexpression of GRP94 and GRP78 in the cancer tissue correlated with grade of differentiation and stage of tumors. There was stronger expression in poorly differentiated tumors than in well-moderately differentiated tumors (p < 0.05). There was also stronger expression in stage III than in stages I and II tumors (p < 0.05). No statistically significant differences were found among various pathologic types of tumors. Correlation analysis showed that there is a positive correlation between GRP94 and GRP78. Conclusion: The expression pattern of GRP94 and GRP78 was similar in human lung cancer. They both were related with the differentiation and progression of the cancer. The expression at mRNA and protein level may be valuable in evaluating the grade of differentiation and clinical stage of human lung cancer. (c) 2005 International Society for Preventive Oncology. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:544 / 551
页数:8
相关论文
共 50 条
  • [1] Expression of endoplasmic reticulum molecular chaperone Grp78 in human lung cancer and its clinical significance
    Uramoto, H
    Sugio, K
    Oyama, T
    Nakata, S
    Ono, K
    Yoshimastu, T
    Morita, M
    Yasumoto, K
    [J]. LUNG CANCER, 2005, 49 (01) : 55 - 62
  • [2] Expression of endoplasmic reticulum molecular chaperon GRP94 in human lung cancer tissues and its clinical significance
    Wang, Q
    An, LJ
    Chen, YH
    Yue, SC
    [J]. CHINESE MEDICAL JOURNAL, 2002, 115 (11) : 1615 - 1619
  • [3] Overexpression of GRP78 and GRP94 is involved in colorectal carcinogenesis
    Takahashi, Hiroyuki
    Wang, Jian-ping
    Zheng, Hua-chuan
    Masuda, Shinji
    Takano, Yasuo
    [J]. HISTOLOGY AND HISTOPATHOLOGY, 2011, 26 (06) : 663 - 671
  • [4] Grp78, Grp94, and Grp170 interact with α1-antitrypsin mutants that are retained in the endoplasmic reticulum
    Schmidt, BZ
    Perlmutter, DH
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2005, 289 (03): : G444 - G455
  • [6] Expression and clinical significance of glucose regulated proteins GRP78 and GRP94 in human colon cancer
    Liu, Ming-hua
    Wang, Meng-chun
    Gao, Na
    Li, Yan
    Jiang, Wei-guo
    [J]. CHINESE JOURNAL OF CANCER RESEARCH, 2010, 22 (01) : 42 - 48
  • [7] Autoimmunity to endoplasmic reticulum chaperone GRP94 in myasthenia gravis
    Suzuki, Shigeaki
    Utsugisawa, Kimiaki
    Iwasa, Kazuo
    Satoh, Takashi
    Nagane, Yuriko
    Yoshikawa, Hiroaki
    Kuwana, Masataka
    Suzuki, Norihiro
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 2011, 237 (1-2) : 87 - 92
  • [8] The endoplasmic reticulum chaperone GRP94 is induced in the thyrocytes by cadmium
    Kwon, OY
    Kim, YJ
    Choi, YM
    Kim, H
    Song, C
    Shong, MH
    [J]. ZEITSCHRIFT FUR NATURFORSCHUNG C-A JOURNAL OF BIOSCIENCES, 1999, 54 (7-8): : 573 - 577
  • [9] GRP78: A chaperone with diverse roles beyond the endoplasmic reticulum
    Quinones, Quintin J.
    de Ridder, Gustaaf G.
    Pizzo, Salvatore V.
    [J]. HISTOLOGY AND HISTOPATHOLOGY, 2008, 23 (11) : 1409 - 1416
  • [10] Induction of GRP78/GRP94 Expression Inhibits TLR4-Induced Endoplasmic Reticulum Stress (ERS)
    Coope, Andressa
    Velloso, Licio A.
    [J]. DIABETES, 2011, 60 : A403 - A403