Evidence map›Paper›PMID 36453157›Full record

ArticleJournal of diabetes investigation2023

Diabetes mellitus impacts on expression of DNA mismatch repair protein PMS2 and tumor microenvironment in pancreatic ductal adenocarcinoma.

Xuekai Pan, Hiroki Mizukami, Yutaro Hara, Takahiro Yamada, Keisuke Yamazaki, Kazuhiro Kudoh, Yuki Takeuchi, Takanori Sasaki, Hanae Kushibiki, Akiko Igawa and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 33% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Xuekai PanDepartment of Pathology and Molecular Medicine, Hirosaki University Graduate School of Medicine, Aomori, Japan.
Hiroki MizukamiDepartment of Pathology and Molecular Medicine, Hirosaki University Graduate School of Medicine, Aomori, Japan.ORCID https://orcid.org/0000-0003-2920-582X
Yutaro HaraDepartment of Pathology and Molecular Medicine, Hirosaki University Graduate School of Medicine, Aomori, Japan.
Takahiro YamadaDepartment of Pathology and Molecular Medicine, Hirosaki University Graduate School of Medicine, Aomori, Japan.
Keisuke YamazakiDepartment of Pathology and Molecular Medicine, Hirosaki University Graduate School of Medicine, Aomori, Japan.
Kazuhiro KudohDepartment of Pathology and Molecular Medicine, Hirosaki University Graduate School of Medicine, Aomori, Japan.
Yuki TakeuchiDepartment of Pathology and Molecular Medicine, Hirosaki University Graduate School of Medicine, Aomori, Japan.
Takanori SasakiDepartment of Pathology and Molecular Medicine, Hirosaki University Graduate School of Medicine, Aomori, Japan.
Hanae KushibikiDepartment of Pathology and Molecular Medicine, Hirosaki University Graduate School of Medicine, Aomori, Japan.
Akiko IgawaDepartment of Pathology and Molecular Medicine, Hirosaki University Graduate School of Medicine, Aomori, Japan.
Kenichi HakamadaDepartment of Gastroenterological Surgery, Hirosaki University Graduate School of Medicine, Aomori, Japan.
Hirosaki University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

AIMS/

introductionThe mismatch repair (MMR) protein recognizes DNA replication errors and plays an important role in tumorigenesis, including pancreatic ductal adenocarcinoma (PDAC). Although PMS2, a MMR protein, is degraded under oxidative stress, the effects of diabetes are still unclear. Herein, we focused on whether diabetes affected MMR protein expression in PDAC. MATERIALS AND

methodsTissues from 61 surgically resected PDAC subjects were clinicopathologically analyzed. Immunohistochemical analysis was performed for MMR protein expression, oxidative stress, and immune cell infiltration. The change of MMR protein expression was assessed in PDAC cell lines under stimulation with 25 mM glucose and 500 μM palmitic acid. Survival curves were analyzed by the Kaplan-Meier method with the log-rank test.

resultsDiabetes complicated with dyslipidemia significantly decreased the expression of PMS2 in PDAC tissues with an inverse correlation with the degree of oxidative stress. Palmitic acid combined with high glucose induced degradation of PMS2 protein, enhancing oxidative stress in vitro. CD8

conclusionsThe different phases of diabetes have a major impact on PDAC by altering PMS2 expression and the tumor immune microenvironment, which can be targeted by an immune checkpoint inhibitor.

Indexed as

Carcinoma, Pancreatic DuctalDiabetes Mellitus, Type 2Pancreatic NeoplasmsDNA Mismatch RepairHumansMismatch Repair Endonuclease PMS2Palmitic AcidPrognosisTumor MicroenvironmentMismatch Repair Endonuclease PMS2Palmitic AcidPMS2 protein, humanDiabetes mellitusPancreatic ductal adenocarcinomaPMS2

Identifiers

PMID36453157
PMCPMC9807152
OpenAlexW4310565835

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.