E-cadherin promoter polymorphisms are not associated with the aggressiveness of prostate cancer in Caucasian patients

被引:3
|
作者
Li, He-Cheng
Albert, Jeffrey M.
Shinohara, Eric T.
Cai, Qiuyin
Freyer, Andrea
Cai, Hui
Cao, Carolyn
Wang, Zuofei
Kataoka, Nobuhiko
Teng, Ming
Zheng, Wei
Lu, Bo [1 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Radiat Oncol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Vanderbilt Ingram Canc Ctr, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Sch Med, Dept Med, Nashville, TN 37232 USA
关键词
prostate cancer; E-cadherin; promoter; polymorphism; aggressiveness;
D O I
10.1016/j.urolonc.2006.02.018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: -160C -> A and -347G -> GA polymorphisms in the promoter region decrease E-cadherin gene transcription. Decreased E-cadherin expression predicts poor outcome among patients with cancer. We sought to investigate whether -160C -> A and/or -347G -> GA polymorphisms were associated with the aggressiveness of prostate cancer. Methods: TaqMan single nucleotide polymorphism genotyping assay (Applied Biosystems, Foster City, CA) was used to detect -160C -> A and -347G -> GA polymorphisms in deoxyribonucleic acid from the paraffin-embedded prostate tissues of 98 Caucasian patients. Results: The genotype frequencies were -160C/C: 48% (47 of 98); -160C/A: 44% (43 of 98); -160A/A: 8% (8 of 98); -347G/G: 68% (67 of 98); -347G/GA: 28% (27 of 98); and -347GA/GA: 4% (4 of 98). Using the chi-square test, we found that the polymorphisms -160C -> A and -347G -> GA were not related to other clinical and pathologic parameters (i.e., age, prostate-specific antigen level, Gleason grade, and clinical stage) (P > 0.05). In combination analysis, there was no significant relationship between patients with both -160C/C and -347G/G, and these same parameters (P > 0.05). Using the log-rank test, we found no significant difference in relapse-free survival and overall survival between patients with -160C/C and those with -160A/C or -160A/A (P = 0.0764 and 0.2746, respectively), and also no significant difference between patients with -347G/G and those with -347GA/G or -347GA/GA (P = 0.9416 and 0.7367, respectively). There was also no significant difference in relapse-free survival and overall survival between patients with homozygosities of -160C/-347G and patients with other genotypes (P = 0.1418 and 0.2434, respectively). Conclusion: We conclude that E-cadherin -160C -> A and/or -347G -> GA polymorphisms are not associated with the aggressiveness of prostate cancer in Caucasian patients. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:496 / 502
页数:7
相关论文
共 50 条
  • [41] Promoter polymorphisms of the PCA3 gene are not associated with its overexpression in prostate cancer patients
    Arambula-Meraz, Eliakym
    Irigoyen-Arredondo, Martin
    Cedano-Prieto, Dora
    Romo-Martinez, Enrique
    Luque-Ortega, Fred
    Picos-Cardenas, Veronica
    Alvarez-Arrazola, Marco
    Garcia-Magallanes, Noemi
    JOURNAL OF GENETICS, 2020, 99 (01)
  • [42] Therapeutic targets associated to E-cadherin dysfunction in gastric cancer
    Carneiro, Patricia
    Figueiredo, Joana
    Bordeira-Carrico, Renata
    Fernandes, Maria Sofia
    Carvalho, Joana
    Oliveira, Carla
    Seruca, Raquel
    EXPERT OPINION ON THERAPEUTIC TARGETS, 2013, 17 (10) : 1187 - 1201
  • [43] The E-cadherin repressor Snail is associated with lower overall survival of ovarian cancer patients
    K Blechschmidt
    S Sassen
    B Schmalfeldt
    T Schuster
    H Höfler
    K-F Becker
    British Journal of Cancer, 2008, 98 : 489 - 495
  • [44] Establishment and Validation of a Fluorescent Tracer System Based on E-cadherin Promoter
    Tan Y.
    Wu D.
    Yu L.
    Chen Y.
    Hunan Daxue Xuebao/Journal of Hunan University Natural Sciences, 2020, 47 (12): : 131 - 136
  • [45] Unmethylated E-Cadherin Gene Expression is Significantly Associated With Metastatic Human Prostate Cancer Cells in Bone
    Saha, Baisakhi
    Kaur, Pavinder
    Tsao-Wei, Denice
    Naritoku, Wesley Y.
    Groshen, Susan
    Datar, Ram H.
    Jones, Lawrence W.
    Imam, S. Ashraf
    PROSTATE, 2008, 68 (15) : 1681 - 1688
  • [46] Plasma levels of E-cadherin and MMP-13 in prostate cancer patients: correlation with PSA, testosterone and pathological parameters
    Bonaldi, Carolina M.
    Azzalis, Ligia A.
    Junqueira, Virginia B. C.
    de Oliveira, Claudia G. B.
    Boas, Viviane A. Vilas
    Gascon, Thas M.
    Gehrke, Flvia S.
    Kuniyoshi, Renata K.
    Alves, Beatriz C. A.
    Fonseca, Fernando L. A.
    TUMORI, 2015, 101 (02) : 185 - 188
  • [47] A single nucleotide polymorphism in the E-cadherin gene promoter-160 is not associated with risk of Korean gastric cancer
    Park, WS
    Cho, YG
    Park, JY
    Kim, CJ
    Lee, JH
    Kim, HS
    Lee, JW
    Song, YH
    Park, CH
    Park, YK
    Kim, SY
    Nam, SW
    Lee, SH
    Yoo, NJ
    Lee, JY
    JOURNAL OF KOREAN MEDICAL SCIENCE, 2003, 18 (04) : 501 - 504
  • [48] The E-cadherin repressor Snail is associated with lower overall survival of ovarian cancer patients
    Blechschmidt, K.
    Sassen, S.
    Schmalfeldt, B.
    Schuster, T.
    Hoefler, H.
    Becker, K-F
    BRITISH JOURNAL OF CANCER, 2008, 98 (02) : 489 - 495
  • [49] E-cadherin and metalloproteinase-1 and-7 polymorphisms in colorectal cancer
    de Lima, Jacqueline Miranda
    de Souza, Lessileia Gomes
    Cotrim Guerreiro da Silva, Ismael Dale
    Forones, Nora Manoukian
    INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS, 2009, 24 (02) : 99 - 106
  • [50] Down-regulation of E-cadherin enhances prostate cancer chemoresistance via Notch signaling
    Wenchu Wang
    Lihui Wang
    Atsushi Mizokami
    Junlin Shi
    Chunlin Zou
    Jinlu Dai
    Evan TKeller
    Yi Lu
    Jian Zhang
    ChineseJournalofCancer, 2017, 36 (03) : 150 - 162