Evidence map›Paper›PMID 26632716›Full record

Observational studyMedicine2015

Expression of LRIG1 is Associated With Good Prognosis for Human Non-small Cell Lung Cancer.

Yuzhi An, Zibo Zhao, Pengju Ou, Guangchuan Wang

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. The European respiratory journal · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Lrig1 Expression in Human Sebaceous Gland Tumors.Dermatopathology (Basel, Switzerland)
    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

4 authors at 3 institutions in 2 countries.

Yuzhi AnFrom the Department of Oncology, the First Affiliated Hospital of Liaoning Medical University, Jinzhou, Liaoning, P.R. China (YA); Department of Oncology, University of Wisconsin-Madison, Madison, WI (ZZ); and Department of Immunology, Liaoning Medical University, Jinzhou, Liaoning, P.R. China (PO, GW).
Zibo Zhao
Pengju Ou
Guangchuan Wang
First Affiliated Hospital of Liaoning Medical University · CNJinzhou Medical University · CNUniversity of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Somatic mutations, which are associated with a certain rate of response to targeted therapies, are ubiquitously found in human non-small cell lung cancer (NSCLC). However, it is largely unknown which group of patients may benefit from the respective treatments targeting different somatic mutations. Therefore, more effective prognostic and predictive markers are desperately needed for the treatment of NSCLC harboring different somatic mutations. The leucine-rich repeats and immunoglobulin-like domains (LRIG)-1 is a tumor suppressor gene that belongs to the LRIG family. LRIG1 expression has prognostic significance in various human cancers.In this study, we first used the quantitative polymerase chain reaction (qPCR) and immunohistochemical analysis of 36 and 182 NSCLC patient tissues to analyze the LRIG1 expression respectively. To investigate the prognostic value of LRIG1 in NSCLC, we examined the correlation between clinical features and overall survival (OS) with Cox proportional hazard regression. We also compared the sensitivity and specificity of LRIG1 in NSCLC prognosis by logistic regression to further evaluate the prognostic efficiency of LRIG1 in NSCLC.We found that the LRIG1 expression was associated with pathological type, differentiation status, and stage of NSCLC. The result showed that LRIG1 was an independent prognostic factor for OS of NSCLC patients. LRIG1 in combination with other clinicopathological risk factors was a stronger prognostic model than clinicopathological risk factors alone.Thus, the LRIG1 expression potentially offered a significant clinical value in directing personal treatment for NSCLC patients.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsChinaFemaleGene Expression ProfilingHumansImmunohistochemistryMaleMembrane GlycoproteinsMiddle AgedNeoplasm StagingPredictive Value of TestsPrognosisProportional Hazards ModelsLRIG1 protein, humanMembrane Glycoproteins

Identifiers

PMID26632716
PMCPMC5058985
OpenAlexW2334858923

What OpenQuestion holds

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Registered trials

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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.