Evidence map›Paper›PMID 34369155›Full record

ArticleACS chemical biology2021

Combined Effect of Anti-SSEA4 and Anti-Globo H Antibodies on Breast Cancer Cells.

Ruey-Herng Lee, Yu-Jen Wang, Ting-Yen Lai, Tsui-Ling Hsu, Po-Kai Chuang, Han-Chung Wu, Chi-Huey Wong

Abstract read
In one paragraph

Article in ACS chemical biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Impacts of Globo H Ceramide on Tumor Microenvironment.Advances in experimental medicine and biology · 2026
    Review
  3. Article
  4. Increased expression of SSEA-4 on TKI-resistant non-small cell lung cancer with EGFR-T790M mutation.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  5. Article
  6. Review
  7. Study on antibody Fc-glycosylation for optimal effector functions.Chemical communications (Cambridge, England) · 2023
    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

7 authors.

Ruey-Herng LeeGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.
Yu-Jen WangGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.
Ting-Yen LaiGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.
Tsui-Ling HsuGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.
Po-Kai ChuangDepartment of Chemistry, The Scripps Research Institute, La Jolla, California 92037, United States.
Han-Chung WuInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei 115, Taiwan.
Chi-Huey WongGenomics Research Center, Academia Sinica, Taipei 115, Taiwan.ORCID 0000-0002-9961-7865

Funding

Targeting Influenza A Virus by a Carbohydrate-inspired StrategyR01AI130227 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI CHI-HUEY WONG · 2019 to 2026
$3.3M
NIAID NIH HHS R01 AI130227
6 · The paper itself

Abstract

The globo-series glycosphingolipids (SSEA3, SSEA4, and Globo H) were shown to express in many cancers selectively, and a combination of anti-SSEA4 and anti-Globo H antibodies was able to suppress tumor growth in mice inoculated with breast cancer cell lines. To further understand the effect, we focused on the combined effect of the two antibodies in target binding and antibody-dependent cellular cytotoxicity (ADCC) in vitro. Here, we report that the binding of anti-Globo H antibody (VK9) to MDA-MB231 breast cancer cells was influenced by anti-SSEA4 antibody (MC813-70), and a combination of both antibodies induced a similar effect as did anti-SSEA4 antibodies alone in a reporter-based ADCC assay, indicating that SSEA4 is a major target in breast cancer due to its higher expression than Globo H. Furthermore, we showed that a homogeneous anti-SSEA4 antibody (chMC813-70-SCT) designed to maximize the ADCC activity can be used to isolate a subpopulation of natural killer (NK) cells that exhibit an ∼23% increase in killing the target cells as compared to the unseparated NK cells. These findings can be used to predict a therapy outcome based on the expression levels of antigens and evaluate therapeutic antibody development.

Indexed as

AnimalsAntibodiesAntigens, Tumor-Associated, CarbohydrateBreast NeoplasmsCell Line, TumorHumansKiller Cells, NaturalMiceReceptors, IgGStage-Specific Embryonic AntigensAntibodiesAntigens, Tumor-Associated, CarbohydrateFCGR3A protein, humanGlobo-HReceptors, IgGstage-specific embryonic antigen-4Stage-Specific Embryonic Antigens

Identifiers

PMID34369155
PMCPMC8423375

What OpenQuestion holds

Textmetadata
LicenceTDM
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.