Evidence map›Paper›PMID 28652021›Full record

ArticleCancer letters2017

Detection of circulating tumor cells from cryopreserved human sarcoma peripheral blood mononuclear cells.

Heming Li, Qing H Meng, Hyangsoon Noh, Izhar Singh Batth, Neeta Somaiah, Keila E Torres, Xueqing Xia, Ruoyu Wang, Shulin Li

Abstract readValidation Study
In one paragraph

Article in Cancer letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 39 citations in OpenAlex.

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  5. Isolation and Characterization of Circulating Tumor Cells.Methods in molecular biology (Clifton, N.J.) · 2025
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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

9 authors at 2 institutions in 2 countries.

Heming LiDepartment of Oncology, Affiliated Zhongshan Hospital of Dalian University, Dalian, China. Electronic address: Hli15@mdanderson.org.
Qing H MengDepartment of Laboratory Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, United States. Electronic address: QHMeng@mdanderson.org.
Hyangsoon NohDepartment of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States. Electronic address: HNoh@mdanderson.org.
Izhar Singh BatthDepartment of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States. Electronic address: ISBatth@mdanderson.org.
Neeta SomaiahDepartment of Sarcoma Medical Oncology, Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, United States. Electronic address: NSomaiah@mdanderson.org.
Keila E TorresDepartment of Surgical Oncology, Division of Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, United States. Electronic address: ketorres@mdanderson.org.
Xueqing XiaDepartment of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States. Electronic address: XXia1@mdanderson.org.
Ruoyu WangDepartment of Oncology, Affiliated Zhongshan Hospital of Dalian University, Dalian, China. Electronic address: wangruoyu1963@163.com.
Shulin LiDepartment of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States. Electronic address: sli4@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USAffiliated Zhongshan Hospital of Dalian University · CN

Funding

Gene-Product Auto-Targeting to Tumor VesselsR01CA120895 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LI, SHULIN · 2007 to 2025
$4.8M
Fgl-2 targeted therapy for reversing multi-modality immune suppressionR01CA203493 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI HEIMBERGER, AMY BETH, LI, SHULIN · 2016 to 2020
$1.8M
NCI NIH HHS R01 CA120895NCI NIH HHS R01 CA203493
6 · The paper itself

Abstract

Circulating tumor cells (CTCs) enter the vasculature or lymphatic system after shedding from the primary tumor. CTCs may serve as "seed" cells for tumor metastasis. The utility of CTCs in clinical applications for sarcoma is not fully investigated, partly owing to the necessity for fresh blood samples and the lack of a CTC-specific antibody. To overcome these drawbacks, we developed a technique for sarcoma CTCs capture and detection using cryopreserved peripheral blood mononuclear cells (PBMCs) and our proprietary cell-surface vimentin (CSV) antibody 84-1, which is specific to tumor cells. This technique was validated by sarcoma cell spiking assay, matched CTCs comparison between fresh and cryopreserved PBMCs, and independent tumor markers in multiple types of sarcoma patient blood samples. The reproducibility was maximized when cryopreserved PBMCs were prepared from fresh blood samples within 2 h of the blood draw. In summary, as far as we are aware, ours is the first report to capture and detect CTCs from cryopreserved PBMCs. Further validation in other types of tumor may help boost the feasibility and utility of CTC-based diagnosis in a centralized laboratory.

Indexed as

CryopreservationBiomarkers, TumorBone NeoplasmsCell Line, TumorFluorescent Antibody TechniqueHumansImmunomagnetic SeparationLeukocytes, MononuclearNeoplastic Cells, CirculatingOsteosarcomaPredictive Value of TestsPrognosisReproducibility of ResultsTime FactorsVimentinBiomarkers, TumorVimentinCell surface vimentinCirculating tumor cellsCryopreservationPeripheral blood mononuclear cellsSarcoma

Identifiers

PMID28652021
PMCPMC5546157
OpenAlexW2630669046

What OpenQuestion holds

Textmetadata
LicenceTDM
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.