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The Genes—Candidates for Prognostic Markers of Metastasis by Expression Level in Clear Cell Renal Cell Cancer

Authors :
Alexander Karpukhin
Anna Markova
Maria V Peters
Natalya Apanovich
Vsevolod Matveev
Danzan Mansorunov
Pavel Apanovich
Source :
Diagnostics, Volume 10, Issue 1, Diagnostics, Vol 10, Iss 1, p 30 (2020)
Publication Year :
2020
Publisher :
Multidisciplinary Digital Publishing Institute, 2020.

Abstract

The molecular prognostic markers of metastasis are important for personalized approaches to clear cell renal cell carcinoma (ccRCC) treatment but markers for practical use are still missing. To address this gap we studied the expression of ten genes&mdash<br />CA9, NDUFA4L2, VWF, IGFBP3, BHLHE41, EGLN3, SAA1, CSF1R, C1QA, and FN1&mdash<br />through RT-PCR, in 56 ccRCC patients without metastases and with metastases. All of these, excluding CSF1R, showed differential and increased (besides SAA1) expression in non-metastasis tumors. The gene expression levels in metastasis tumors were decreased, besides CSF1R, FN1 (not changed), and SAA1 (increased). There were significant associations of the differentially expressed genes with ccRCC metastasis by ROC analysis and the Fisher exact test. The association of the NDUFA4L2, VWF, EGLN3, SAA1, and C1QA expression with ccRCC metastasis is shown for the first time. The CA9, NDUFA4L2, BHLHE4, and EGLN3 were distinguished as the strongest candidates for ccRCC metastasis biomarkers. We used an approach that presupposed that the metastasis marker was the expression levels of any three genes from the selected panel and received sensitivity (88%) and specificity (73%) levels with a relative risk of RR &gt<br />3. In conclusion, a panel of selected genes&mdash<br />the candidates in biomarkers of ccRCC metastasis&mdash<br />was created for the first time. The results might shed some light on the ccRCC metastasis processes.

Details

Language :
English
ISSN :
20754418
Database :
OpenAIRE
Journal :
Diagnostics
Accession number :
edsair.doi.dedup.....25ef3bb9c9fe7ac78c7aa0a5191277dc
Full Text :
https://doi.org/10.3390/diagnostics10010030