Evidence map›Paper›PMID 37369459›Full record

ArticleIn vivo (Athens, Greece)

Impact of Pattern Recognition Receptors on the Prognosis of Chemotherapy-treated Rectal Cancer Patients.

Chia-Lin Chang, Kevin Chih-Yang Huang, Tsung-Wei Chen, William Tzu-Liang Chen, Tao-Wei Ke, Yih-Farng Liou, K S Clifford Chao, Shu-Fen Chiang

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). 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
0.2field-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, 1 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

8 authors at 5 institutions in 2 countries.

Chia-Lin ChangDepartment of Hematology and Oncology, Ministry of Health and Welfare Feng Yuan Hospital, Taichung, Taiwan, R.O.C.
Kevin Chih-Yang HuangDepartment of Biomedical Imaging and Radiological Science, China Medical University, Taichung, Taiwan, R.O.C.
Tsung-Wei ChenDepartment of Pathology, Asia University Hospital, Asia University, Taichung, Taiwan, R.O.C.
William Tzu-Liang ChenDepartment of Colorectal Surgery, Hsinchu China Medical University Hospital, Hsinchu, Taiwan, R.O.C.
Tao-Wei KeDepartment of Colorectal Surgery, China Medical University Hospital, China Medical University, Taichung, Taiwan, R.O.C.
Yih-Farng LiouDepartment of Internal Medicine, Feng Yuan Hospital, Ministry of Health and Welfare, Taichung, Taiwan, R.O.C.
K S Clifford Chao *Graduate Institute of Biomedical Science, China Medical University, Taichung, Taiwan, R.O.C.; d94032@mail.cmuh.org.tw.
Shu-Fen Chiang *Laboratory of Precision Medicine, Ministry of Health and Welfare Feng Yuan Hospital, Taichung, Taiwan, R.O.C. suvenchiang@gmail.com.
China Medical University · TWTaichung Hospital · TWAsia University · TWChina Medical University Hospital · TWMinistry of Health and Welfare · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimChemotherapeutic drugs or radiation can cause immunogenic cell death (ICD) and damage-associated molecular pattern (DAMP) release to activate pattern recognition receptor (PRR) in immune cells. Several PRRs bridge innate immunity and adaptive immunity and are implicated in the anticancer immune response. However, single nucleotide polymorphisms (SNPs) in PRRs are associated with chemotherapeutic drugs or radiation response in cancer treatment. PATIENTS AND

methodsWe enrolled 117 patients with rectal cancer who received surgery with or without postoperative chemotherapy and examined the SNPs in PRRs from formalin-fixed, paraffin embedded tissues. The genotypes of RAGE (G82S/rs2070600), P2RX7 (E496A/rs3751143), and FPR1 (E346A/rs867228) were determined and analyzed using the MassARRAY platform.

resultsWe integrated the status of PRR polymorphism into the PRR score and found that the PRR score was significantly associated with 10-year disease-free survival (DFS) (p=0.025) in patients with rectal cancer. Moreover, the PRR score was an independent risk factor for 10-year DFS (HR=4.400, 95%CI=1.607-12.212, p=0.004) and 10-year overall survival (OS) (HR=4.674, 95%CI=1.423-16.038, p=0.011) in patients with rectal cancer treated postoperatively with adjuvant chemotherapy.

conclusionThe PRR score is an independent prognostic factor for the survival outcome of patients with rectal cancer, especially those treated postoperatively with adjuvant chemotherapy. PRR score evaluation may be used as a biomarker in the clinic.

Indexed as

Rectal NeoplasmsChemotherapy, AdjuvantDisease-Free SurvivalHumansPolymorphism, Single NucleotidePrognosisReceptors, Pattern RecognitionRectumReceptors, Pattern RecognitionPattern recognition receptorpostoperative adjuvant chemotherapyrectal cancersingle nucleotide polymorphisms

Identifiers

PMID37369459
PMCPMC10347908
OpenAlexW4382344191

What OpenQuestion holds

Textmetadata
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.