Evidence map›Paper›PMID 31760702›Full record

ArticleThoracic cancer2020

Prognostic impact of CD34 and SMA in cancer-associated fibroblasts in stage I-III NSCLC.

Arik Bernard Schulze, Lars Henning Schmidt, Birthe Heitkötter, Sebastian Huss, Michael Mohr, Alessandro Marra, Ludger Hillejan, Dennis Görlich, Peter J Barth, Jan Rehkämper and 1 more

Open access · goldAbstract read
In one paragraph

Article in Thoracic cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 29 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

11 authors at 5 institutions in 2 countries.

Arik Bernard SchulzeDepartment of Medicine A, Hematology, Oncology and Pulmonary Medicine, University Hospital Muenster, Muenster, Germany.ORCID 0000-0002-1644-3573
Lars Henning SchmidtDepartment of Medicine A, Hematology, Oncology and Pulmonary Medicine, University Hospital Muenster, Muenster, Germany.
Birthe HeitkötterGerhard Domagk Institute of Pathology, University Hospital Muenster, Muenster, Germany.
Sebastian HussGerhard Domagk Institute of Pathology, University Hospital Muenster, Muenster, Germany.
Michael MohrDepartment of Medicine A, Hematology, Oncology and Pulmonary Medicine, University Hospital Muenster, Muenster, Germany.
Alessandro MarraDepartment of Thoracic Surgery, Rems-Murr-Klinikum Winnenden, Winnenden, Germany.
Ludger HillejanDepartment of Thoracic Surgery, Niels-Stensen-Kliniken Ostercappeln, Ostercappeln, Germany.
Dennis GörlichInstitute of Biostatistics and Clinical Research, Westfaelische Wilhelms-University Muenster, Muenster, Germany.
Peter J BarthGerhard Domagk Institute of Pathology, University Hospital Muenster, Muenster, Germany.
Jan RehkämperInstitute of Pathology, University of Cologne, Cologne, Germany.
Georg EversDepartment of Medicine A, Hematology, Oncology and Pulmonary Medicine, University Hospital Muenster, Muenster, Germany.
University Hospital Münster · DENetApp (United States) · USRems-Murr-Klinikum · DEUniversity of Cologne · DEUniversity of Münster · DE

Funding

Medizinische Fakultät, Westfälische Wilhelms-Universität Münster X_OA_1056_ProjektDEAL
6 · The paper itself

Abstract

backgroundEpithelial-to-mesenchymal transition (EMT) is a crucial step in lung cancer pathogenesis. Among others, cancer-associated fibroblasts (CAFs) are reported to regulate this process.

objectivesTo investigate the prognostic and clinical impact, we analyzed CD34+ and SMA+ CAFs in non-small cell lung cancer (NSCLC).

methodsRetrospectively, immunohistochemistry was performed to study stromal protein expression of both CD34 and SMA in 304 NSCLC patients with pTNM stage I-III disease. All tissue samples were embedded on tissue microarrays (TMAs).

resultsOur analysis revealed an association for CD34+ CAFs with G1/2 tumors and adenocarcinoma histology. Moreover CD34+ CAFs were identified as an independent prognostic factor (both for progression free survival [PFS] and overall survival [OS] in stage I-III NSCLC). Besides, SMA+ expression correlated with higher pTNM-tumor stages and lymphatic spread (pN stage). In turn, SMA-negativity was associated with improved PFS, but no prognostic impact was found on OS. Of interest, neither CD34+ CAFs nor SMA+ CAFs were associated with the primary tumor size, localization and depth of infiltration (pT stage).

conclusionsCD34 was identified as an independent prognostic marker in pTNM stage I-III NSCLC. Moreover, loss of CD34+ CAFs might influence the dedifferentiation of the NSCLC tumor from its cell origin. Finally, SMA+ CAFs are more prevalent in NSCLC tumors of higher stages and lymphonodal positive NSCLC. KEY POINTS: Expression of CD34 on cancer associated fibroblasts (CAFs) is an independent prognostic factor in stage I-III NSCLC. SMA+ cancer associated fibroblasts are associated with higher tumor stages in NSCLC and might contribute to tumor progression in NSCLC.

Indexed as

ActinsAgedAntigens, CD34Biomarkers, TumorCancer-Associated FibroblastsCarcinoma, Non-Small-Cell LungCombined Modality TherapyFemaleFollow-Up StudiesHumansLung NeoplasmsMaleMiddle AgedNeoplasm StagingRetrospective StudiesSurvival RateACTA2 protein, humanActinsAntigens, CD34Biomarkers, TumorCancer associated fibroblastCD34EMTNSCLCSMA

Identifiers

PMID31760702
PMCPMC6938745
OpenAlexW2990025971

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.