Evidence map›Paper›PMID 29568351›Full record

ArticleOncotarget2018

Targeting of embryonic annexin A2 expressed on ovarian and breast cancer by the novel monoclonal antibody 2448.

Simeon Cua, Heng Liang Tan, Wey Jia Fong, Angela Chin, Ally Lau, Vanessa Ding, Zhiwei Song, Yuansheng Yang, Andre Choo

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

18 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
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  5. Review
  6. Article
  7. Review
  8. Human colorectal cancer-associated carbohydrate antigen on annexin A2 protein.Journal of molecular medicine (Berlin, Germany) · 2021
    Article
  9. Annexin Animal Models-From Fundamental Principles to Translational Research.International journal of molecular sciences · 2021
    Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
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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

9 authors at 2 institutions in 1 country.

Simeon CuaStem Cells 1 Group, Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (ASTAR), Singapore 138668, Singapore.
Heng Liang TanStem Cells 1 Group, Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (ASTAR), Singapore 138668, Singapore.
Wey Jia FongStem Cells 1 Group, Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (ASTAR), Singapore 138668, Singapore.
Angela ChinStem Cells 1 Group, Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (ASTAR), Singapore 138668, Singapore.
Ally LauProteomics Group, Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (ASTAR), Singapore 138668, Singapore.
Vanessa DingStem Cells 1 Group, Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (ASTAR), Singapore 138668, Singapore.
Zhiwei SongExpression Engineering 1 Group, Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (ASTAR), Singapore 138668, Singapore.
Yuansheng YangAnimal Cell Technology 1 Group, Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (ASTAR), Singapore 138668, Singapore.
Andre ChooStem Cells 1 Group, Bioprocessing Technology Institute (BTI), Agency for Science, Technology and Research (ASTAR), Singapore 138668, Singapore.
Bioprocessing Technology Institute · SGAgency for Science, Technology and Research · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monoclonal antibodies (mAbs) play an increasingly important role in cancer therapy. To address the wide heterogeneity of the disease, the identification of novel antigen targets and the development of mAbs against them are needed. Our lab previously generated a panel of mAbs against human embryonic stem cells (hESC) using a whole cell immunization approach in mice. These mAbs can potentially target oncofetal antigens and be repurposed for antibody or antibody drug conjugate (ADC) therapy. From this panel, the novel IgG1 2448 was found to bind surface antigens on hESC and multiple cancer cell lines. Here, we show 2448 targets a unique glycan epitope on annexin A2 (ANXA2) and can potentially monitor the Epithelial-Mesenchymal Transition (EMT) in ovarian and breast cancer. To evaluate 2448 as a potential drug, 2448 was engineered and expressed as a chimeric IgG1. Chimeric 2448 (ch2448) demonstrated efficient and specific killing when conjugated to cytotoxic payloads as an ADC. In addition, ch2448 elicited potent antibody-dependent cell-mediated cytotoxicity (ADCC) activity

Indexed as

annexin a2antibodyantibody-dependent cell-mediated cytotoxicityantibody drug conjugatenew targets

Identifiers

PMID29568351
PMCPMC5862572
OpenAlexW2784139266

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.