Human Papillomavirus 16 E7 DNA and E7 Protein Expression in Chinese Colorectal Carcinoma Patients

被引:0
作者
Zhang, Jian Cheng [1 ]
Wu, Gang [1 ]
Sun, PeiChun [1 ]
Kang, Yi [1 ]
Li, HongGuang [1 ]
Zhai, Bao Ping [1 ]
Zhu, Yuan Zeng [1 ]
Ding, Yi [2 ]
机构
[1] Henan Prov Hosp, Dept Gen Surg, Zhengzhou 450003, Henan, Peoples R China
[2] Weifang Med Univ, Dept Pathophysiol, Weifang 261053, Shandong, Peoples R China
来源
LIFE SCIENCE JOURNAL-ACTA ZHENGZHOU UNIVERSITY OVERSEAS EDITION | 2012年 / 9卷 / 03期
关键词
colorectal neoplasms; human papillomavirus (HPV); E7; oncogene; POLYMERASE-CHAIN-REACTION; SQUAMOUS-CELL CARCINOMA; CANCER; COLON; VIRUS;
D O I
暂无
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background The relationship between Human papillomavirus (HPV) 16 infection and the natural course of colorectal adenocarcinoma has not been fully defined. In this study, to investigate the correlation between HPV 16 infection and colorectal carcinoma HPV 16 E7 DNA and E7 protein were observed in 106 patients with primary colorectal adenocarcinoma. Material and methods 106 patients with primary colorectal adenocarcinoma were enrolled in this study. Fresh tissues were taken from both the tumors and the adjacent normal area of each patient. HPV16 E7 DNA and E7 protein were detected using polymerase chain reaction (PCR) and immunohistochemistry (IHC). Results HPV16 E7 expression was significantly higher in colorectal carcinoma (48/106) than that in adjacent normal mucosa (7/106)(P<0.001). A correlation was found between HPV16 E7 mRNA expression and tumor locations, 4/17 in the ascending colon carcinoma and 25/42 in the rectal carcinoma (P<0.05). Higher HPV16 E7 mRNA expression was also associated with lower Dukes stages(Dukes stages between A and C, P<0.05). IHC shows HPV16 E7 oncoprotein expressed in the nucleus of both tumor and normal mucosal cells. There was a correlation between the expression of E7 oncoprotein and E7 gene. Conclusions Our findings indicated that there was a correlation between colorectal adenocarcinoma and HPV 16 infection. HPV16 infection was relatively higher in the colorectal carcinoma and rare in the adjacent normal mucosa. Specimens expressing higher levels of HPV 16 E7 DNA were associated with lower Dukes stages and more distal locations. [Jian Cheng Zhang, Gang Wu, PeiChun Sun, Yi Kang, HongGuang Li, Bao Ping Zhai, Yuan Zeng Zhu, Yi Ding. Human Papillomavirus 16 E7 DNA and E7 Protein Expression in Chinese Colorectal Carcinoma Patients. Life Sci J 2012; 9(3): 2419-2423] (ISSN: 1097-8135). http://www.lifesciencesite.com.348
引用
收藏
页码:2419 / 2423
页数:5
相关论文
共 19 条
  • [1] REMOVAL OF INHIBITOR(S) OF THE POLYMERASE CHAIN-REACTION FROM FORMALIN FIXED, PARAFFIN WAX EMBEDDED TISSUES
    AN, SF
    FLEMING, KA
    [J]. JOURNAL OF CLINICAL PATHOLOGY, 1991, 44 (11) : 924 - 927
  • [2] Does human papilloma virus have a role in squamous cell carcinoma of the colon and upper rectum?
    Audeau, A
    Han, HW
    Johnston, MJ
    Whitehead, MW
    Frizelle, FA
    [J]. EUROPEAN JOURNAL OF SURGICAL ONCOLOGY, 2002, 28 (06): : 657 - 660
  • [3] The viral etiology of cervical cancer
    Bosch, FX
    Muñoz, N
    [J]. VIRUS RESEARCH, 2002, 89 (02) : 183 - 190
  • [4] Burnett-Hartman A. N., CANC EPIDEMIOL BIOMA, V20, P2288
  • [5] DETECTION OF HUMAN PAPILLOMAVIRUS DNA IN COLORECTAL CARCINOMAS BY POLYMERASE CHAIN-REACTION
    CHENG, JY
    SHEU, LF
    MENG, CL
    LEE, WH
    LIN, JC
    [J]. GUT, 1995, 37 (01) : 87 - 90
  • [6] HUMAN PAPILLOMAVIRUS 16 DNA IN NIH3T3 CELLS TRANSFORMED BY COLONIC-CANCER CELLULAR DNA
    CHENG, JY
    MENG, CL
    CHAO, CF
    GAU, SD
    LIN, JC
    [J]. GUT, 1993, 34 (12) : 1710 - 1713
  • [7] Ding Yi, 2005, Sheng Wu Yi Xue Gong Cheng Xue Za Zhi, V22, P778
  • [8] Frisch M, 1999, CANCER RES, V59, P753
  • [9] Sexually transmitted infection as a cause of anal cancer
    Frisch, M
    Glimelius, B
    vandenBrule, AJC
    Wohlfahrt, J
    Meijer, CJLM
    Walboomers, JMM
    Goldman, S
    Svensson, C
    Adami, HO
    Melbye, M
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (19) : 1350 - 1358
  • [10] Kessis TD, 1996, ONCOGENE, V13, P427