Evidence map›Paper›PMID 29560830›Full record

ArticleBMC systems biology2018

QSurface: fast identification of surface expression markers in cancers.

Yourae Hong, Choa Park, Nayoung Kim, Juyeon Cho, Sung Ung Moon, Jongmin Kim, Euna Jeong, Sukjoon Yoon

Open access · diamondAbstract read
In one paragraph

Article in BMC systems biology, 2018. 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
0.5field-weighted citation impact, top 32% 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, 11 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

8 authors at 1 institution in 1 country.

Yourae Hong
Choa Park
Nayoung KimDepartment of Biological Sciences, Sookmyung Women's University, Seoul, 140-742, Republic of Korea.
Juyeon ChoDepartment of Biological Sciences, Sookmyung Women's University, Seoul, 140-742, Republic of Korea.
Sung Ung MoonCenter for Advanced Bioinformatics & Systems medicine, Department of Biological Sciences, Sookmyung Women's University, Hyochangwon-gil 52, Yongsan-gu, Seoul, 140-742, Republic of Korea.
Jongmin KimDepartment of Biological Sciences, Sookmyung Women's University, Seoul, 140-742, Republic of Korea.
Euna JeongCenter for Advanced Bioinformatics & Systems medicine, Department of Biological Sciences, Sookmyung Women's University, Hyochangwon-gil 52, Yongsan-gu, Seoul, 140-742, Republic of Korea. eajeong@sookmyung.ac.kr.
Sukjoon YoonCenter for Advanced Bioinformatics & Systems medicine, Department of Biological Sciences, Sookmyung Women's University, Hyochangwon-gil 52, Yongsan-gu, Seoul, 140-742, Republic of Korea. yoonsj@sookmyung.ac.kr.
Sookmyung Women's University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCell surface proteins have provided useful targets and biomarkers for advanced cancer therapies. The recent clinical success of antibody-drug conjugates (ADCs) highlights the importance of finding selective surface antigens for given cancer subtypes. We thus attempted to develop stand-alone software for the analysis of the cell surface transcriptome of patient cancer samples and to prioritize lineage- and/or mutation-specific over-expression markers in cancer cells.

resultsA total of 519 genes were selected as surface proteins, and their expression was profiled in 14 cancer subtypes using patient sample transcriptome data. Lineage/mutation-oriented analysis was used to identify subtype-specific surface markers with statistical confidence. Experimental validation confirmed the unique over-expression of predicted surface markers (MUC4, MSLN, and SLC7A11) in lung cancer cells at the protein level. The differential cell surface gene expression of cell lines may differ from that of tissue samples due to the absence of the tumor microenvironment.

conclusionsIn the present study, advanced 3D models of lung cell lines successfully reproduced the predicted patterns, demonstrating the physiological relevance of cell line-based 3D models in validating surface markers from patient tumor data. Also QSurface software is freely available at http://compbio.sookmyung.ac.kr/~qsurface .

Indexed as

Gene Expression Regulation, NeoplasticAntigens, NeoplasmBiomarkers, TumorCell Line, TumorComputational BiologyGene Expression ProfilingHumansMesothelinMutationNeoplasmsTime FactorsAntigens, NeoplasmBiomarkers, TumorMesothelinMSLN protein, humanAntibody-drug conjugatesCancer mutationsCancer transcriptomeSoftware development

Identifiers

PMID29560830
PMCPMC5861488
OpenAlexW2790969351

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LicenceCC BY
Read underepoch 390

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.