The effects of ARID1A mutations on colorectal cancer and associations with PD‐L1 expression by stromal cells. Issue 1 (27th May 2021)

• Record Type: Journal Article
• Authors: Kamori, Tomohiro; Oki, Eiji; Shimada, Yoshifumi; Hu, Qingjiang; Hisamatsu, Yuichi; Ando, Koji; Shimokawa, Mototsugu; Wakai, Toshifumi; Oda, Yoshinao; Mori, Masaki
• Is Part Of: Cancer reports. Volume 5:Issue 1(2022)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2021-05-27
• Subjects: ARID1A -- colorectal cancer -- microsatellite instability -- PD‐L1; Cancer -- Periodicals; 616.994005
• DOI: 10.1002/cnr2.1420
• Languages: English
• ISSNs: 2573-8348

Abstract

Abstract: Background: ARID1A is a component of the SWI/SNF complex, which controls the accessibility of proteins to DNA. ARID1A mutations are frequently observed in colorectal cancers (CRCs) and have been reported to be associated with high mutational burden and tumor PD‐L1 expression in vitro. Aim: To clarify the role of ARID1A mutation in CRC. Method and results: We used next generation sequencing (NGS) and immunohistochemistry on clinically obtained samples. A total of 201 CRC tissues from Niigata University and Niigata Center Hospital were processed by NGS using the CANCERPLEX panel. Immunohistochemistry for ARID1A, PD‐L1, MLH1, and MSH2 was performed on 66 propensity‐matched (33 microsatellite instability‐high [MSI‐H] and 33 microsatellite‐stable [MSS]) cases among 499 cases from Kyushu University. TCGA data were downloaded from cBioPortal. NGS showed significantly more mutations in ARID1A mutated CRCs ( p = 0.01), and the trend was stronger for right‐sided CRCs than left‐sided. TCGA data confirmed these findings ( p < 0.01). BRAF V600E and ATM mutations were also found at higher frequencies. Immunohistochemistry showed that 30% of MSI‐H CRCs had ARID1A loss, while this was true in only 6% of MSS CRCs. In both MSI‐H and MSS, PD‐L1 expression by stromal cells was enhanced in the ARID1A ‐mutant groups (90% vs 39% in MSI‐H, 100% vs 26% in MSS). Conclusion: We found a higher mutational burden in ARID1A ‐mutant CRCs, and IHC study showed that ARID1A loss was correlated with high PD‐L1 expression in stromal cells regardless of MSI status. These data support the idea that mutant ARID1A is a potential biomarker for CRCs.