Loss of retinoic acid receptor-β expression is an early event during esophageal carcinogenesis

被引:101
作者
Qiu, HM
Zhang, W
El-Naggar, AK
Lippman, SM
Lin, PZ
Lotan, R
Xu, XC
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Clin Canc Prevent, 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 Pathol, Houston, TX 77030 USA
[4] Chinese Acad Med Sci, Ctr Lab Tumor Biol, Canc Inst & Hosp, Beijing 100037, Peoples R China
关键词
D O I
10.1016/S0002-9440(10)65467-3
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
We recently observed that growth inhibition of esophageal cancer cells by retinoic acid (RA) was associated with both constitutive expression and RA-induced up-regulation of RA receptor beta (RAR-beta). Cell lines that did not express RAR-beta were also resistant to RA. To explore the expression of RAR-beta mRNA in vivo, we analyzed esophageal tissue specimens from 16 normal mucosae, 30 dysplastic lesions, and 157 esophageal tumors by in situ hybridization. RAR-beta was detected in 88% (14/16) of normal esophageal tissues and in 96% (96/100) of distant normal esophageal mucosa from cancer specimens. In contrast, RAR-beta was expressed in only 57% (17/30) of dysplastic lesions and in 54% (84/157) of carcinomas. Among esophageal carcinomas RAR-beta mRNA was expressed in 62% (26/42) of wed-differentiated, 54% (27/50) of moderately differentiated, and only 29% (4/14) of poorly differentiated SCCs. Our data suggest that the loss of RAR-beta expression is an early event associated with esophageal carcinogenesis and the status of squamous differentiation.
引用
收藏
页码:1519 / 1523
页数:5
相关论文
共 23 条
  • [1] Lung tumors in mice expressing an antisense RAR beta 2 transgene
    Berard, J
    Laboune, F
    Mukuna, M
    Masse, S
    Kothary, R
    Bradley, WEC
    [J]. FASEB JOURNAL, 1996, 10 (09) : 1091 - 1097
  • [2] NUTRITION INTERVENTION TRIALS IN LINXIAN, CHINA - SUPPLEMENTATION WITH SPECIFIC VITAMIN MINERAL COMBINATIONS, CANCER INCIDENCE, AND DISEASE-SPECIFIC MORTALITY IN THE GENERAL-POPULATION
    BLOT, WJ
    LI, JY
    TAYLOR, PR
    GUO, WD
    DAWSEY, S
    WANG, GQ
    YANG, CS
    ZHENG, SF
    GAIL, M
    LI, GY
    YU, Y
    LIU, BQ
    TANGREA, J
    SUN, YH
    LIU, FS
    FRAUMENI, JF
    ZHANG, YH
    LI, B
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (18): : 1483 - 1492
  • [3] A decade of molecular biology of retinoic acid receptors
    Chambon, P
    [J]. FASEB JOURNAL, 1996, 10 (09) : 940 - 954
  • [4] Altered retinoic acid receptors
    deThe, H
    [J]. FASEB JOURNAL, 1996, 10 (09) : 955 - 960
  • [5] Enzinger PG, 1999, CANCER, V85, P1213, DOI 10.1002/(SICI)1097-0142(19990315)85:6<1213::AID-CNCR1>3.0.CO
  • [6] 2-N
  • [7] GEBERT JF, 1991, ONCOGENE, V6, P1859
  • [8] HIGHLIGHTS OF THE CANCER CHEMOPREVENTION STUDIES IN CHINA
    HAN, J
    [J]. PREVENTIVE MEDICINE, 1993, 22 (05) : 712 - 722
  • [9] TUMOR-SUPPRESSIVE EFFECT OF THE RETINOIC ACID RECEPTOR-BETA IN HUMAN EPIDERMOID LUNG-CANCER CELLS
    HOULE, B
    ROCHETTEEGLY, C
    BRADLEY, WEC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (03) : 985 - 989
  • [10] HU L, 1991, CANCER RES, V51, P3972