Evidence map›Paper›PMID 27659522›Full record

ArticleOncotarget2016

Multi-cycle chemotherapy with the glycolipid-like polymeric micelles evade cancer stem cell enrichment in breast cancer therapy.

Tingting Meng, Jingwen Liu, Lijuan Wen, Ming Yuan, Bolin Cheng, Yingwen Hu, Yun Zhu, Xuan Liu, Hong Yuan, Fuqiang Hu

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Tingting MengInstitute of Pharmaceutics, College of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, China.
Jingwen LiuInstitute of Pharmaceutics, College of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, China.
Lijuan WenInstitute of Pharmaceutics, College of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, China.
Ming YuanInstitute of Pharmaceutics, College of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, China.
Bolin ChengInstitute of Pharmaceutics, College of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, China.
Yingwen HuInstitute of Pharmaceutics, College of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, China.
Yun ZhuInstitute of Pharmaceutics, College of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, China.
Xuan LiuInstitute of Pharmaceutics, College of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, China.
Hong YuanInstitute of Pharmaceutics, College of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, China.
Fuqiang HuInstitute of Pharmaceutics, College of Pharmaceutical Science, Zhejiang University, Hangzhou 310058, China.
Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multi-cycle chemotherapy is commonly used in the clinic, while the phenomena of enrichment of cancer stem cells (CSCs) and enhanced multi-drug resistance (MDR) are commonly involved. This research was designed for evaluating this successive administration. Chitosan oligosaccharide-g-stearic acid (CSOSA) polymer was used as the drug delivery system (DDS) to perform tri-cycle chemotherapy on a new tumor model induced by mammosphere cells. In vitro, on CSCs enriched mammospheres model, the doxorubicin-loaded CSOSA (CSOSA/DOX) displayed an improved growth inhibition effect measured by acid phosphatase assay (APH). While in vivo, the CSOSA/DOX micelles blocked tumor progression and led to a marked decrease of CSCs proportion as well as MDR capacity. What's more, the CSOSA/DOX helped decay the microenvironment and attenuate systemic side effects. We concluded that the CSOSA polymer could be a potential DDS for long-term multi-cycle chemotherapy in antitumor research.

Indexed as

GlycolipidsMicellesPolymersAnimalsAntineoplastic AgentsBreast NeoplasmsCell Line, TumorChitosanDisease Models, AnimalDoxorubicinFemaleHumansMiceNeoplastic Stem CellsSpheroids, CellularTreatment OutcomeAntineoplastic AgentsChitosanDoxorubicinGlycolipidsMicellesPolymerscancer stem celldrug deliverymicroenvironmentmulti-cycle chemotherapytumor repopulation

Identifiers

PMID27659522
PMCPMC5341957
OpenAlexW2523603169

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.