Evidence map›Paper›PMID 38982031›Full record

ArticleCell proliferation2024

Impact of CD151 overexpression on prognosis and therapy in non-small cell lung cancer patients lacking EGFR mutations.

Amanda Huee-Ping Wong, Min En Nga, Chin Yein Chin, Yee Kit Tai, Hung Chew Wong, Ross Soo, Omer An, Henry Yang, Ju Ee Seet, Yaw Chyn Lim and 2 more

Abstract read
In one paragraph

Article in Cell proliferation, 2024. 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
–field-weighted citation impact
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.

  1. Article
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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

12 authors.

Amanda Huee-Ping WongDepartment of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0002-7738-2663
Min En NgaDepartment of Pathology, National University Hospital, Singapore, Singapore.
Chin Yein ChinDepartment of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Yee Kit TaiDepartment of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Hung Chew WongDepartment of Biostatistics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Ross SooDepartment of Haematology-Oncology, National University Hospital, Singapore, Singapore.
Omer AnCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0002-5762-6253
Henry YangCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
Ju Ee SeetDepartment of Pathology, National University Hospital, Singapore, Singapore.
Yaw Chyn LimDepartment of Pathology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
John Kit Chung TamDepartment of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0002-6269-3653
Thai TranDepartment of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID https://orcid.org/0000-0002-8662-3676

Funding

National University Health Systems Bench-to-bedside grant NUHSRO/2014/078/STB/B2B FY14/15NUHS Cross Department Collaborative Grant R-176-000-135-733
6 · The paper itself

Abstract

This study investigates CD151, a protein linked to cancer progression, in non-small cell lung cancer (NSCLC) patients without epidermal growth factor receptor (EGFR) mutations. These patients often have limited treatment options. The study used retrospective analysis to examine 157 adenocarcinoma biopsy specimens and 199 patient cases from The Cancer Genome Atlas, correlating CD151 expression with patient survival. Cellular studies revealed that CD151 interacts with EGFR, influencing epidermal growth factor (EGF)-induced cell proliferation and the effectiveness of the EGFR inhibitor, erlotinib. A strong association was found between CD151 expression and EGFR mutation status. High CD151 expression in the absence of EGFR mutations is correlated with poorer survival outcomes. Biological assays showed that CD151 colocalizes and associates with EGFR, playing a crucial role in regulating EGF-induced cell proliferation via the AKT and ERK1/2 pathways. Importantly, CD151 expression was found to influence the anti-proliferative effects of the EGFR tyrosine kinase inhibitor, erlotinib. High CD151 expression, in the absence of EGFR mutations, was associated with poorer survival outcomes. It could serve as a potential prognostic marker and influence cellular responses to EGFR-targeted treatments. This study highlights CD151 as a potential novel target for therapeutic intervention in NSCLC, especially in populations lacking EGFR mutations.

Indexed as

Carcinoma, Non-Small-Cell LungCell ProliferationErbB ReceptorsErlotinib HydrochlorideLung NeoplasmsMutationTetraspanin 24AgedCell Line, TumorFemaleHumansMaleMiddle AgedPrognosisProtein Kinase InhibitorsRetrospective StudiesCD151 protein, humanEGFR protein, humanErbB ReceptorsErlotinib HydrochlorideProtein Kinase InhibitorsTetraspanin 24

Identifiers

PMID38982031
PMCPMC11503249

What OpenQuestion holds

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LicenceCC BY
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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.