| Literature DB >> 33862415 |
Koichi Sato1, Takeshi Uehara2, Tomoyuki Nakajima3, Mai Iwaya3, Yusuke Miyagawa4, Takayuki Watanabe5, Hiroyoshi Ota6.
Abstract
We investigated the expression of LGR5, the most robust and reliable known cancer stem cell (CSC) marker of colorectal cancer, and PD-L1 in tumor budding (TB), as well as clinicopathological features. Tissue microarrays (TMAs) were generated from TB samples from 32 stage II/III colorectal adenocarcinoma patients, and LGR5 expression in TMAs was evaluated by RNAscope, an extremely sensitive RNA in situ hybridization technique. LGR5 expression was significantly lower in the PD-L1-positive group than in the PD-L1-negative group (P = 0.0256). In the PD-L1-positive group, the tumor-infiltrating lymphocytes (TILs) score tended to be higher while the TNM stage was lower compared with the PD-L1 negative group (P = 0.0822 and P = 0.0765, respectively). There was no significant difference in Overall Survival between the PD-L1-positive and PD-L1-negative groups (log-rank test, P = 0.8218). This study showed that PD-L1-positive patients are a unique population with low LGR5 expression, and that LGR5-positive cells may be a promising therapeutic target in PD-L1-negative patients.Entities:
Keywords: Colorectal adenocarcinoma; Leucine-rich repeat-containing G-protein-coupled receptor 5; PD-L1; RNA in situ hybridization; Tumor budding
Year: 2021 PMID: 33862415 DOI: 10.1016/j.anndiagpath.2021.151739
Source DB: PubMed Journal: Ann Diagn Pathol ISSN: 1092-9134 Impact factor: 2.090