Aristolochic acid‐related renal cell carcinoma exhibits a distinct tumor‐immune microenvironment favoring response to immune checkpoint blockade

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Auteurs principaux: Po‐Hung Lin, Jason Yongsheng Chan, Peiyong Guan, Jing Han Hong, Abner Herbert Lim, Cedric Chuan‐Young Ng, Joe Poh Sheng Yeong, Jing Yi Lee, Wei Liu, Jeffrey Chun Tatt Lim, See‐Tong Pang, Bin Tean Teh
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author Po‐Hung Lin
Jason Yongsheng Chan
Peiyong Guan
Jing Han Hong
Abner Herbert Lim
Cedric Chuan‐Young Ng
Joe Poh Sheng Yeong
Jing Yi Lee
Wei Liu
Jeffrey Chun Tatt Lim
See‐Tong Pang
Bin Tean Teh
author_facet Po‐Hung Lin
Jason Yongsheng Chan
Peiyong Guan
Jing Han Hong
Abner Herbert Lim
Cedric Chuan‐Young Ng
Joe Poh Sheng Yeong
Jing Yi Lee
Wei Liu
Jeffrey Chun Tatt Lim
See‐Tong Pang
Bin Tean Teh
Po‐Hung Lin
Jason Yongsheng Chan
Peiyong Guan
Jing Han Hong
Abner Herbert Lim
Cedric Chuan‐Young Ng
Joe Poh Sheng Yeong
Jing Yi Lee
Wei Liu
Jeffrey Chun Tatt Lim
See‐Tong Pang
Bin Tean Teh
collection Wiley Open Access
contents Aristolochic acid‐related renal cell carcinoma exhibits a distinct tumor‐immune microenvironment favoring response to immune checkpoint blockade Po‐Hung Lin Jason Yongsheng Chan Peiyong Guan Jing Han Hong Abner Herbert Lim Cedric Chuan‐Young Ng Joe Poh Sheng Yeong Jing Yi Lee Wei Liu Jeffrey Chun Tatt Lim See‐Tong Pang Bin Tean Teh The Journal of Pathology Abstract Immune checkpoint blockade (ICB) is currently the standard of care for metastatic renal cell carcinoma (RCC), but treatment responses remain unpredictable. Aristolochic acid (AA), a prevalent supplement additive in Taiwan, has been associated with RCC and induces signature mutations, although its effect on the tumor‐immune microenvironment (TIME) is unclear. We aimed to investigate the immune profile of AA‐positive RCCs and explore its potential role as a susceptible candidate for ICB. Tissue samples from 22 patients with clear cell RCC (ccRCC) were collected for whole‐exome sequencing to determine the genetic features and AA mutational signature (the discovery cohort). The corresponding RNA was sent for NanoString PanCancer IO 360 gene expression analysis to explore the immunological features. The formalin‐fixed, parafilm‐embedded slides of ccRCCs were sent for multiplex immunohistochemistry/immunofluorescence stain using Vectra system to evaluate the TIME. Tissues from two patients with metastatic RCC demonstrating complete response to ICB were sent for studies to validate the findings (the index patients). The results showed that AA mutational signatures with high tumor mutational burden (TMB) were present in 31.81% of the tumors in the discovery cohort. Three distinct clusters were observed through NanoString analysis. Clusters 1 and 3 were composed mainly of AA‐positive RCCs. Cluster 3 RCCs exhibited higher tumor inflammation signature scores and higher immune cell type scores. Vectra analysis revealed a higher percentage of CD15+ and BATF3+ cells in cluster 1, whereas the percentage of CD8+ cells was potentially higher in cluster 3. Strong AA mutational signatures were found in the tumors of two index patients, and both were grouped to cluster 3. In conclusion, AA may induce higher TMB and alter the immune microenvironment in RCCs, which makes the tumors more susceptible to ICB. © 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland. 10.1002/path.6349 http://creativecommons.org/licenses/by-nc/4.0/
doi_str_mv 10.1002/path.6349
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institution Wiley Open Access
license_str_mv http://creativecommons.org/licenses/by-nc/4.0/
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publisher Wiley
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spellingShingle Aristolochic acid‐related renal cell carcinoma exhibits a distinct tumor‐immune microenvironment favoring response to immune checkpoint blockade
Po‐Hung Lin
Jason Yongsheng Chan
Peiyong Guan
Jing Han Hong
Abner Herbert Lim
Cedric Chuan‐Young Ng
Joe Poh Sheng Yeong
Jing Yi Lee
Wei Liu
Jeffrey Chun Tatt Lim
See‐Tong Pang
Bin Tean Teh
The Journal of Pathology
Aristolochic acid‐related renal cell carcinoma exhibits a distinct tumor‐immune microenvironment favoring response to immune checkpoint blockade Po‐Hung Lin Jason Yongsheng Chan Peiyong Guan Jing Han Hong Abner Herbert Lim Cedric Chuan‐Young Ng Joe Poh Sheng Yeong Jing Yi Lee Wei Liu Jeffrey Chun Tatt Lim See‐Tong Pang Bin Tean Teh The Journal of Pathology Abstract Immune checkpoint blockade (ICB) is currently the standard of care for metastatic renal cell carcinoma (RCC), but treatment responses remain unpredictable. Aristolochic acid (AA), a prevalent supplement additive in Taiwan, has been associated with RCC and induces signature mutations, although its effect on the tumor‐immune microenvironment (TIME) is unclear. We aimed to investigate the immune profile of AA‐positive RCCs and explore its potential role as a susceptible candidate for ICB. Tissue samples from 22 patients with clear cell RCC (ccRCC) were collected for whole‐exome sequencing to determine the genetic features and AA mutational signature (the discovery cohort). The corresponding RNA was sent for NanoString PanCancer IO 360 gene expression analysis to explore the immunological features. The formalin‐fixed, parafilm‐embedded slides of ccRCCs were sent for multiplex immunohistochemistry/immunofluorescence stain using Vectra system to evaluate the TIME. Tissues from two patients with metastatic RCC demonstrating complete response to ICB were sent for studies to validate the findings (the index patients). The results showed that AA mutational signatures with high tumor mutational burden (TMB) were present in 31.81% of the tumors in the discovery cohort. Three distinct clusters were observed through NanoString analysis. Clusters 1 and 3 were composed mainly of AA‐positive RCCs. Cluster 3 RCCs exhibited higher tumor inflammation signature scores and higher immune cell type scores. Vectra analysis revealed a higher percentage of CD15+ and BATF3+ cells in cluster 1, whereas the percentage of CD8+ cells was potentially higher in cluster 3. Strong AA mutational signatures were found in the tumors of two index patients, and both were grouped to cluster 3. In conclusion, AA may induce higher TMB and alter the immune microenvironment in RCCs, which makes the tumors more susceptible to ICB. © 2024 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland. 10.1002/path.6349 http://creativecommons.org/licenses/by-nc/4.0/
title Aristolochic acid‐related renal cell carcinoma exhibits a distinct tumor‐immune microenvironment favoring response to immune checkpoint blockade
topic The Journal of Pathology
url https://pathsocjournals.onlinelibrary.wiley.com/doi/10.1002/path.6349