Evidence map›Paper›PMID 26436767›Full record

ArticleCancer biology & therapy2015

Interleukin-4 receptor-targeted liposomal doxorubicin as a model for enhancing cellular uptake and antitumor efficacy in murine colorectal cancer.

Chih-Yung Yang, Hong-Wen Liu, Ya-Ching Tsai, Ju-Yu Tseng, Shu-Ching Liang, Chin-Yau Chen, Wei-Nan Lian, Ming-Cheng Wei, Maggie Lu, Ruey-Hwa Lu and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2015. 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
0.8field-weighted citation impact, top 29% 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, 23 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

12 authors at 5 institutions in 3 countries.

Chih-Yung Yanga Department of Education and Research ; Taipei City Hospital ; Taipei , Taiwan.
Hong-Wen Liub Institute of Microbiology and Immunology, National Yang-Ming University ; Taipei , Taiwan.
Ya-Ching Tsaib Institute of Microbiology and Immunology, National Yang-Ming University ; Taipei , Taiwan.
Ju-Yu Tsengb Institute of Microbiology and Immunology, National Yang-Ming University ; Taipei , Taiwan.
Shu-Ching Liangb Institute of Microbiology and Immunology, National Yang-Ming University ; Taipei , Taiwan.
Chin-Yau Chenc Department of Surgery ; National Yang-Ming University Hospital ; Yilan , Taiwan.
Wei-Nan Lianb Institute of Microbiology and Immunology, National Yang-Ming University ; Taipei , Taiwan.
Ming-Cheng Weid Drug Delivery Lab, Biomedical Technology and Device Research Laboratories, Industrial Technology Research Institute ; HsinChu , Taiwan.
Maggie Lud Drug Delivery Lab, Biomedical Technology and Device Research Laboratories, Industrial Technology Research Institute ; HsinChu , Taiwan.
Ruey-Hwa Lue Department of Surgery ; Taipei City Hospital ; Taipei , Taiwan.
Chi-Hung Lina Department of Education and Research ; Taipei City Hospital ; Taipei , Taiwan.
Jeng-Kai Jiangf School of Medicine, National Yang-Ming University ; Taipei , Taiwan.
National Yang Ming Chiao Tung University · TWCzech Academy of Sciences, Institute of Microbiology · CZITRI International · USTaipei City Hospital · TWTaipei Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our previous studies showed that colorectal tumor has high interleukin-4 receptor α (IL-4Rα) expression, whereas adjacent normal tissue has low or no IL-4Rα expression. We also observed that human atherosclerotic plaque-specific peptide-1 (AP1) can specifically target to IL-4Rα. In this study, we investigated the therapeutic efficacy and systemic toxicity of AP1-conjuagted liposomal doxorubicin. AP1 bound more strongly to and was more efficiently internalized into IL-4Rα-overexpressing CT26 cells than CT26 control cells. Selective cytotoxicity experiment revealed that AP1-conjugated liposomal doxorubicin preferentially killed IL-4Rα-overexpressing CT26 cells. AP1-conjugated liposomal doxorubicin administered intravenously into mice produced significant inhibition of tumor growth and showed decreased cardiotoxicity of doxorubicin. These results indicated that AP1-conjugated liposomal doxorubicin has a potent and selective anticancer potential against IL-4Rα-overexpressing colorectal cancer cells, thus providing a model for targeted anticancer therapy.

Indexed as

AnimalsAntibiotics, AntineoplasticApoptosisCell Line, TumorColorectal NeoplasmsDoxorubicinDrug Screening Assays, AntitumorHumansLiposomesMaleMiceMice, Inbred BALB CNeoplasm TransplantationPeptidesReceptors, Interleukin-4Treatment OutcomeAntibiotics, AntineoplasticAP1 peptideDoxorubicinLiposomesPeptidesReceptors, Interleukin-4AP1colorectal cancerinterleukin-4 receptor αtargeted drug delivery

Identifiers

PMID26436767
PMCPMC4846110
OpenAlexW2173005431

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.