Evidence map›Paper›PMID 36309388›Full record

ArticleIn vivo (Athens, Greece)

Fc Receptor Expression as a Prognostic Factor in Patients With Non-small-cell Lung Cancer.

Min Hye Kim, Jeong Hee Lee, Jong Sil Lee, Dong Chul Kim, Jung Wook Yang, Hyo Jung An, Ji Min Na, Meong Cheol Shin, Dae Hyun Song

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Min Hye KimDepartment of Pathology, Gyeongsang National University Hospital, Jinju, Republic of Korea.
Jeong Hee LeeDepartment of Pathology, Gyeongsang National University Hospital, Jinju, Republic of Korea.
Jong Sil LeeDepartment of Pathology, Gyeongsang National University Hospital, Jinju, Republic of Korea.
Dong Chul KimDepartment of Pathology, Gyeongsang National University Hospital, Jinju, Republic of Korea.
Jung Wook YangDepartment of Pathology, Gyeongsang National University Hospital, Jinju, Republic of Korea.
Hyo Jung AnDepartment of Pathology, Gyeongsang National University School of Medicine, Jinju, Republic of Korea.
Ji Min NaDepartment of Pathology, Gyeongsang National University Hospital, Jinju, Republic of Korea.
Meong Cheol ShinResearch Institute of Pharmaceutical Sciences, College of Pharmacy, Gyeongsang National University, Jinju, Republic of Korea.
Dae Hyun SongDepartment of Pathology, Gyeongsang National University School of Medicine, Jinju, Republic of Korea; golgy@hanmail.net.
Gyeongsang National University · KRGyeongsang National University Hospital · KRChangwon National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimThe neonatal Fc receptor (FcRn) is a major histocompatibility class I-like molecule responsible for the transfer of passive humoral immunity from a mother to her newborn. Recent research revealed that FcRn is involved in antigen-presentation, humoral immunity and antitumor immunity of various types of cancer, such as lung, colon and breast. Lung cancer is the leading cause of cancer-related death and non-small cell lung cancer (NSCLC) accounts for 85% of all lung cancer. NSCLC is a highly heterogeneous disease and this affects the prognosis. Therefore, many studies have tried to identify factors that are associated with prognosis. The lungs are a major organ expressing FcRn. We aimed to evaluate FcRn expression in surgical specimens of NSCLC and determine its correlation with patient prognosis. MATERIALS AND

methodsWe analyzed 140 NSCLC surgical specimens for FcRn expression using immunohistochemistry and correlated positivity with clinicopathology and survival of these patients. A chi-squared test and Kaplan-Meier analysis with log-rank tests were performed for statistical evaluation.

resultsThe FcRn-positive group had a significantly higher disease-free survival and a tendency towards increased disease-specific survival in patients with tumor-node-metastasis stage I NSCLC.

conclusionOur study supports the hypothesis that FcRn down-regulation is associated with NSCLC progression.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsBiomarkers, TumorFemaleHumansInfant, NewbornKaplan-Meier EstimatePrognosisReceptors, FcBiomarkers, TumorReceptors, FcFc receptorlung cancer prognosisnon-small-cell lung cancerprognosissurvival analysis

Identifiers

PMID36309388
PMCPMC9677804
OpenAlexW4307844550

What OpenQuestion holds

Textmetadata
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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.