Evidence map›Paper›PMID 26571416›Full record

ArticlePloS one2015

Immuno-PET Imaging of HER3 in a Model in which HER3 Signaling Plays a Critical Role.

Qinghua Yuan, Takako Furukawa, Takahiro Tashiro, Kouki Okita, Zhao-Hui Jin, Winn Aung, Aya Sugyo, Kotaro Nagatsu, Hiroko Endo, Atsushi B Tsuji and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. HER3 PET Imaging:Cancers · 2021
    Article
  7. PET and SPECT Imaging of the EGFR Family (RTK Class I) in Oncology.International journal of molecular sciences · 2021
    Review
  8. The Radiolabeled HER3 Targeting Molecules for Tumor Imaging.Iranian journal of pharmaceutical research : IJPR · 2021
    Review
  9. Article
  10. Imaging EGFR and HER3 throughScientific reports · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. mAbs
    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

15 authors at 2 institutions in 1 country.

Qinghua YuanMolecular Imaging Center, National Institute of Radiological Sciences, Chiba, Japan.
Takako FurukawaMolecular Imaging Center, National Institute of Radiological Sciences, Chiba, Japan.
Takahiro TashiroDepartment of Biochemistry, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka, Japan.
Kouki OkitaCell Biology Laboratory, Department of Pharmaceutical Sciences, School of Pharmacy, Kinki University, Higashi Osaka, Japan.
Zhao-Hui JinMolecular Imaging Center, National Institute of Radiological Sciences, Chiba, Japan.
Winn AungMolecular Imaging Center, National Institute of Radiological Sciences, Chiba, Japan.
Aya SugyoMolecular Imaging Center, National Institute of Radiological Sciences, Chiba, Japan.
Kotaro NagatsuMolecular Imaging Center, National Institute of Radiological Sciences, Chiba, Japan.
Hiroko EndoDepartment of Biochemistry, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka, Japan.
Atsushi B TsujiMolecular Imaging Center, National Institute of Radiological Sciences, Chiba, Japan.
Ming-Rong ZhangMolecular Imaging Center, National Institute of Radiological Sciences, Chiba, Japan.
Takashi MasukoCell Biology Laboratory, Department of Pharmaceutical Sciences, School of Pharmacy, Kinki University, Higashi Osaka, Japan.
Masahiro InoueDepartment of Biochemistry, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka, Japan.
Yasuhisa FujibayashiMolecular Imaging Center, National Institute of Radiological Sciences, Chiba, Japan.
Tsuneo SagaMolecular Imaging Center, National Institute of Radiological Sciences, Chiba, Japan.
Osaka Medical Center for Cancer and Cardiovascular Diseases · JPKindai University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HER3 is overexpressed in various carcinomas including colorectal cancer (CRC), which is associated with poor prognosis, and is involved in the development of therapy resistance. Thus, an in vivo imaging technique is needed to evaluate the expression of HER3, an important therapeutic and diagnostic target. Here, we report successful HER3 PET imaging using a newly generated anti-human HER3 monoclonal antibody, Mab#58, and a mouse model of a HER3-overexpressing xenograft tumor. Furthermore, we assessed the role of HER3 signaling in CRC cancer tissue-originated spheroid (CTOS) and applied HER3 imaging to detect endogenous HER3 in CTOS-derived xenografts. Cell binding assays of 89Zr-labeled Mab#58 using the HER3-overexpressing cell line HER3/RH7777 demonstrated that [89Zr]Mab#58 specifically bound to HER3/RH7777 cells (Kd = 2.7 nM). In vivo biodistribution study in mice bearing HER3/RH7777 and its parent cell xenografts showed that tumor accumulation of [89Zr]Mab#58 in HER3/RH7777 xenografts was significantly higher than that in the control from day 1 to day 4, tending to increase from day 1 to day 4 and reaching 12.2 ± 4.5%ID/g. Radioactivity in other tissues, including the control xenograft, decreased or remained unchanged from day 1 to day 6. Positron emission tomography (PET) in the same model enabled clear visualization of HER3/RH7777 xenografts but not of RH7777 xenografts. CTOS growth assay and signaling assay revealed that CRC CTOS were dependent on HER3 signaling for their growth. In PET studies of mice bearing a CRC CTOS xenograft, the tumor was clearly visualized with [89Zr]Mab#58 but not with the 89Zr-labeled control antibody. Thus, tumor expression of HER3 was successfully visualized by PET with 89Zr-labeled anti-HER3 antibody in CTOS xenograft-bearing mice, a model that retains the properties of the patient tumor. Non-invasive targeting of HER3 by antibodies is feasible, and it is expected to be useful for cancer diagnosis and treatment.

Indexed as

AnimalsCell Line, TumorFemaleFluoroimmunoassayHumansMice, Inbred BALB CMice, NudeNeoplasm TransplantationOrgan SpecificityPositron-Emission TomographyRatsReceptor, ErbB-3Signal TransductionSpheroids, CellularERBB3 protein, humanReceptor, ErbB-3

Identifiers

PMID26571416
PMCPMC4646434
OpenAlexW2174304850

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.