scholarly journals Prognostic value and clinicopathological significance of proliferating cell nuclear antigen expression in gastric cancer: a systematic review and meta-analysis

2017 ◽  
Vol Volume 10 ◽  
pp. 319-327 ◽  
Author(s):  
Songcheng Yin ◽  
Zhan Li ◽  
Jinyu Huang ◽  
Zhifeng Miao ◽  
Junyan Zhang ◽  
...  
Keyword(s):  
Gastric Cancer ◽  
Systematic Review ◽  
Proliferating Cell Nuclear Antigen ◽  
Prognostic Value ◽  
Meta Analysis ◽  
Antigen Expression ◽  
Nuclear Antigen ◽  
Clinicopathological Significance ◽  
Proliferating Cell

Prognostic Value of p53 and Proliferating Cell Nuclear Antigen Expression in Endometrial Carcinoma

1996 ◽  
Vol 62 (2) ◽  
pp. 192-198 ◽  
Author(s):  
Nicholas W. Hamel ◽  
Thomas J. Sebo ◽  
Timothy O. Wilson ◽  
Gary L. Keeney ◽  
Patrick C. Roche ◽  
...  
Keyword(s):  
Endometrial Carcinoma ◽  
Proliferating Cell Nuclear Antigen ◽  
Prognostic Value ◽  
Antigen Expression ◽  
Nuclear Antigen ◽  
Proliferating Cell

scholarly journals The prognostic value of proliferating cell nuclear antigen expression in colorectal cancer

Medicine ◽  
2018 ◽  
Vol 97 (50) ◽  
pp. e13752 ◽  
Author(s):  
He Zhou ◽  
Tao Huang ◽  
Yongfu Xiong ◽  
Linglong Peng ◽  
Rong Wang ◽  
...  
Keyword(s):  
Colorectal Cancer ◽  
Proliferating Cell Nuclear Antigen ◽  
Prognostic Value ◽  
Antigen Expression ◽  
Nuclear Antigen ◽  
Proliferating Cell

Prognostic Value of DNA Ploidy and Proliferating Cell Nuclear Antigen in Gastric Cancer

Oncology ◽  
1998 ◽  
Vol 55 (4) ◽  
pp. 300-306 ◽  
Author(s):  
Kazuo Hirose ◽  
Atsushi Iida ◽  
Akio Yamaguchi ◽  
Hidetoshi Onchi ◽  
Hirofumi Awata ◽  
...  
Keyword(s):  
Gastric Cancer ◽  
Proliferating Cell Nuclear Antigen ◽  
Prognostic Value ◽  
Dna Ploidy ◽  
Nuclear Antigen ◽  
Proliferating Cell

The Impact of 5-Azacytidine on Placental Weight, Glycoprotein Pattern and Proliferating Cell Nuclear Antigen Expression in Rat Placenta

Placenta ◽  
2007 ◽  
Vol 28 (8-9) ◽  
pp. 803-811 ◽  
Author(s):  
L. Šerman ◽  
M. Vlahović ◽  
M. Šijan ◽  
F. Bulić-Jakuš ◽  
A. Šerman ◽  
...  
Keyword(s):  
Proliferating Cell Nuclear Antigen ◽  
Antigen Expression ◽  
Placental Weight ◽  
Nuclear Antigen ◽  
The Impact ◽  
Proliferating Cell

scholarly journals An evaluation of antioxidant effects on recovery from postischemic acute renal failure.

1994 ◽  
Vol 4 (8) ◽  
pp. 1588-1597
Author(s):  
R A Zager ◽  
S M Fuerstenberg ◽  
P H Baehr ◽  
D Myerson ◽  
B Torok-Storb
Keyword(s):  
Renal Failure ◽  
Acute Renal Failure ◽  
Dna Fragmentation ◽  
Proliferating Cell Nuclear Antigen ◽  
Antigen Expression ◽  
Nuclear Antigen ◽  
Terminal Deoxynucleotidyl Transferase ◽  
Tubular Necrosis ◽  
Proliferating Cell

Xanthine oxidase (XO) activity and hydroxyl radical (.OH) formation are widely proposed mediators of renal reperfusion injury, potentially altering the severity of, and recovery from, postischemic acute renal failure. The goal of this study was to ascertain whether combination XO inhibitor (oxypurinol) and .OH scavenger (Na benzoate) therapy, given at the time of renal ischemia, alters the extent of: (1) tubular necrosis and filtration failure; (2) DNA fragmentation/apoptosis (assessed in situ by terminal deoxynucleotidyl transferase reactivity); (3) early tubular regenerative responses (proliferating cell nuclear antigen expression; (3H)thymidine incorporation); and (4) the rate and/or degree of functional and morphologic repair. The effects of XO inhibition, .OH scavengers, and "catalytic" iron (FeSO4) on human proximal tubular cell proliferation in vitro were also assessed with a newly established cell line (HK-2). Male Sprague-Dawley rats were subjected to 35 min of bilateral renal arterial occlusion with or without oxypurinol/benzoate therapy. These agents did not alter the extent of tubular necrosis or filtration failure, proliferating cell nuclear antigen expression or thymidine incorporation, or the rate/extent of renal functional/morphologic repair. DNA fragmentation did not precede tubular necrosis, and it was unaffected by antioxidant therapy. By 5 days postischemia, both treatment groups demonstrated regenerating epithelial fronds that protruded into the lumina. These structures contained terminal deoxynucleotidyl transferase-reactive, but morphologically intact, cells, suggesting the presence of apoptosis. Oxypurinol and .OH scavengers (benzoate; dimethylthiourea) suppressed in vitro tubular cell proliferation; conversely, catalytic Fe had a growth-stimulatory effect. These results suggest that: (1) XO inhibition/.OH scavenger therapy has no discernible net effect on postischemic acute renal failure; (2) DNA fragmentation does not precede tubular necrosis, suggesting that it is not a primary mediator of ischemic cell death; and (3) antioxidants can be antiproliferative for human tubular cells, possibly mitigating their potential beneficial effects.

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