Evidence map›Paper›PMID 25699098›Full record

ArticleTheranostics2015

Small sized EGFR1 and HER2 specific bifunctional antibody for targeted cancer therapy.

Li Ding, Caiping Tian, Song Feng, Guissi Fida, Congying Zhang, Yuxiang Ma, Guanhua Ai, Samuel Achilefu, Yueqing Gu

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 3% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Advances in Nanobody-Based Platforms for Precision Cancer Diagnosis and Therapy.Polymer science & technology (Washington, D.C.) · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Broad-Spectrum Engineered Multivalent Nanobodies Against SARS-CoV-1/2.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  10. Article
  11. Article
  12. NANOBODYInternational journal of molecular sciences · 2023
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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 2 countries.

Li Ding1. Department of Biomedical Engineering, China Pharmaceutical University, School of Life Science and Technology, Nanjing, China.
Caiping Tian1. Department of Biomedical Engineering, China Pharmaceutical University, School of Life Science and Technology, Nanjing, China.
Song Feng1. Department of Biomedical Engineering, China Pharmaceutical University, School of Life Science and Technology, Nanjing, China.
Guissi Fida1. Department of Biomedical Engineering, China Pharmaceutical University, School of Life Science and Technology, Nanjing, China.
Congying Zhang1. Department of Biomedical Engineering, China Pharmaceutical University, School of Life Science and Technology, Nanjing, China.
Yuxiang Ma1. Department of Biomedical Engineering, China Pharmaceutical University, School of Life Science and Technology, Nanjing, China.
Guanhua Ai1. Department of Biomedical Engineering, China Pharmaceutical University, School of Life Science and Technology, Nanjing, China.
Samuel Achilefu2. Department of Radiology, Washington University, School of Medicine, St. Louis, USA.
Yueqing Gu1. Department of Biomedical Engineering, China Pharmaceutical University, School of Life Science and Technology, Nanjing, China.
China Pharmaceutical University · CNWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeting tumors using miniature antibodies is a novel and attractive therapeutic approach, as these biomolecules exhibit low immunogenicity, rapid clearance, and high targeting specificity. However, most of the small-sized antibodies in existence do not exhibit marked anti-tumor effects, which limit their use in targeted cancer immunotherapy. To overcome this difficulty in targeting multiple biomarkers by combination therapies, we designed a new bifunctional antibody, named MaAbNA (multivalent antibody comprised of nanobody and affibody moieties), capable of targeting EGFR1 and HER2, which are widely overexpressed in a variety of tumor types. The small-sized (29 kDa) MaAbNA, which was expressed in E.coli, consists of one anti-EGFR1 nanobody and two anti-HER2 affibodies, and possesses high affinity (KD) for EGFR1 (~4.1 nM) and HER2 (~4.7 nM). In order to enhance its anti-tumor activity, MaAbNA was conjugated with adriamycin (ADM) using a PEG2000 linker, forming a new complex anticancer drug, MaAbNA-PEG2000-ADM. MaAbNA exhibited high inhibitory effects on tumor cells over-expressing both EGFR1 and HER2, but displayed minimal cytotoxicity in cells expressing low levels of EGFR1 and HER2. Moreover, MaAbNA-PEG2000-ADM displayed increased tumoricidal effects than ADM or MaAbNA alone, as well exhibited greater antitumor efficacy than EGFR1 (Cetuximab) and HER2 (Herceptin) antibody drugs. The ability of MaAbNA to regulate expression of downstream oncogenes c-jun, c-fos, c-myc, as well as AEG-1 for therapeutic potential was evaluated by qPCR and western-blot analyses. The antitumor efficacy of MaAbNA and its derivative MaAbNA-PEG2000-ADM were validated in vivo, highlighting the potential for use of MaAbNA as a highly tumor-specific dual molecular imaging probe and targeted cancer therapeutic.

Indexed as

AnimalsAntibodies, BispecificCell Line, TumorCell ProliferationCell SurvivalDisease Models, AnimalErb-b2 Receptor Tyrosine KinasesErbB ReceptorsEscherichia coliGene ExpressionGene Expression ProfilingHumansImmunotherapyMiceNeoplasmsRecombinant Fusion ProteinsAntibodies, BispecificEGFR protein, humanERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesErbB ReceptorsRecombinant Fusion ProteinsSingle-Domain AntibodiesEGFR1HER2

Identifiers

PMID25699098
PMCPMC4329502
OpenAlexW2137170183

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.