Evidence map›Paper›PMID 32736533›Full record

ArticleBMC cancer2020

Rare osteosarcoma cell subpopulation protein array and profiling using imaging mass cytometry and bioinformatics analysis.

Izhar S Batth, Qing Meng, Qi Wang, Keila E Torres, Jared Burks, Jing Wang, Richard Gorlick, Shulin Li

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2020. 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
0.8field-weighted citation impact, top 30% 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, 13 citations in OpenAlex.

  1. Review
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  3. Article
  4. Review
  5. Article
  6. Review
  7. Canine and murine models of osteosarcoma.Veterinary pathology · 2022
    Review
  8. Review
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  10. Article
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 2 institutions in 1 country.

Izhar S BatthDepartment of Pediatrics-Research, Division of Pediatrics, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Qing MengDepartment of Laboratory Medicine, Division of Pathology and Laboratory Medicine, Houston, USA.
Qi WangDepartment of Bioinformatics and Computational Biology, Division of Science, Houston, USA.
Keila E TorresDepartment of Surgical Oncology, Division of Surgery, Houston, USA.
Jared BurksDepartment of Leukemia, Division of Cancer Medicine, UT MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Jing WangDepartment of Bioinformatics and Computational Biology, Division of Science, Houston, USA. jingwang@mdanderson.org.
Richard GorlickDepartment of Pediatrics-Research, Division of Pediatrics, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA.
Shulin LiDepartment of Pediatrics-Research, Division of Pediatrics, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX, 77030, USA. sli4@mdanderson.org.ORCID http://orcid.org/0000-0001-5657-4183
The University of Texas MD Anderson Cancer Center · USAnesthesiology and Surgical Oncology Research Group · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Develop CTC capture technology for both mesenchymal and non-mesenchymal tumorsR01EB026291 · NIBIB · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LI, SHULIN · 2018 to 2021
$1.4M
NCI NIH HHS P30 CA016672NIBIB NIH HHS R01 EB026291The National Institutes of Health through M.D. Anderson's Cancer Center Support Grant CA016672
6 · The paper itself

Abstract

backgroundSingle rare cell characterization represents a new scientific front in personalized therapy. Imaging mass cytometry (IMC) may be able to address all these questions by combining the power of MS-CyTOF and microscopy.

methodsWe have investigated this IMC method using < 100 to up to 1000 cells from human sarcoma tumor cell lines by incorporating bioinformatics-based t-Distributed Stochastic Neighbor Embedding (t-SNE) analysis of highly multiplexed IMC imaging data. We tested this process on osteosarcoma cell lines TC71, OHS as well as osteosarcoma patient-derived xenograft (PDX) cell lines M31, M36, and M60. We also validated our analysis using sarcoma patient-derived CTCs.

resultsWe successfully identified heterogeneity within individual tumor cell lines, the same PDX cells, and the CTCs from the same patient by detecting multiple protein targets and protein localization. Overall, these data reveal that our t-SNE-based approach can not only identify rare cells within the same cell line or cell population, but also discriminate amongst varied groups to detect similarities and differences.

conclusionsThis method helps us make greater inroads towards generating patient-specific CTC fingerprinting that could provide an accurate tumor status from a minimally-invasive liquid biopsy.

Indexed as

ActinsBiopsy, Fine-NeedleBone NeoplasmsCell Line, TumorComputational BiologyDNA Copy Number VariationsDNA FingerprintingHumansImage CytometryLiquid BiopsyNeoplastic Cells, CirculatingOsteosarcomaProtein Array AnalysisVimentinActinsVimentinCell surface vimentin (CSV)Circulating tumor cells (CTCs)Copy number variations (CNV)Cytometry time-of-flight (CyTOF)Fine needle aspirates (FNA)Fluorescence associated cell-sorting (FACS)Imaging mass cytometry (IMC)Patient-derived xenograft (PDX)Smooth muscle actin (SMA)T-distributed stochastic neighbor embedding (t-SNE)

Identifiers

PMID32736533
PMCPMC7395380
OpenAlexW3046879958

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.