Evidence map›Paper›PMID 32240054›Full record

ArticleCancer biology & therapy2020

A novel targeted GPC3/CD3 bispecific antibody for the treatment hepatocellular carcinoma.

Lin Yu, Xi Yang, Nan Huang, Qiao-Li Lang, Qi-Lin He, Wang Jian-Hua, Ge Liang-Peng

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Emerging Immune-Based Therapeutic Strategies in Hepatocellular Carcinoma.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Review
  3. Review
  4. Review
  5. Review
  6. Navigating second-line therapy after immunotherapy in advanced HCC☆.JHEP reports : innovation in hepatology · 2026
    Review
  7. Review
  8. Review
  9. Review
  10. Immunotherapy for hepatocellular carcinoma.JHEP reports : innovation in hepatology · 2024
    Review
  11. Article
  12. Evolving therapeutic landscape of advanced hepatocellular carcinoma.Nature reviews. Gastroenterology & hepatology · 2023
    Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. A bispecific antibody targeting GPC3 and CD47 induced enhanced antitumor efficacy against dual antigen-expressing HCC.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  19. Review
  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

7 authors at 2 institutions in 1 country.

Lin YuKey Laboratory of Biorheological Science and Technology (Ministry of Education), College of Bioengineering, Chongqing University , Chongqing, China.
Xi YangDepartment of Bioengineering, Chongqing Academy of Animal Sciences , Chongqing, China.
Nan HuangDepartment of Bioengineering, Chongqing Academy of Animal Sciences , Chongqing, China.
Qiao-Li LangDepartment of Bioengineering, Chongqing Academy of Animal Sciences , Chongqing, China.
Qi-Lin HeDepartment of Bioengineering, Chongqing Academy of Animal Sciences , Chongqing, China.
Wang Jian-HuaKey Laboratory of Biorheological Science and Technology (Ministry of Education), College of Bioengineering, Chongqing University , Chongqing, China.
Ge Liang-PengDepartment of Bioengineering, Chongqing Academy of Animal Sciences , Chongqing, China.
Chongqing Academy of Animal Science · CNChongqing University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the most frequent primary liver cancer but has shown limited success to date in the treatment of advanced stage. Recruitment of T cells for cancer treatment is a rapidly growing strategy in immunotherapy such as chimeric antigen receptor T cells and bispecific antibodies. However, unwanted aggregations, structural instability or short serum half-life are major challenges of bispecific antibodies. Here, we developed a new format of T cell-redirecting antibody that is bispecific for membrane proteoglycans GPC3 of HCC and the T-cell-specific antigen CD3, which demonstrated to be favorable stability and productivity. Cross-linking of T cells with GPC3 positive tumor cells by the anti-GPC3/CD3 bispecific antibody-mediated potent GPC3-dependent and concentration-dependent cytotoxicity in vitro. Administration of the bispecific antibody with different concentrations in murine xenograft models of human HCC significantly inhibited tumor growth. In addition, no effects on tumor growth were observed in the absence of human effector cells or the bispecific antibody. Taken together, the anti-GPC3/CD3 bispecific antibody might be a potential therapeutic treatment for HCC.

Indexed as

AnimalsAntibodies, BispecificCarcinoma, HepatocellularFemaleGlypicansHumansImmunotherapyLiver NeoplasmsMiceMice, Inbred NODAntibodies, BispecificGlypicansGPC3 protein, mouseBispecific antibodyGPC3hepatocellular carcinomaimmunotherapyT-cell recruitment

Identifiers

PMID32240054
PMCPMC7515540
OpenAlexW3014527710

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.