Evidence map›Paper›PMID 31767014›Full record

ArticleJournal of nanobiotechnology2019

High sensitive detection of circulating tumor cell by multimarker lipid magnetic nanoparticles and clinical verifications.

Jingde Chen, Lin Chen, Shibin Du, Jing Wu, Ming Quan, Hua Yin, Yin Wu, Xuanting Ye, Xiaofei Liang, Hong Jiang

Open access · goldAbstract read
In one paragraph

Article in Journal of nanobiotechnology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 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

10 authors at 3 institutions in 1 country.

Jingde ChenDepartment of Oncology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, 200120, China.
Lin ChenDepartment of Oncology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, 200120, China.
Shibin DuState Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200032, China.
Jing WuDepartment of Oncology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, 200120, China.
Ming QuanDepartment of Oncology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, 200120, China.
Hua YinDepartment of Gastrointestinal Surgery, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, 200120, China.
Yin WuDepartment of Oncology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, 200120, China.
Xuanting YeSeventh People's Hospital of Shanghai University of Traditional Chinese Medicine, 358 Datong Rd, Shanghai, 200137, People's Republic of China.
Xiaofei LiangState Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200032, China. xfliang86@126.com.
Hong JiangSeventh People's Hospital of Shanghai University of Traditional Chinese Medicine, 358 Datong Rd, Shanghai, 200137, People's Republic of China. jianghong2046@126.com.ORCID http://orcid.org/0000-0003-2550-8401
Shanghai East Hospital · CNRenji Hospital · CNShanghai University of Traditional Chinese Medicine · CN

Funding

Natural Science Foundation of Shanghai (CN) 201740038Shanghai Young Physician Training Program【2015】 147.
6 · The paper itself

Abstract

Tumor cells with heterogeneity and diversity can express different markers. At present, positive separation of circulating tumor cells (CTC) taking EpCAM as the marker was used in most cases which could be one-sided, while this study successfully prepared four antibody-modified magnetic immunoliposomes (MIL) by using the self-assembled liposome with antibody derivatives. This study aims to explore the separation efficiency and clinical detection feasibility of single or combined use of MIL with multi-tumor markers on different tumors. Captured CTC were stained with CK-FITC, CD45-PE and DAPI, and fluorescence microscope was used for the observation, analysis and calculation. The result indicated that the CTC number positive rate in blood samples of four different magnetic balls on the same patient could be up to 87.5% in 32 patients with 14 different kinds tumors. While the effect of directly mixed separation by four kinds of magnetic balls was not satisfying. It suggested that the MIL of multi-tumor markers could be a powerful tool for CTC separation in application of tumor screening and prognosis.

Indexed as

AnimalsBiomarkers, TumorCell Line, TumorCell SeparationEpithelial Cell Adhesion MoleculeHumansMagnetite NanoparticlesNeoplasmsNeoplastic Cells, CirculatingBiomarkers, TumorEpithelial Cell Adhesion MoleculeMagnetite NanoparticlesCirculating tumor cellClinical verificationsEpithelial cell adhesion moleculeMagnetic immunoliposomes

Identifiers

PMID31767014
PMCPMC6876097
OpenAlexW2989691932

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.