Evidence map›Paper›PMID 37217781›Full record

ReviewNature reviews. Cancer2023

Endocytosis in cancer and cancer therapy.

Blerida Banushi, Shannon R Joseph, Benedict Lum, Jason J Lee, Fiona Simpson

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 122 papers.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed
39.6field-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

122 citing papers in PubMed, 184 citations in OpenAlex.

  1. Review
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  3. Enhanced anticancer efficacy ofMaterials today. Bio · 2026
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62 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

5 authors at 1 institution in 1 country.

Blerida Banushi *Frazer Institute, University of Queensland, Woolloongabba, Queensland, Australia.ORCID 0000-0002-4314-8369
Shannon R Joseph *Frazer Institute, University of Queensland, Woolloongabba, Queensland, Australia.ORCID 0000-0003-3512-1809
Benedict LumFrazer Institute, University of Queensland, Woolloongabba, Queensland, Australia.ORCID 0000-0001-8198-5494
Jason J LeeFrazer Institute, University of Queensland, Woolloongabba, Queensland, Australia.ORCID 0000-0001-9160-8932
Fiona SimpsonFrazer Institute, University of Queensland, Woolloongabba, Queensland, Australia. f.simpson@uq.edu.au.ORCID 0000-0002-0271-781X
The University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endocytosis is a complex process whereby cell surface proteins, lipids and fluid from the extracellular environment are packaged, sorted and internalized into cells. Endocytosis is also a mechanism of drug internalization into cells. There are multiple routes of endocytosis that determine the fate of molecules, from degradation in the lysosomes to recycling back to the plasma membrane. The overall rates of endocytosis and temporal regulation of molecules transiting through endocytic pathways are also intricately linked with signalling outcomes. This process relies on an array of factors, such as intrinsic amino acid motifs and post-translational modifications. Endocytosis is frequently disrupted in cancer. These disruptions lead to inappropriate retention of receptor tyrosine kinases on the tumour cell membrane, changes in the recycling of oncogenic molecules, defective signalling feedback loops and loss of cell polarity. In the past decade, endocytosis has emerged as a pivotal regulator of nutrient scavenging, response to and regulation of immune surveillance and tumour immune evasion, tumour metastasis and therapeutic drug delivery. This Review summarizes and integrates these advances into the understanding of endocytosis in cancer. The potential to regulate these pathways in the clinic to improve cancer therapy is also discussed.

Indexed as

EndocytosisNeoplasmsHumansMembrane ProteinsReceptor Protein-Tyrosine KinasesSignal TransductionMembrane ProteinsReceptor Protein-Tyrosine Kinases

Identifiers

PMID37217781
OpenAlexW4377287007

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.