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EphrinB2: Expression of a novel potential target in renal cell carcinoma
INTRODUCTION: Renal cell carcinoma (RCC) is primarily managed by surgery with the use of systemic targeted therapy in a metastatic setting. Newer targeted therapeutic options are evolving; Eph-ephrin is a potential new pathway. The therapeutic potential of targeting the EphB4-EphrinB2 pathway has be...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419785/ https://www.ncbi.nlm.nih.gov/pubmed/37575160 http://dx.doi.org/10.4103/iju.iju_92_23 |
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author | Gupta, Chhavi Sali, Akash Pramod Jackovich, Alexandra Ma, Binyun Sadeghi, Sarmad Quinn, David Gill, Parkash Gill, Inderbir |
author_facet | Gupta, Chhavi Sali, Akash Pramod Jackovich, Alexandra Ma, Binyun Sadeghi, Sarmad Quinn, David Gill, Parkash Gill, Inderbir |
author_sort | Gupta, Chhavi |
collection | PubMed |
description | INTRODUCTION: Renal cell carcinoma (RCC) is primarily managed by surgery with the use of systemic targeted therapy in a metastatic setting. Newer targeted therapeutic options are evolving; Eph-ephrin is a potential new pathway. The therapeutic potential of targeting the EphB4-EphrinB2 pathway has been demonstrated in many solid tumors; however, its expression in RCC has only been evaluated in a few studies with limited cases. We herein determine the immunohistochemical expression of EphrinB2 in RCC. METHODS: A tissue microarray comprising 110 cases of different histological subtypes of RCC and 10 normal kidney tissues were stained with monoclonal anti-EphrinB2 antibody (Abcam, AB201512). The tumor and endothelial cells expressing the EphrinB2 were examined and its expression was correlated with sex, histological subtypes, and tumor nodes metastasis (TNM) stage. RESULTS: Twenty cases of urothelial carcinoma and two unsatisfactory conventional clear cell RCC cases were excluded, and EphrinB2 expression was interpreted in the remaining 88 tumors. EphrinB2 was expressed in 42 out of 88 tumors (47.7%) and was negative in the normal renal parenchyma. There was a statistically significant difference in the expression of EphrinB2 in males (55%) and females (32%). However, no such difference of expression was noted for the histological subtypes and the stages. Half (51%) of Stage 1 (n = 30) and Stage 2 (n = 11) tumors showed EphrinB2 positivity. CONCLUSIONS: EphrinB2 is expressed in approximately half of RCC cases. EphrinB2 expression in the early stage cancer might indicate its induction as an early event. |
format | Online Article Text |
id | pubmed-10419785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-104197852023-08-12 EphrinB2: Expression of a novel potential target in renal cell carcinoma Gupta, Chhavi Sali, Akash Pramod Jackovich, Alexandra Ma, Binyun Sadeghi, Sarmad Quinn, David Gill, Parkash Gill, Inderbir Indian J Urol Original Article INTRODUCTION: Renal cell carcinoma (RCC) is primarily managed by surgery with the use of systemic targeted therapy in a metastatic setting. Newer targeted therapeutic options are evolving; Eph-ephrin is a potential new pathway. The therapeutic potential of targeting the EphB4-EphrinB2 pathway has been demonstrated in many solid tumors; however, its expression in RCC has only been evaluated in a few studies with limited cases. We herein determine the immunohistochemical expression of EphrinB2 in RCC. METHODS: A tissue microarray comprising 110 cases of different histological subtypes of RCC and 10 normal kidney tissues were stained with monoclonal anti-EphrinB2 antibody (Abcam, AB201512). The tumor and endothelial cells expressing the EphrinB2 were examined and its expression was correlated with sex, histological subtypes, and tumor nodes metastasis (TNM) stage. RESULTS: Twenty cases of urothelial carcinoma and two unsatisfactory conventional clear cell RCC cases were excluded, and EphrinB2 expression was interpreted in the remaining 88 tumors. EphrinB2 was expressed in 42 out of 88 tumors (47.7%) and was negative in the normal renal parenchyma. There was a statistically significant difference in the expression of EphrinB2 in males (55%) and females (32%). However, no such difference of expression was noted for the histological subtypes and the stages. Half (51%) of Stage 1 (n = 30) and Stage 2 (n = 11) tumors showed EphrinB2 positivity. CONCLUSIONS: EphrinB2 is expressed in approximately half of RCC cases. EphrinB2 expression in the early stage cancer might indicate its induction as an early event. Wolters Kluwer - Medknow 2023 2023-06-30 /pmc/articles/PMC10419785/ /pubmed/37575160 http://dx.doi.org/10.4103/iju.iju_92_23 Text en Copyright: © 2023 Indian Journal of Urology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Gupta, Chhavi Sali, Akash Pramod Jackovich, Alexandra Ma, Binyun Sadeghi, Sarmad Quinn, David Gill, Parkash Gill, Inderbir EphrinB2: Expression of a novel potential target in renal cell carcinoma |
title | EphrinB2: Expression of a novel potential target in renal cell carcinoma |
title_full | EphrinB2: Expression of a novel potential target in renal cell carcinoma |
title_fullStr | EphrinB2: Expression of a novel potential target in renal cell carcinoma |
title_full_unstemmed | EphrinB2: Expression of a novel potential target in renal cell carcinoma |
title_short | EphrinB2: Expression of a novel potential target in renal cell carcinoma |
title_sort | ephrinb2: expression of a novel potential target in renal cell carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419785/ https://www.ncbi.nlm.nih.gov/pubmed/37575160 http://dx.doi.org/10.4103/iju.iju_92_23 |
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