Evidence map›Paper›PMID 27284243›Full record

ArticleInternational journal of nanomedicine2016

Development of octreotide-conjugated polymeric prodrug of bufalin for targeted delivery to somatostatin receptor 2 overexpressing breast cancer in vitro and in vivo.

Tao Liu, Tingting Jia, Xia Yuan, Cheng Liu, Jian Sun, Zhenhua Ni, Jian Xu, Xuhui Wang, Yi Yuan

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
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  4. Combating Drug Resistance in Colorectal Cancer Using Herbal Medicines.Chinese journal of integrative medicine · 2021
    Review
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  6. Article
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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

9 authors at 1 institution in 1 country.

Tao LiuCentralab, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.
Tingting JiaDepartment of Pharmacy, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.
Xia YuanDepartment of Pharmacy, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.
Cheng LiuCentralab, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.
Jian SunCentralab, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.
Zhenhua NiCentralab, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.
Jian XuCentralab, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.
Xuhui WangDepartment of Pharmacy, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.
Yi YuanDepartment of Pharmacy, Putuo Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, People's Republic of China.
Shanghai University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDevelopment of polymeric prodrugs of small molecular anticancer drugs has become one of the most promising strategies to overcome the intrinsic shortcomings of small molecular anticancer drugs and improve their anticancer performance. MATERIALS AND

methodsIn the current work, we fabricated a novel octreotide (Oct)-modified esterase-sensitive tumor-targeting polymeric prodrug of bufalin (BUF) and explored its anticancer performance against somatostatin receptor 2 overexpressing breast cancer.

resultsThe obtained tumor-targeting polymeric prodrug of BUF, P(oligo[ethylene glycol] monomethyl ether methacrylate [OEGMA]-co-BUF-co-Oct), showed a nanosize dimension and controlled drug release features in the presence of esterase. It was demonstrated by in vitro experiment that P(OEGMA-co-BUF-co-Oct) showed enhanced cytotoxicity, cellular uptake, and apoptosis in comparison with those of free BUF. In vivo experiment further revealed the improved accumulation of drugs in tumor tissues and enhanced anticancer performance of P(OEGMA-co-BUF-co-Oct).

conclusionTaken together, this study indicated that polymeric prodrug of BUF holds promising potential toward the treatment of somatostatin receptor 2 overexpressing breast cancer.

Indexed as

AnimalsAntineoplastic AgentsApoptosisBreast NeoplasmsBufanolidesCell SurvivalDrug Delivery SystemsDrug LiberationEndocytosisFemaleFlow CytometryHumansHydrodynamicsMCF-7 CellsMethacrylatesMice, Inbred BALB CAntineoplastic AgentsbufalinBufanolidesMethacrylatesMicellesOctreotidePolymersProdrugsReceptors, Somatostatinsomatostatin receptor 2controlled releaseesterase responsivetumor targeting

Identifiers

PMID27284243
PMCPMC4883818
OpenAlexW2404909905

What OpenQuestion holds

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LicenceCC BY-NC
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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.