TY - JOUR
T1 - Renin Production by Juxtaglomerular Cell Tumors and Clear Cell Renal Cell Carcinoma and the Role of Angiotensin Signaling Inhibitors
AU - Gupta, Sounak
AU - Nichols, Paige
AU - Lohse, Christine M.
AU - Kosari, Farhad
AU - Kattah, Andrea G.
AU - Harris, Faye R.
AU - Karagouga, Giannoula
AU - Mehra, Rohit
AU - Fine, Samson W.
AU - Reuter, Victor E.
AU - Herrera-Hernandez, Loren
AU - Zganjar, Andrew J.
AU - Britton, Cameron J.
AU - Potretzke, Aaron M.
AU - Boorjian, Stephen A.
AU - Thompson, R. Houston
AU - Jimenez, Rafael E.
AU - Leibovich, Bradley C.
AU - Garovic, Vesna D.
AU - Cheville, John C.
AU - Sharma, Vidit
N1 - Funding Information:
The authors would like to thank Katelyn A. Reed for administrative assistance; LouAnn Gross for assistance with optimization of renin immunohistochemistry; and Dr Patricia T. Greipp, Ryan Knudson, and Sara Kloft-Nelson in the Mayo Clinic cytogenetics core facility for assistance with fluorescence in situ hybridization. Drs Gupta and Nichols contributed equally to this work.
Publisher Copyright:
© 2022 Mayo Foundation for Medical Education and Research
PY - 2022/11
Y1 - 2022/11
N2 - Objective: To profile juxtaglomerular cell tumors (JXG) and histologic mimics by analyzing renin expression; to identify non-JXG renin-producing tumors in The Cancer Genome Atlas (TCGA) data sets; and to define the prevalence of hypertension (HTN) and patient outcomes with angiotensin signaling inhibitor (ASI) use in tumors of interest. Patients and Methods: Thirteen JXGs and 10 glomus tumors (GTs), a histologic mimic, were evaluated for clinicopathologic features; TCGA data were analyzed to identify non-JXG renin-overexpressing tumors. An institutional registry was queried to determine the incidence of HTN, the use of ASIs in hypertensive patients, and the impact of ASIs on outcomes including progression-free survival (PFS) in a tumor type with high renin expression (clear cell renal cell carcinoma [CC-RCC] diagnosed between January 1, 2005, and December 31, 2012). Results: We found an association between renin production and HTN in JXG compared with GT. Analysis of TCGA data found that a subset of CC-RCCs overexpress renin relative to 29 other tumor types. Furthermore, analysis of our institutional registry revealed a high prevalence (64%) of HTN among 1203 patients treated with radical or partial nephrectomy for nonmetastatic CC-RCC. On multivariable Cox regression, patients with HTN treated with ASIs (34%) had improved PFS (hazard ratio, 0.76; 95% CI, 0.57 to 1.00; P=.05) compared with patients with HTN not treated with ASIs (30%). Conclusion: The identification of renin expression in a subset of CC-RCC may provide a biologic rationale for the high prevalence of HTN and improved PFS with ASI use in hypertensive patients with nonmetastatic CC-RCC.
AB - Objective: To profile juxtaglomerular cell tumors (JXG) and histologic mimics by analyzing renin expression; to identify non-JXG renin-producing tumors in The Cancer Genome Atlas (TCGA) data sets; and to define the prevalence of hypertension (HTN) and patient outcomes with angiotensin signaling inhibitor (ASI) use in tumors of interest. Patients and Methods: Thirteen JXGs and 10 glomus tumors (GTs), a histologic mimic, were evaluated for clinicopathologic features; TCGA data were analyzed to identify non-JXG renin-overexpressing tumors. An institutional registry was queried to determine the incidence of HTN, the use of ASIs in hypertensive patients, and the impact of ASIs on outcomes including progression-free survival (PFS) in a tumor type with high renin expression (clear cell renal cell carcinoma [CC-RCC] diagnosed between January 1, 2005, and December 31, 2012). Results: We found an association between renin production and HTN in JXG compared with GT. Analysis of TCGA data found that a subset of CC-RCCs overexpress renin relative to 29 other tumor types. Furthermore, analysis of our institutional registry revealed a high prevalence (64%) of HTN among 1203 patients treated with radical or partial nephrectomy for nonmetastatic CC-RCC. On multivariable Cox regression, patients with HTN treated with ASIs (34%) had improved PFS (hazard ratio, 0.76; 95% CI, 0.57 to 1.00; P=.05) compared with patients with HTN not treated with ASIs (30%). Conclusion: The identification of renin expression in a subset of CC-RCC may provide a biologic rationale for the high prevalence of HTN and improved PFS with ASI use in hypertensive patients with nonmetastatic CC-RCC.
UR - http://www.scopus.com/inward/record.url?scp=85133290898&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85133290898&partnerID=8YFLogxK
U2 - 10.1016/j.mayocp.2022.03.034
DO - 10.1016/j.mayocp.2022.03.034
M3 - Article
C2 - 35753824
AN - SCOPUS:85133290898
SN - 0025-6196
VL - 97
SP - 2050
EP - 2064
JO - Mayo Clinic proceedings
JF - Mayo Clinic proceedings
IS - 11
ER -