Evidence map›Paper›PMID 30188117›Full record

ArticleACS applied materials & interfaces2018

P-Glycoprotein-Targeted Photothermal Therapy of Drug-Resistant Cancer Cells Using Antibody-Conjugated Carbon Nanotubes.

Xubin Suo, Brittany N Eldridge, Han Zhang, Chengqiong Mao, Yuanzeng Min, Yao Sun, Ravi Singh, Xin Ming

Open access · greenAbstract read
In one paragraph

Article in ACS applied materials & interfaces, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
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  7. Recent Advances in Carbon-Based Electrodes for Energy Storage and Conversion.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
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  14. Nanostructures as Photothermal Agents in Tumor Treatment.Molecules (Basel, Switzerland) · 2022
    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

8 authors at 3 institutions in 2 countries.

Xubin SuoSchool of Pharmacy , Guangdong Pharmaceutical University , Guangzhou , Guangdong 510006 , China.
Brittany N Eldridge
Han ZhangSchool of Traditional Chinese Medicine , Guangdong Pharmaceutical University , Guangzhou 510006 , China.
Yuanzeng MinDepartment of Chemistry , University of Science and Technology of China , Hefei 230000 , Anhui , China.
Yao Sun
Wake Forest University · USGuangdong Pharmaceutical University · CNUniversity of Science and Technology of China · CN

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
Development of a novel therapeutic agent that exploits specific vulnerabilities in claudin low breast cancerR01CA207222 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SINGH, RAVI N · 2017 to 2021
$1.7M
Combination Therapy of OvCA with Oligonucleotides and Photodynamic TherapyR01CA194064 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI MING, XIN · 2016 to 2020
$1.4M
NCI NIH HHS P30 CA012197NCI NIH HHS R01 CA194064NCI NIH HHS R01 CA207222
6 · The paper itself

Abstract

P-Glycoprotein (Pgp)-medicated multidrug resistance (MDR) remains a formidable challenge to cancer therapy. As conventional approaches using small-molecule inhibitors failed in clinical development because of the lack of cancer specificity, we develop Pgp-targeted carbon nanotubes to achieve highly cancer-specific therapy through combining antibody-based cancer targeting and locoregional tumor ablation with photothermal therapy. Through a dense coating with phospholipid-poly(ethylene glycol), we have engineered multiwalled carbon nanotubes (MWCNTs) which show minimum nonspecific cell interactions and maximum intercellular diffusion. After chemically modifying with an anti-Pgp antibody, these MWCNTs showed highly Pgp-specific cellular uptake. Treatment of the targeted MWCNTs caused dramatic cytotoxicity in MDR cancer cells upon photoirradiation, whereas they did not cause any toxicity in the dark or phototoxicity toward normal cells that do not express Pgp. Because of excellent intratumor diffusion and Pgp-specific cellular uptake, the targeted MWCNTs produced strong phototoxicity in tumor spheroids of MDR cancer cells, a 3-D tumor model for studying tumor penetration and therapy. In conclusion, we have developed highly Pgp-specific MWCNTs that may provide an effective therapy for MDR cancers where other approaches have failed.

Indexed as

AnimalsATP Binding Cassette Transporter, Subfamily B, Member 1Cell LineDrug Resistance, MultipleDrug Resistance, NeoplasmFlow CytometryMiceNanotubes, CarbonPhospholipidsPhotochemotherapyPolyethylene GlycolsSpheroids, CellularATP Binding Cassette Transporter, Subfamily B, Member 1Nanotubes, CarbonPhospholipidsPolyethylene Glycolscancer multidrug resistancecancer targetingcarbon nanotubesP-glycoproteinphotothermal therapy

Identifiers

PMID30188117
PMCPMC6200400
OpenAlexW2889632874

What OpenQuestion holds

Textmetadata
LicenceTDM
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.