Article ; Online: Decreased prolyl hydroxylase 3 mRNA expression in oncocytomas compared with clear cell renal cell carcinoma.
The International journal of biological markers
2020 Volume 35, Issue 4, Page(s) 80–86
Abstract: Introduction: Hypoxia inducible factors (HIF) and prolyl hydroxylase domain (PHD) enzymes play a central role in tumor progression in clear cell renal cell carcinoma (ccRCC). However, there are currently no data regarding the behavior of this pathway ( ... ...
Abstract | Introduction: Hypoxia inducible factors (HIF) and prolyl hydroxylase domain (PHD) enzymes play a central role in tumor progression in clear cell renal cell carcinoma (ccRCC). However, there are currently no data regarding the behavior of this pathway (HIF/PHD) in a large number of benign renal tumors, the oncocytomas. The aim of the present study was to compare the expression levels of these factors between ccRCC and oncocytoma tumors. Material and methods: A total of 56 fresh frozen specimens from patients with ccRCC and 14 oncocytoma specimens were analyzed via reverse transcription-quantitative polymerase chain reaction in order to assess the expression levels of HIF-1α, HIF-2α, PHD1, PHD2, and PHD3. The analysis involved both fresh frozen tumor samples as well as adjacent normal kidney tissues. Results: In ccRCC, HIF-1α and HIF-2α levels were upregulated in 65.5% and 71.4% of cases, respectively. PHD3 was downregulated only in 15.4% of the ccRCC cases, in contrast with oncocytoma cases, which exhibited low expression levels in the majority. The upregulation of PHD3 messenger RNA (mRNA) levels in ccRCC when compared with oncocytoma was statistically significant ( Conclusion: To the best of our knowledge, this is the first time that the HIF/PHD pathway was compared between ccRCC and a common benign tumor, identifying the upregulation of PHD3 as the possible underlying factor guiding the difference in the behavior of ccRCC. |
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MeSH term(s) | Adenoma, Oxyphilic/genetics ; Adenoma, Oxyphilic/metabolism ; Adult ; Aged ; Aged, 80 and over ; Basic Helix-Loop-Helix Transcription Factors/biosynthesis ; Basic Helix-Loop-Helix Transcription Factors/genetics ; Carcinoma, Renal Cell/genetics ; Carcinoma, Renal Cell/metabolism ; Female ; Humans ; Hypoxia-Inducible Factor 1, alpha Subunit/biosynthesis ; Hypoxia-Inducible Factor 1, alpha Subunit/genetics ; Hypoxia-Inducible Factor-Proline Dioxygenases/genetics ; Hypoxia-Inducible Factor-Proline Dioxygenases/metabolism ; Kidney Neoplasms/genetics ; Kidney Neoplasms/metabolism ; Male ; Middle Aged ; Prolyl Hydroxylases/genetics ; Prolyl Hydroxylases/metabolism ; Prospective Studies ; RNA, Messenger/biosynthesis ; RNA, Messenger/genetics ; RNA, Messenger/metabolism |
Chemical Substances | Basic Helix-Loop-Helix Transcription Factors ; HIF1A protein, human ; Hypoxia-Inducible Factor 1, alpha Subunit ; RNA, Messenger ; endothelial PAS domain-containing protein 1 (1B37H0967P) ; Prolyl Hydroxylases (EC 1.14.11.-) ; EGLN3 protein, human (EC 1.14.11.29) ; Hypoxia-Inducible Factor-Proline Dioxygenases (EC 1.14.11.29) |
Language | English |
Publishing date | 2020-10-29 |
Publishing country | United States |
Document type | Journal Article |
ZDB-ID | 645113-5 |
ISSN | 1724-6008 ; 0393-6155 |
ISSN (online) | 1724-6008 |
ISSN | 0393-6155 |
DOI | 10.1177/1724600820960478 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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