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Abstract

Renal cell carcinoma (RCC) ranks among the most prevalent malignancies in Western countries, marked by its notable heterogeneity, which contributes to an unpredictable clinical trajectory. The insufficiency of dependable biomarkers adds complexity to assessing this tumor progression. Imbalances of several components of the intrarenal renin–angiotensin system (iRAS) significantly impact patient prognoses and responses to first-line immunotherapies. In this study, we analyzed the immunohistochemical expression of the Mas-related G-protein-coupled receptor D (MrgD), which recognizes the novel RAS peptide alamandine (ALA), in a series of 87 clear cell renal cell (CCRCCs), 19 papillary (PRCC), 7 chromophobe (ChRCC) renal cell carcinomas, and 11 renal oncocytomas (RO). MrgD was expressed in all the renal tumor subtypes, with a higher mean staining intensity in the PRCCs, ChRCCs, and ROs. A high expression of MrgD at the tumor center and at the infiltrative front of CCRCC tissues was significantly associated with a high histological grade, large tumor diameter, local invasion, and locoregional node and distant metastasis. Patients with worse 5-year cancer-specific survival and a poorer response to antiangiogenic tyrosine-kinase inhibitors (TKIs) showed higher MrgD expression at the center of their primary tumors. These findings suggest a possible role of MrgD in renal carcinogenetic processes. Further studies are necessary to unveil its potential as a novel biomarker for CCRCC prognosis and response to frontline therapies.

Details

1009240
Title
The Expression of Alamandine Receptor MrgD in Clear Cell Renal Cell Carcinoma Is Associated with a Worse Prognosis and Unfavorable Response to Antiangiogenic Therapy
Author
Larrinaga, Gorka 1 ; Valdivia, Asier 2   VIAFID ORCID Logo  ; Arrieta-Aguirre, Inés 3 ; Jon Danel Solano-Iturri 4 ; Ugalde-Olano, Aitziber 5 ; Loizaga-Iriarte, Ana 6 ; Santos-Martín, Aida 6 ; Pérez-Fernández, Amparo 6 ; Angulo, Javier C 7   VIAFID ORCID Logo  ; López, José I 8   VIAFID ORCID Logo 

 Department of Nursing, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain; [email protected]; Department of Physiology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain; Biobizkaia Health Research Institute, 48903 Barakaldo, Spain; [email protected] (J.D.S.-I.); [email protected] (A.U.-O.); [email protected] (A.L.-I.); [email protected] (A.S.-M.); [email protected] (A.P.-F.); [email protected] (J.I.L.) 
 Department of Cellular Biology and Histology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain; [email protected] 
 Department of Nursing, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain; [email protected] 
 Biobizkaia Health Research Institute, 48903 Barakaldo, Spain; [email protected] (J.D.S.-I.); [email protected] (A.U.-O.); [email protected] (A.L.-I.); [email protected] (A.S.-M.); [email protected] (A.P.-F.); [email protected] (J.I.L.); Department of Pathology, Cruces University Hospital, 48903 Barakaldo, Spain 
 Biobizkaia Health Research Institute, 48903 Barakaldo, Spain; [email protected] (J.D.S.-I.); [email protected] (A.U.-O.); [email protected] (A.L.-I.); [email protected] (A.S.-M.); [email protected] (A.P.-F.); [email protected] (J.I.L.); Department of Pathology, Basurto University Hospital, 48903 Barakaldo, Spain 
 Biobizkaia Health Research Institute, 48903 Barakaldo, Spain; [email protected] (J.D.S.-I.); [email protected] (A.U.-O.); [email protected] (A.L.-I.); [email protected] (A.S.-M.); [email protected] (A.P.-F.); [email protected] (J.I.L.); Department of Urology, Basurto University Hospital, University of the Basque Country (UPV/EHU), 48013 Bilbao, Spain 
 Clinical Department, Faculty of Medical Sciences, European University of Madrid, 28905 Getafe, Spain; [email protected]; Department of Urology, University Hospital of Getafe, 28907 Madrid, Spain 
 Biobizkaia Health Research Institute, 48903 Barakaldo, Spain; [email protected] (J.D.S.-I.); [email protected] (A.U.-O.); [email protected] (A.L.-I.); [email protected] (A.S.-M.); [email protected] (A.P.-F.); [email protected] (J.I.L.) 
Volume
25
Issue
3
First page
1499
Publication year
2024
Publication date
2024
Publisher
MDPI AG
Place of publication
Basel
Country of publication
Switzerland
ISSN
16616596
e-ISSN
14220067
Source type
Scholarly Journal
Language of publication
English
Document type
Journal Article
Publication history
 
 
Online publication date
2024-01-25
Milestone dates
2023-12-11 (Received); 2024-01-23 (Accepted)
Publication history
 
 
   First posting date
25 Jan 2024
ProQuest document ID
2923976415
Document URL
https://www.proquest.com/scholarly-journals/expression-alamandine-receptor-mrgd-clear-cell/docview/2923976415/se-2?accountid=208611
Copyright
© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Last updated
2024-08-27
Database
ProQuest One Academic