Evidence map›Paper›PMID 41870841›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2026

Proteomic profiling of CD133 + and CD326 + (EpCAM) subpopulations in A549 cells: insights into pluripotency and tumor heterogeneity.

Fatih Ömerli, Medine Doğan Sarıkaya, Mustafa Burak Acar, Servet Özcan, Murat Çokkeçeci, Seçil Yılmaz

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In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Fatih ÖmerliGenome and Stem Cell Center (GENKOK), Erciyes University, Kayseri, Türkiye.
Medine Doğan SarıkayaGenome and Stem Cell Center (GENKOK), Erciyes University, Kayseri, Türkiye.
Mustafa Burak AcarGenome and Stem Cell Center (GENKOK), Erciyes University, Kayseri, Türkiye.
Servet ÖzcanGenome and Stem Cell Center (GENKOK), Erciyes University, Kayseri, Türkiye.
Murat ÇokkeçeciGenome and Stem Cell Center (GENKOK), Erciyes University, Kayseri, Türkiye.
Seçil YılmazGenome and Stem Cell Center (GENKOK), Erciyes University, Kayseri, Türkiye. siyilmaz@erciyes.edu.tr.ORCID http://orcid.org/0000-0001-9381-828X

Funding

Bilimsel Araştırma Projeleri, Erciyes Üniversitesi 12454
6 · The paper itself

Abstract

objectiveThis study aimed to isolate different cancer cell populations and characterize their secretome profiles to better understand their functional roles in metastasis and tumor progression. For this purpose, we analyzed the secretomes of CD133 and CD326 (EpCAM) positive subpopulations derived from the A549 cell line.

methodsCD133 positive (cancer stem cell marker) and CD326 positive (pluripotent stem cell marker) cells were isolated from the A549 non-small cell lung cancer cell line using magnetic cell separation. Secretome proteins from these subpopulations, along with parental A549 cells, were analyzed using bottom-up proteomics via liquid chromatography-tandem mass spectrometry (LC-MS/MS). The resulting datasets were further evaluated through bioinformatics analyses.

resultsCD133 positive cells were associated with angiogenesis, mesenchymal stem cell differentiation, and enhanced cell migration. In contrast, CD326 positive cells demonstrated pluripotent characteristics linked to epithelial-mesenchymal transition, neuronal differentiation, and placental morphogenesis, indicating a potential role in metastatic processes. Additionally, SERPINE2 and ADAM10 were identified as potential biomarkers for lung cancer, while YWHAZ and TRIM28 were associated with pluripotent cancer stem cell phenotypes.

conclusionThese findings support the existence of distinct cancer stem cell subtypes exhibiting multipotent and pluripotent properties. Secretome profiling provides valuable insights into tumor heterogeneity and highlights novel biomarker candidates, offering potential avenues for improved diagnosis and targeted therapeutic strategies in lung cancer.

Indexed as

AC133 AntigenCarcinoma, Non-Small-Cell LungEpithelial Cell Adhesion MoleculeLung NeoplasmsNeoplastic Stem CellsPluripotent Stem CellsA549 CellsBiomarkers, TumorCell DifferentiationEpithelial-Mesenchymal TransitionHumansProteomicsAC133 AntigenBiomarkers, TumorEPCAM protein, humanEpithelial Cell Adhesion MoleculePROM1 protein, humanCancer stem cellNon-small cell lung carcinomaProteomicsSecretome

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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.