Evidence map›Paper›PMID 36678740›Full record

ArticlePharmaceutics2022

Targeting EGFR and Monitoring Tumorigenesis of Human Lung Cancer Cells In Vitro and In Vivo Using Nanodiamond-Conjugated Specific EGFR Antibody.

Yu-Wei Lin, Hung-Cheng Su, Emmanuel Naveen Raj, Kuang-Kai Liu, Chien-Jen Chang, Tzu-Chia Hsu, Po-Yun Cheng, Rou-Hsin Wang, Yen-Her Lai, Chien-Hung Chen and 2 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
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 1 institution in 1 country.

Yu-Wei LinDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Hung-Cheng SuDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Emmanuel Naveen RajInstitute of Molecular Medicine and Bioengineering, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.ORCID 0000-0002-7445-9354
Kuang-Kai LiuDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Chien-Jen ChangDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.ORCID 0000-0001-7700-1325
Tzu-Chia HsuDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Po-Yun ChengDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Rou-Hsin WangDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Yen-Her LaiInstitute of Molecular Medicine and Bioengineering, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Chien-Hung ChenDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Yen-Cheng LinDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
Jui-I ChaoDepartment of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu 30068, Taiwan.
National Yang Ming Chiao Tung University · TW

Funding

Ministry of Science and Technology 111-2731-M-009-001Ministry of Science and Technology MOST 109-2320-B-009-003-MY3Taipei Veterans General Hospital VGHUST111-G1-5-3
6 · The paper itself

Abstract

Nanoprobes provide advantages for real-time monitoring of tumor markers and tumorigenesis during cancer progression and development. Epidermal growth factor receptor (EGFR) is a key protein that plays crucial roles for tumorigenesis and cancer therapy of lung cancers. Here, we show a carbon-based nanoprobe, nanodiamond (ND), which can be applied for targeting EGFR and monitoring tumorigenesis of human lung cancer cells in vitro and in vivo. The optimal fluorescent intensities of ND particles were observed in the human lung cancer cells and nude mice under in vivo imaging system. The fluorescence signal of ND particles can be real-time detected in the xenografted human lung tumor formation of nude mice. Moreover, the ND-conjugated specific EGFR antibody cetuximab (Cet) can track the location and distribution of EGFR proteins of lung cancer cells in vitro and in vivo. ND-Cet treatment increased cellular uptake ability of nanocomposites in the EGFR-expressed cells but not in the EGFR-negative lung cancer cells. Interestingly, single ND-Cet complex can be directly observed on the protein G bead by immunoprecipitation and confocal microscopy. Besides, the EGFR proteins were transported to lysosomes for degradation. Together, this study demonstrates that ND-conjugated Cet can apply for targeting EGFR and monitoring tumorigenesis during lung cancer progression and therapy.

Indexed as

cetuximabEGFRlung cancer therapynanodiamondtumorigenesis

Identifiers

PMID36678740
PMCPMC9865332
OpenAlexW4313238215

What OpenQuestion holds

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LicenceCC BY
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.