Detection of the Kidney Tumor Suppressor DUSP9 in the Urine of Healthy Donors

The DUSP9/MKP-4 belongs to the family of bispecific protein phosphatases that negatively regulate MAP kinases (ERK, p38 and JNK). The expression of DUSP9 is significantly (20-80-fold) reduced compared to normal tissue in 95% of the studied human renal cell carcinoma samples. These and other scientific data indicate that DUSP9 is an attractive target for the use in clinical practice. However, so far, postoperative tumor biopsy samples remain the only source of clinical material in which expression of DUSP9 has been studied.. This significantly limits the possibilities of using DUSP9 for clinical purposes. The purpose of this work was to find out whether it would be possible to detect DUSP9 in human urine. In the study we used human kidney carcinoma ACHN cells transfected with a vector, expressing DUSP9 and urine samples from 3 healthy volunteers. DUSP9 protein was detected by the Western blot method in precipitates obtained by centrifugation. We have shown that the DUSP9 protein is present in the pellet of the urine fraction obtained by low-speed centrifugation (10000 g). It is also present in the fraction of extracellular vesicles enriched with exosomes. The obtained result indicates that the analysis of DUSP9 expression is possible using a liquid biopsy, which, in turn, can significantly expand the applicability of this analysis for clinical purposes.

Authors

Institutions

Publication Details

Journal
Biomedical Chemistry Research and Methods
Published
2025-01-01
DOI
https://doi.org/10.18097/bmcrm00267
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Detection of the Kidney Tumor Suppressor DUSP9 in the Urine of Healthy Donors

Anya Polischouk, В И Евтушенко, E. I. Yakubovich
Biomedical Chemistry Research and Methods
Extracellular vesicles in disease
article

Detection of the Kidney Tumor Suppressor DUSP9 in the Urine of Healthy Donors

Anya Polischouk, В И Евтушенко, E. I. Yakubovich
article en

Abstract

The DUSP9/MKP-4 belongs to the family of bispecific protein phosphatases that negatively regulate MAP kinases (ERK, p38 and JNK). The expression of DUSP9 is significantly (20-80-fold) reduced compared to normal tissue in 95% of the studied human renal cell carcinoma samples. These and other scientific data indicate that DUSP9 is an attractive target for the use in clinical practice. However, so far, postoperative tumor biopsy samples remain the only source of clinical material in which expression of DUSP9 has been studied.. This significantly limits the possibilities of using DUSP9 for clinical purposes. The purpose of this work was to find out whether it would be possible to detect DUSP9 in human urine. In the study we used human kidney carcinoma ACHN cells transfected with a vector, expressing DUSP9 and urine samples from 3 healthy volunteers. DUSP9 protein was detected by the Western blot method in precipitates obtained by centrifugation. We have shown that the DUSP9 protein is present in the pellet of the urine fraction obtained by low-speed centrifugation (10000 g). It is also present in the fraction of extracellular vesicles enriched with exosomes. The obtained result indicates that the analysis of DUSP9 expression is possible using a liquid biopsy, which, in turn, can significantly expand the applicability of this analysis for clinical purposes.

Biomedical Chemistry Research and MethodsVol. 8(1)
Russian Scientific Center of Radiology and Surgical Technologies (RU)
Openalex Percentile: Top 95%
Extracellular vesicles in disease
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.