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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Kim, Young-Jung Kim, Tae-Won Park, So-Ra Kim, Hyun-Tae Ryu, Si-Yun Jung, Ju-Young |
| Description | Author Affiliation: Kim YJ ( Department of Veterinary Medicine & Institute of Veterinary Science, Chungnam National University, 99 Daehak-ro, Yusung-gu, Daejeon 305-764, Republic of Korea.); Kim TW ( Department of Veterinary Medicine & Institute of Veterinary Science, Chungnam National University, 99 Daehak-ro, Yusung-gu, Daejeon 305-764, Republic of Korea.); Park SR ( Department of Veterinary Medicine & Institute of Veterinary Science, Chungnam National University, 99 Daehak-ro, Yusung-gu, Daejeon 305-764, Republic of Korea.); Kim HT ( Department of Veterinary Medicine & Institute of Veterinary Science, Chungnam National University, 99 Daehak-ro, Yusung-gu, Daejeon 305-764, Republic of Korea.); Ryu SY ( Department of Veterinary Medicine & Institute of Veterinary Science, Chungnam National University, 99 Daehak-ro, Yusung-gu, Daejeon 305-764, Republic of Korea.); Jung JY ( Department of Veterinary Medicine & Institute of Veterinary Science, Chungnam National University, 99 Daehak-ro, Yusung-gu, Daejeon 305-764, Republic of Korea. Electronic address: jyjung@cnu.ac.kr.) |
| Abstract | The aim of this study was to explore whether the Mre11, Rad50, and Nbs1 (MRN) complex is associated with DNA repair mechanisms in cisplatin-induced acute renal failure. Rats were randomly allocated into three groups: control, sacrificed 5 days (5D), and 10 days (10D) after 5mg/kg of cisplatin injection. The 5D group showed disrupted renal function together with enhanced MRN complex- and DNA repair-related protein expression. Meanwhile, in the 10D group, recovery from cisplatin-induced damage was accompanied by the reduced MRN expression, although the expression was still distinctive in proximal tubular cells and higher than the control group. Moreover, pretreatment with mirin, an MRN complex inhibitor, decreased cell viability and inhibited proliferating cell nuclear antigen expression in cisplatin-treated human embryonic kidney 293 cells. Taken together, cisplatin treatment could trigger the MRN complex expression in the kidney and inhibition of the complex might aggravate damage recovery processes. |
| File Format | HTM / HTML |
| ISSN | 13826689 |
| Issue Number | 1 |
| Volume Number | 40 |
| e-ISSN | 18727077 |
| Journal | Environmental Toxicology and Pharmacology |
| Language | English |
| Publisher | Elsevier |
| Publisher Date | 2015-07-01 |
| Publisher Place | Netherlands |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Discipline Environmental Health Discipline Pharmacology Antineoplastic Agents Toxicity Cisplatin Dna Repair Enzymes Metabolism Dna-binding Proteins Nuclear Proteins Animals Male Random Allocation Rats Rats, Sprague-dawley Journal Article Research Support, Non-u.s. Gov't |
| Content Type | Text |
| Resource Type | Article |
| Subject | Health, Toxicology and Mutagenesis Medicine Toxicology Pharmacology |
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