Evidence map›Paper›PMID 30549153›Full record

ArticleCancer science2019

Live single cell mass spectrometry reveals cancer-specific metabolic profiles of circulating tumor cells.

Yasmine Abouleila, Kaoru Onidani, Ahmed Ali, Hirokazu Shoji, Takayuki Kawai, Chwee Teck Lim, Vipin Kumar, Shinobu Okaya, Ken Kato, Eiso Hiyama and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
5.0field-weighted citation impact, top 3% 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

67 citing papers in PubMed, 117 citations in OpenAlex.

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  8. Lipids: Driving Forces in the Underlying Biology of Carcinogenesis.ACS pharmacology & translational science · 2025
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7 more citing papers are in PubMed but not listed here.

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

14 authors at 8 institutions in 5 countries.

Yasmine AbouleilaRIKEN Center for Biosystems Dynamics research (BDR), Osaka, Japan.
Kaoru OnidaniDepartment of Biomarkers for Early Detection of Cancer, National Cancer Center Research Institute, Tokyo, Japan.
Ahmed AliRIKEN Center for Biosystems Dynamics research (BDR), Osaka, Japan.
Hirokazu ShojiDepartment of Biomarkers for Early Detection of Cancer, National Cancer Center Research Institute, Tokyo, Japan.
Takayuki KawaiRIKEN Center for Biosystems Dynamics research (BDR), Osaka, Japan.
Chwee Teck LimDepartment of Biomedical Engineering, National University of Singapore, Singapore.
Vipin KumarRIKEN Center for Biosystems Dynamics research (BDR), Osaka, Japan.
Shinobu OkayaDepartment of Biomarkers for Early Detection of Cancer, National Cancer Center Research Institute, Tokyo, Japan.
Ken KatoGastrointestinal Medical Oncology Division, National Cancer Center Hospital, Tokyo, Japan.
Eiso HiyamaNatural Science for Basic Research and Development, Hiroshima University, Hiroshima, Japan.
Toshio YanagidaRIKEN Center for Biosystems Dynamics research (BDR), Osaka, Japan.
Tsutomu MasujimaRIKEN Center for Biosystems Dynamics research (BDR), Osaka, Japan.
Yoshihiro ShimizuRIKEN Center for Biosystems Dynamics research (BDR), Osaka, Japan.ORCID https://orcid.org/0000-0003-3499-1394
Kazufumi HondaDepartment of Biomarkers for Early Detection of Cancer, National Cancer Center Research Institute, Tokyo, Japan.
RIKEN Center for Biosystems Dynamics Research · JPHiroshima University · JPNational Cancer Center · USJapan Agency for Medical Research and Development · JPNational Cancer Research Institute · GBNational University of Singapore · SGTokyo Dental College · JPUbe Frontier University · JP

Funding

AMED 18cm0106403 h0003AMED 18gm0710010h0105Ministry of Education, Culture, Sports, Science and Technology of JapanRIKEN Junior Research Associate ProgramRIKEN Single Cell Research Project
6 · The paper itself

Abstract

Recently, there has been increased attention on the analysis of circulating tumor cells (CTCs), also known as liquid biopsy, owing to its potential benefits in cancer diagnosis and treatment. Circulating tumor cells are released from primary tumor lesions into the blood stream and eventually metastasize to distant body organs. However, a major hurdle with CTC analysis is their natural scarcity. Existing methods lack sensitivity, specificity, or reproducibility required in CTC characterization and detection. Here, we report untargeted molecular profiling of single CTCs obtained from gastric cancer and colorectal cancer patients, using live single cell mass spectrometry integrated with microfluidics-based cell enrichment techniques. Using this approach, we showed the difference in the metabolomic profile between CTCs originating from different cancer groups. Moreover, potential biomarkers were putatively annotated to be specific to each cancer type.

Indexed as

AgedAged, 80 and overBiomarkers, TumorCell CountColorectal NeoplasmsFemaleHumansMaleMass SpectrometryMetabolomeMicrofluidicsMiddle AgedNeoplastic Cells, CirculatingReproducibility of ResultsBiomarkers, Tumorcancer biomarkercirculating tumor cellsliquid biopsymass spectrometrysingle cell analysis

Identifiers

PMID30549153
PMCPMC6361580
OpenAlexW2904740297

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.