Nuclear factor-κB (NF-κB) is frequently expressed in lung cancer and preneoplastic lesions

被引:174
作者
Tang, Ximing
Liu, Diane
Shishodia, Shishir
Ozburn, Natalie
Behrens, Carmen
Lee, J. Jack
Hong, Waun Ki
Aggarwal, Bharat B.
Wistuba, Ignacio I.
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Pathol, Unit 85, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
[3] Univ Texas, MD Anderson Canc Ctr, Dept Biostat & Appl Math, Houston, TX 77030 USA
[4] Univ Texas, MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77030 USA
关键词
NF-kappa B; lung cancer; inflammation; lung preneoplasia; squamous dysplasia; EGFR mutation; K-RAS mutation;
D O I
10.1002/cncr.22315
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. Nuclear factor-kappa B (NF-kappa B), a key transcription factor thought to play a major role in carcinogenesis, regulates many important signaling pathways involved in tumor promotion. Although NF-kappa B can be activated in lung cancer cell lines by tobacco exposure, there have been no studies of the expression of NF-kappa B in lung cancer pathogenesis. METHODS. The immunohistochemical expression of NF-kappa B p65 was investigated in 394 lung cancers (370 nonsmall cell lung carcinomas [NSCLC]; and 24 small cell lung carcinomas [SCLC]) and 269 lung normal epithelium and preneoplastic lesions, including hyperplasias, squamous metaplasias, dysplasias, and atypical adenomatous hyperplasias. RESULTS. High levels of nuclear immunohistochemical expression of NF-kappa B p65 were detected in the lung cancers, with significantly higher levels in SCLCs compared with NSCLCs (P <.0001). In adenocarcinomas the NF-kappa B p65 expression level was significantly higher in advanced TNM stages (III-IV) than in earlier stages (I-II) (P <.0001), and when NF-kappa B p65 is dichotomized using 50% as the cutoff point (high vs low), a higher NF-kappa B p65 expression level was detected in tumors having either K-RAS (P =.02) or EGFR (P =.009) mutations compared with wildtype tumors. A relatively high level of nuclear NF-kappa B p65 expression was detected in normal and mildly abnormal epithelium, and a progression with increasing histology severity was detected in preneoplastic lesions. CONCLUSIONS. NF-kappa B p65 nuclear expression is an early and frequent phenomenon in the pathogenesis of lung cancer. The findings indicate that NF-kappa B activation plays an important role in lung cancer pathogenesis and is a suitable target for the development of new lung cancer therapies and chemoprevention strategies.
引用
收藏
页码:2637 / 2646
页数:10
相关论文
共 49 条
  • [1] NF-κB activation in Esophageal adenocarcinoma -: Relationship to Barrett's metaplasia, survival, and response to neoadjuvant chemoradiotherapy
    Abdel-Latif, MMM
    O'Riordan, J
    Windle, HJ
    Carton, E
    Ravi, N
    Kelleher, D
    Reynolds, JV
    [J]. ANNALS OF SURGERY, 2004, 239 (04) : 491 - 500
  • [2] Molecular targets of dietary agents for prevention and therapy of cancer
    Aggarwal, BB
    Shishodia, S
    [J]. BIOCHEMICAL PHARMACOLOGY, 2006, 71 (10) : 1397 - 1421
  • [3] Nuclear factor-κ-B:: The enemy within
    Aggarwal, BB
    [J]. CANCER CELL, 2004, 6 (03) : 203 - 208
  • [4] Chemotherapy induces the expression of cyclooxygenase-2 in non-small cell lung cancer
    Altorki, NK
    Port, JL
    Zhang, F
    Golijanin, D
    Thaler, HT
    Duffield-Lillico, AJ
    Subbaramaiah, K
    Dannenberg, AJ
    [J]. CLINICAL CANCER RESEARCH, 2005, 11 (11) : 4191 - 4197
  • [5] Acquired somatic mutations in the molecular pathogenesis of COPD
    Anderson, GP
    Bozinovski, S
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2003, 24 (02) : 71 - 76
  • [6] Ballaz Santiago, 2003, Clin Lung Cancer, V5, P46, DOI 10.3816/CLC.2003.n.021
  • [7] Chemopreventive agents induce suppression of nuclear factor-κB leading to chemosensitization
    Bharti, AC
    Aggarwal, BB
    [J]. CELL SIGNALING, TRANSCRIPTION, AND TRANSLATION AS THERAPEUTIC TARGETS, 2002, 973 : 392 - 395
  • [8] Epidermal growth factor-induced nuclear factor κB activation:: A major pathway of cell-cycle progression in estrogen-receptor negative breast cancer cells
    Biswas, DK
    Cruz, AP
    Gansberger, E
    Pardee, AB
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) : 8542 - 8547
  • [9] Cassidy PB, 2002, CLIN CANCER RES, V8, P846
  • [10] Colby T V, 1998, Adv Anat Pathol, V5, P205, DOI 10.1097/00125480-199807000-00001