The role of connexins in prostate cancer promotion and progression

被引:60
作者
Czyz, Jaroslaw [1 ]
Szpak, Katarzyna [1 ]
Madeja, Zbigniew [1 ]
机构
[1] Jagiellonian Univ, Dept Cell Biol, Fac Biochem Biophys & Biotechnol, PL-30387 Krakow, Poland
关键词
GAP-JUNCTIONAL COMMUNICATION; RENAL-CELL CARCINOMA; SUICIDE GENE-THERAPY; STEM-CELLS; EPITHELIAL-CELLS; BREAST-CANCER; RAT PROSTATE; INTERCELLULAR COMMUNICATION; GLIOMA-CELLS; EXPRESSING CONNEXIN-43;
D O I
10.1038/nrurol.2012.14
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
100201 [内科学]; 100221 [泌尿外科学];
摘要
Prostate cancer is a prevalent disease that is characterized by a presumably long latency period and a moderate propensity to metastasize. Although a range of mechanisms have been implicated in prostate carcinogenesis, the factors determining the initiation of metastasis remain obscure. The synchronized function of prostate cells depends on their metabolic and electrical coupling; disturbance of these functions has long been suggested to be integral to prostate carcinogenesis. However, although connexins form intercellular channels involved in gap-junction-mediated intercellular coupling (GJIC), whether these proteins also have GJIC-independent roles in cancer progression and metastasis remains a matter of debate. Some data indicate a correlation between connexin expression and the invasive potential of prostate cancer cells, which points to stage-specific functions of connexins during prostate cancer development. For example, restoration of connexin expression seems to be crucial for the formation of invasive cell subsets within heterogeneous prostate cancer cell populations that have undergone aberrant differentiation. Consequently, the clinical application of therapeutic and prophylactic approaches focused on the modulation of connexin expression in prostate cancer cells should be reconsidered.
引用
收藏
页码:274 / 282
页数:9
相关论文
共 131 条
[1]
Visualization of Connexin 43-positive cells of glioma and the periglioma zone by means of intravenously injected monoclonal antibodies [J].
Baklaushev, Vladimir P. ;
Yusubalieva, Gaukhar M. ;
Tsitrin, Eugene B. ;
Gurina, Olga I. ;
Grinenko, Nadezhda Ph ;
Victorov, Ilya V. ;
Chekhonin, Vladimir P. .
DRUG DELIVERY, 2011, 18 (05) :331-337
[2]
Connexin43 enhances glioma invasion by a mechanism involving the carboxy terminus [J].
Bates, Dave C. ;
Sin, W. C. ;
Aftab, Q. ;
Naus, C. C. .
GLIA, 2007, 55 (15) :1554-1564
[3]
Prognostic value of connexin43 expression in patients with clinically localized prostate cancer [J].
Benko, G. ;
Spajic, B. ;
Demirovic, A. ;
Stimac, G. ;
Kruslin, B. ;
Tomas, D. .
PROSTATE CANCER AND PROSTATIC DISEASES, 2011, 14 (01) :90-95
[4]
MORPHOGENETIC ASPECTS OF NORMAL AND ABNORMAL PROSTATIC GROWTH [J].
BONKHOFF, H ;
REMBERGER, K .
PATHOLOGY RESEARCH AND PRACTICE, 1995, 191 (09) :833-835
[5]
Bonkhoff H, 1996, PROSTATE, V28, P98
[6]
Bonkhoff H, 1996, EUR UROL, V30, P201
[7]
Burra Sirisha, 2011, Int J Biochem Mol Biol, V2, P119
[8]
Dendritic processes of osteocytes are mechanotransducers that induce the opening of hemichannels [J].
Burra, Sirisha ;
Nicolella, Daniel P. ;
Francis, W. Loren ;
Freitas, Christopher J. ;
Mueschke, Nicholas J. ;
Poole, Kristin ;
Jiang, Jean X. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (31) :13648-13653
[9]
Carruba G, 2002, PROSTATE, V50, P73
[10]
Carruba G, 2002, ANN NY ACAD SCI, V963, P156