Evidence map›Paper›PMID 33790553›Full record

ReviewInternational journal of nanomedicine2021

Nanobody: A Small Antibody with Big Implications for Tumor Therapeutic Strategy.

Shuyang Sun, Ziqiang Ding, Xiaomei Yang, Xinyue Zhao, Minlong Zhao, Li Gao, Qu Chen, Shenxia Xie, Aiqun Liu, Shihua Yin and 2 more

Open access · goldAbstract readReview
In one paragraph

Review in International journal of nanomedicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
13.0field-weighted citation impact, top 1% 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

61 citing papers in PubMed, 130 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Nanobody-Conjugated Theranostic Prodrug Targeting αAdvanced healthcare materials · 2026
    Article
  5. Article
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1 more citing papers are in PubMed but not listed here.

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

12 authors at 2 institutions in 2 countries.

Shuyang SunInternational Nanobody Research Center, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.
Ziqiang DingInternational Nanobody Research Center, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.
Xiaomei YangInternational Nanobody Research Center, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.
Xinyue ZhaoInternational Nanobody Research Center, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.
Minlong ZhaoInternational Nanobody Research Center, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.
Li GaoInternational Nanobody Research Center, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.
Qu ChenInternational Nanobody Research Center, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.
Shenxia XieInternational Nanobody Research Center, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.
Aiqun LiuInternational Nanobody Research Center, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.
Shihua YinInternational Nanobody Research Center, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.ORCID 0000-0002-1184-1978
Zhiping XuAustralian Institute for Bioengineering and Nanotechnology, University of Queensland, St Lucia, QLD, 4072, Australia.
Xiaoling LuInternational Nanobody Research Center, Guangxi Medical University, Nanning, Guangxi, 530021, People's Republic of China.
Guangxi Medical University · CNThe University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of monoclonal antibody treatments for successful tumor-targeted therapies took several decades. However, the efficacy of antibody-based therapy is still confined and desperately needs further improvement. Nanobodies are the recombinant variable domains of heavy-chain-only antibodies, with many unique properties such as small size (~15kDa), excellent solubility, superior stability, ease of manufacture, quick clearance from blood, and deep tissue penetration, which gain increasing acceptance as therapeutical tools and are considered also as building blocks for chimeric antigen receptors as well as for targeted drug delivery. Thus, one of the promising novel developments that may address the deficiency of monoclonal antibody-based therapies is the utilization of nanobodies. This article provides readers the significant factors that the structural and biochemical properties of nanobodies and the research progress on nanobodies in the fields of tumor treatment, as well as their application prospect.

Indexed as

AnimalsClinical Trials as TopicCombined Modality TherapyDrug Delivery SystemsHumansNeoplasmsReceptors, Cell SurfaceSingle-Domain AntibodiesReceptors, Cell SurfaceSingle-Domain AntibodiesCAR-Tdrug deliveryimmunotherapynanobodytumor treatment

Identifiers

PMID33790553
PMCPMC7997558
OpenAlexW3136307594

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.