Evidence map›Paper›PMID 16341531›Full record

ArticleCancer immunology, immunotherapy : CII2006

The in vitro antitumor effect and in vivo tumor-specificity distribution of human-mouse chimeric antibody against transferrin receptor.

Ye Qing, Wang Shuo, Wang Zhihua, Zhu Huifen, Lei Ping, Liu Lijiang, Zhao Xiaorong, Chao Liming, Xiao Daiwen, Huang Yu and 4 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  13. Iron in multiple myeloma.Critical reviews in oncogenesis · 2013
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Preparation and identification of scFv and bsFv against transferrin receptor.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2008
    Article
  19. Review
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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

14 authors at 3 institutions in 1 country.

Ye QingLaboratory of Molecular and Immuno-Pharmacology, Department of Pharmacology and Immunology, Tongji Medical College, Huazhong University of Science and Technology, No. 13, Hongkong Road, 430030 Wuhan, People's Republic of China.
Wang Shuo
Wang Zhihua
Zhu Huifen
Lei Ping
Liu Lijiang
Zhao Xiaorong
Chao Liming
Xiao Daiwen
Huang Yu
Xing Wei
Fang Min
Feng Zuohua
Shen Guanxin
Huazhong University of Science and Technology · CNJianghan University · CNTongji Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transferrin receptor (TfR/CD71) deserves attention as a selective target for cancer therapy due to its higher expression in tumors versus normal tissues. Also, it has been shown the mouse-derived monoclonal antibody against TfR can significantly inhibit the proliferation of tumor cells. Through constructing the chimeric antibody against TfR, the antigenicity of antibody can be weakened, and most importantly, the antitumor effect of antibody can be strengthened by the introduction of the human Fc fragment. In previous studies, we successfully constructed the human-mouse chimeric antibody against TfR (D2C) and demonstrated that its Fab fragment could specially recognize the TfR on the surface of target cells. In this study, through labeling the chimeric antibody D2C with 125I, we calculated the affinity constant (Ka) of 9.34-9.62x10(9) l/mol for this antibody according to the Scatchard drawing method. Moreover, in vivo studies in nude mice-bearing human liver cancer (SMMC-7721) xenografts have shown that the radioactivity distribution ratio of 131I-D2C on T/NT was 2-14:1 or 3-21:1 on the seventh day after intraperitoneal or intratumoral injection of 131I-labeled D2C (131I-D2C). These evidences indicated that the in vivo distribution of D2C display the characteristics of certain tumor-specificity localization. In vitro studies, D2C can induce the apoptosis of K562 through the mitochondria death pathway and arrest the cell at G1 phase, as determined by cell cycle analysis. Using the human tumor cells (K562, CEM, and SMMC-7721) expressing TfR as target cells, and normal human PBMC as effector cells, Fc fragment of D2C can perform both the antibody-dependent cell-mediated cytotoxicity and the complement-dependent cytotoxicity. Together, it was demonstrated that the D2C display a tumor-specificity distribution, and has a strong antitumor effect. Thus, it has the potential therapeutic significance.

Indexed as

AnimalsAntibodies, MonoclonalAntigens, CDAntineoplastic AgentsApoptosisBinding, CompetitiveBinding Sites, AntibodyCaspase 8CaspasesCell Cycle ProteinsCell Line, TumorCell SurvivalCytochromes cDrug Screening Assays, AntitumorFlow CytometryHumansAntibodies, MonoclonalAntigens, CDAntineoplastic AgentsCASP8 protein, humanCasp8 protein, mouseCaspase 8CaspasesCD71 antigenCell Cycle ProteinsCytochromes cImmunoglobulin Fab FragmentsReceptors, TransferrinRecombinant Fusion Proteins

Identifiers

PMID16341531
PMCPMC11030686
OpenAlexW2081240241

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.