Evidence map›Paper›PMID 30535430›Full record

ArticleInternational journal of oncology2019

Pathways regulating the expression of the immunomodulatory protein glycodelin in non‑small cell lung cancer.

Rebecca Weber, Michael Meister, Thomas Muley, Michael Thomas, Holger Sültmann, Arne Warth, Hauke Winter, Felix J F Herth, Marc A Schneider

Open access · bronzeAbstract read
In one paragraph

Article in International journal of oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

12 citing papers in PubMed, 19 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.

Rebecca WeberTranslational Research Unit, Thoraxklinik at Heidelberg University Hospital, 69126 Heidelberg, Germany.
Michael MeisterTranslational Research Unit, Thoraxklinik at Heidelberg University Hospital, 69126 Heidelberg, Germany.
Thomas MuleyTranslational Research Unit, Thoraxklinik at Heidelberg University Hospital, 69126 Heidelberg, Germany.
Michael ThomasTranslational Lung Research Center Heidelberg, member of the German Centre for Lung Research (DZL‑TLRC), 69120 Heidelberg, Germany.
Holger SültmannTranslational Lung Research Center Heidelberg, member of the German Centre for Lung Research (DZL‑TLRC), 69120 Heidelberg, Germany.
Arne WarthTranslational Lung Research Center Heidelberg, member of the German Centre for Lung Research (DZL‑TLRC), 69120 Heidelberg, Germany.
Hauke WinterTranslational Lung Research Center Heidelberg, member of the German Centre for Lung Research (DZL‑TLRC), 69120 Heidelberg, Germany.
Felix J F HerthTranslational Lung Research Center Heidelberg, member of the German Centre for Lung Research (DZL‑TLRC), 69120 Heidelberg, Germany.
Marc A SchneiderTranslational Research Unit, Thoraxklinik at Heidelberg University Hospital, 69126 Heidelberg, Germany.
German Center for Lung Research · DEUniversity Hospital Heidelberg · DEHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glycodelin [gene name, progesterone associated endometrial protein (PAEP)] was initially described as an immune system modulator in reproduction. Today, it is also known to be expressed in several types of cancer, including non‑small cell lung cancer (NSCLC). In this cancer type, the feasibility of its usage as a follow‑up biomarker and its potential role as an immune system modulator were described. It is assumed that NSCLC tumours secrete glycodelin to overcome immune surveillance. Therefore, targeting glycodelin might be a future approach with which to weaken the immune system defence of NSCLC tumours. In this context, it is important to understand the regulatory pathways of PAEP/glycodelin expression, as these are mostly unknown so far. In this study, we analysed the influence of several inducers and of their downstream pathways on PAEP/glycodelin expression in a human lung adenocarcinoma carcinoma (ADC; H1975) and a human lung squamous cell carcinoma (SQCC) cell line (2106T). PAEP/glycodelin expression was notably stimulated by the canonical transforming growth factor (TGF)‑β pathway in SQCC cells and the PKC signalling cascade in both cell lines. The PI3K/AKT pathway inhibited PAEP/glycodelin expression in the ADC cells and an antagonizing role towards the other investigated signalling cascades is suggested herein. Furthermore, the mitogen‑activated protein kinase kinase (MEK)/extracellular‑signal regulated kinases (ERK) pathway was, to a lesser extent, found to be associated with increased PAEP/glycodelin amounts. The phosphoinositide 3‑kinase (PI3K)/protein kinase B (AKT), MEK/ERK pathway and TGF‑β are targets of NSCLC drugs that are already approved or are currently under investigation. On the whole, the findings of this study provide evidence that inhibiting these targets affects the expression of glycodelin and its immunosuppressive effect in NSCLC tumours. Moreover, understanding the regulation of glycodelin expression may lead to the development of novel therapeutic approaches with which to weaken the immune system defence of NSCLC tumours in the future.

Indexed as

Carcinoma, Non-Small-Cell LungCell Line, TumorCell ProliferationGene DeletionGene Expression Regulation, NeoplasticGlycodelinHumansImmunologic FactorsPhosphatidylinositol 3-KinasesProtein Kinase CProto-Oncogene Proteins c-aktRNA, Small InterferingSignal TransductionTransforming Growth Factor betaGlycodelinImmunologic FactorsPhosphatidylinositol 3-KinasesProtein Kinase CProto-Oncogene Proteins c-aktRNA, Small InterferingTransforming Growth Factor betaglycodelinimmunomodulatorynon-small cell lung cancerprogesterone associated endometrial proteinprotein kinase Bprotein kinase Csignalling pathwaystransforming growth factor-β

Identifiers

PMID30535430
PMCPMC6317686
OpenAlexW2902133413

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.