Evidence map›Paper›PMID 29854844›Full record

ArticleJournal of immunology research2018

A Novel Bimodal Imaging Agent Targeting HER2 Molecule of Breast Cancer.

Wei Lv, Yamei Shen, Hengli Yang, Rui Yang, Wenbin Cai, Jian Zhang, Lijun Yuan, Yunyou Duan, Li Zhang

Open access · goldAbstract read
In one paragraph

Article in Journal of immunology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Molecular Ultrasound Imaging.Nanomaterials (Basel, Switzerland) · 2020
    Review
  5. Article
  6. 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

9 authors at 2 institutions in 1 country.

Wei LvDepartment of Ultrasound Diagnosis, Tang Du Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, China.
Yamei ShenDepartment of Ultrasound Diagnosis, Tang Du Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, China.
Hengli YangDepartment of Ultrasound Diagnosis, Tang Du Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, China.
Rui YangDepartment of Ultrasound Diagnosis, Tang Du Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, China.
Wenbin CaiDepartment of Ultrasound Diagnosis, Tang Du Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, China.
Jian ZhangState Key Laboratory of Cancer Biology, Department of Biochemistry and Molecular Biology, Fourth Military Medical University, Xi'an, Shaanxi 710032, China.ORCID 0000-0001-8338-9426
Lijun YuanDepartment of Ultrasound Diagnosis, Tang Du Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, China.
Yunyou DuanDepartment of Ultrasound Diagnosis, Tang Du Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, China.ORCID 0000-0003-0769-8328
Li ZhangDepartment of Ultrasound Diagnosis, Tang Du Hospital, Fourth Military Medical University, Xi'an, Shaanxi 710038, China.ORCID 0000-0001-8719-4407
Tang Du Hospital · CNAir Force Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nanobubble (NB), a newly developed nanoscaled ultrasound contrast agent (UCA) for molecular imaging, has been widely researched for these years. Targeting it with functional molecule, nanobubble can adhere selectively to cellular epitopes and receptors outside the vasculature via enhanced permeability and retention (EPR) effect of tumor blood vessel. To enhance the targeting rate of our previous prepared NBs-Affibody for HER2 (+) breast cancer imaging, we introduced a near-infrared fluorescent (NIRF) dye, IR783, in this study to enhance tumor-specific targeting rate and provide a promising modality for dual-mode imaging. The prepared IR783-NBs-Affibody presented a uniform nanoscale size around 482.7 ± 54.3 nm, good biosecurity, and stability over time. The encapsulation efficiency (EE) of IR-783 was 15.09% in the conjugates leading to a successful NIR fluorescence and ultrasound enhancement imaging ex vivo. IR783-NBs-Affibody was able to automatically accumulate on BT474 cells with a highly increased targeting rate of 85.4% compared with previous NBs-Affibody of 26.6%, while Affibody-guided HER2 binding was only found in HER2-positive cell lines (BT474 and T-47D). The newly developed IR783-NBs-Affibody is characterized with favorable HER2 targeting ability and bimodal imaging capability for breast cancer. Thus, IR783-NBs-Affibody holds great potential in molecular diagnosis for patients with breast cancer.

Indexed as

AntibodiesBreast NeoplasmsCell Line, TumorContrast MediaErb-b2 Receptor Tyrosine KinasesFemaleFluorescent DyesHumansMolecular Diagnostic TechniquesNanocapsulesRecombinant Fusion ProteinsUltrasonographyAntibodiesContrast MediaERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesFluorescent DyesNanocapsulesRecombinant Fusion Proteins

Identifiers

PMID29854844
PMCPMC5944285
OpenAlexW2791943371

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.