Evidence map›Paper›PMID 28301261›Full record

ArticleCancer biotherapy & radiopharmaceuticals2017

A Radiolabeled Fully Human Antibody to Human Aspartyl (Asparaginyl) β-Hydroxylase Is a Promising Agent for Imaging and Therapy of Metastatic Breast Cancer.

Ekaterina Revskaya, Zewei Jiang, Alfred Morgenstern, Frank Bruchertseifer, Muctarr Sesay, Susan Walker, Steven Fuller, Michael S Lebowitz, Claudia Gravekamp, Hossein A Ghanbari and 1 more

Abstract read
In one paragraph

Article in Cancer biotherapy & radiopharmaceuticals, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Aspartate β-hydroxylase as a target for cancer therapy.Journal of experimental & clinical cancer research : CR · 2020
    Review
  9. Radiolabelled Aptamers for Theranostic Treatment of Cancer.Pharmaceuticals (Basel, Switzerland) · 2018
    Review
  10. Review
  11. Drug conjugates-an emerging approach to treat breast cancer.Pharmacology research & perspectives · 2018
    Review
  12. 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

11 authors at 2 institutions in 2 countries.

Ekaterina Revskaya1 Department of Radiology, Albert Einstein College of Medicine , Bronx, New York.
Zewei Jiang1 Department of Radiology, Albert Einstein College of Medicine , Bronx, New York.
Alfred Morgenstern2 European Commission, Joint Research Centre , Directorate for Nuclear Safety and Security, Karlsruhe, Germany .
Frank Bruchertseifer2 European Commission, Joint Research Centre , Directorate for Nuclear Safety and Security, Karlsruhe, Germany .
Muctarr Sesay3 Goodwin Biotechnology , Plantation, Florida.
Susan Walker4 Panacea Pharmaceuticals , Gaithersburg, Maryland.
Steven Fuller4 Panacea Pharmaceuticals , Gaithersburg, Maryland.
Michael S Lebowitz4 Panacea Pharmaceuticals , Gaithersburg, Maryland.
Claudia Gravekamp1 Department of Radiology, Albert Einstein College of Medicine , Bronx, New York.
Hossein A Ghanbari4 Panacea Pharmaceuticals , Gaithersburg, Maryland.
Ekaterina Dadachova1 Department of Radiology, Albert Einstein College of Medicine , Bronx, New York.
Albert Einstein College of Medicine · USJoint Research Centre · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a need for novel effective and safe therapies for metastatic breast cancer based on targeting tumor-specific molecular markers of cancer. Human aspartyl (asparaginyl) β-hydroxylase (HAAH) is a highly conserved enzyme that hydroxylates epidermal growth factor-like domains in transformation-associated proteins and is overexpressed in a variety of cancers, including breast cancer. A fully human monoclonal antibody (mAb) PAN-622 has been developed to HAAH. In this study, they describe the development of PAN-622 mAb as an agent for imaging and radioimmunotherapy of metastatic breast cancer. PAN-622 was conjugated to several ligands such as DOTA, CHXA″, and DTPA to enable subsequent radiolabeling and its immunoreactivity was evaluated by an HAAH-specific enzyme-linked immunosorbent assay and binding to the HAAH-positive cells. As a result, DTPA-PAN-622 was chosen to investigate biodistribution in healthy CD-1 female mice and 4T1 mammary tumor-bearing BALB/c mice. The

Indexed as

AnimalsAntibodies, MonoclonalBreast NeoplasmsCell Line, TumorDiagnostic ImagingEnzyme-Linked Immunosorbent AssayFemaleHumansLigandsMiceMice, Inbred BALB CMixed Function OxygenasesNeoplasm MetastasisRadioimmunotherapyTissue DistributionAntibodies, Monoclonalaspartic acid 2-oxoglutarate-dependent dioxygenaseLigandsMixed Function Oxygenases111In213BiHAAHmetastatic breast cancerPAN-622 human antibodyradioimmunotherapy

Identifiers

PMID28301261
PMCPMC5361764
OpenAlexW2595200215

What OpenQuestion holds

Textmetadata
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.