ArticleInternational journal of clinical and experimental pathology2017
Prevalence of programmed death-1 ligand-1 (PD-L1) and infiltrating lymphocytes in human gastric carcinogenesis.
Article in International journal of clinical and experimental pathology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed, 3 citations in OpenAlex.
- Gastric organoids: A promising model for studying "inflammation-cancer" transition in atrophic gastritis.World journal of clinical oncology · 2025Review
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveThe PD-1/PD-L1 pathway plays a key role in the immune evasion of tumor cells from the host immune system. This study aimed to examine PD-L1 expression and prevalence of infiltrating T cellin gastric diseases, and elucidate the relevance of PD-L1 and prevalence of infiltrating T cell in the pathogenesis of gastric carcinoma.
methodsImmunohistochemistry and HE staining were used to investigate the
resultsThe expression of PD-L1 was found to be most prevalent in gastric carcinoma and, by comparison, decreased in gastric tissues from patients with gastric ulcer or intestinal metaplasia/atrophic gastritis. The overexpression of PD-L1 was notably more prevalent in cancer tissues and tissues from cases of intestinal metaplasia/atrophic gastritis, with the highest prevalence observed in intestinal metaplasia/atrophic gastritis. Meanwhile, decreasing prevalence was observed for CD4 and CD8 expression in gastric carcinoma. Therefore, PD-L1 expression in gastric carcinoma appeared to be inversely correlated with prevalence of infiltrating T cell.
conclusionPD-L1 expression was more prevalent while CD4 and CD8 expression were decreased in gastric carcinoma compared with gastric ulcer and intestinal metaplasia/atrophic gastritis. As the activated immunological status in gastric ulcerappears to switch to one of immunological suppression in intestinal metaplasia/atrophic gastritis and gastric carcinoma, this may suggest that the immune evasion associated with the PD-L1 pathway may be triggered in the pathogenesis of human gastric carcinoma.
Indexed as
Identifiers
31966537PMC6966033W3027215283What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.