Evidence map›Paper›PMID 24510029›Full record

ArticleBlood cancer journal2014

A novel strategy inducing autophagic cell death in Burkitt's lymphoma cells with anti-CD19-targeted liposomal rapamycin.

K Ono, T Sato, S Iyama, A Tatekoshi, A Hashimoto, Y Kamihara, H Horiguchi, S Kikuchi, Y Kawano, K Takada and 6 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.4field-weighted citation impact, top 35% 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

7 citing papers in PubMed, 12 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

16 authors at 1 institution in 1 country.

K OnoDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
T SatoDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
S IyamaDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
A TatekoshiDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
A HashimotoDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Y KamiharaDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
H HoriguchiDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
S KikuchiDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Y KawanoDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
K TakadaDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
T HayashiDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
K MiyanishiDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Y SatoDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
R TakimotoDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
M KobuneDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
J KatoDepartment of Medical Oncology and Hematology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Sapporo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Relapsed or refractory Burkitt's lymphoma often has a poor prognosis in spite of intensive chemotherapy that induces apoptotic and/or necrotic death of lymphoma cells. Rapamycin (Rap) brings about autophagy, and could be another treatment. Further, anti-CD19-targeted liposomal delivery may enable Rap to kill lymphoma cells specifically. Rap was encapsulated by anionic liposome and conjugated with anti-CD19 antibody (CD19-GL-Rap) or anti-CD2 antibody (CD2-GL-Rap) as a control. A fluorescent probe Cy5.5 was also liposomized in the same way (CD19 or CD2-GL-Cy5.5) to examine the efficacy of anti-CD19-targeted liposomal delivery into CD19-positive Burkitt's lymphoma cell line, SKW6.4. CD19-GL-Cy5.5 was more effectively uptaken into SKW6.4 cells than CD2-GL-Cy5.5 in vitro. When the cells were inoculated subcutaneously into nonobese diabetic/severe combined immunodeficiency mice, intravenously administered CD19-GL-Cy5.5 made the subcutaneous tumor fluorescent, while CD2-GL-Cy5.5 did not. Further, CD19-GL-Rap had a greater cytocidal effect on not only SKW6.4 cells but also Burkitt's lymphoma cells derived from patients than CD2-GL-Rap in vitro. The specific toxicity of CD19-GL-Rap was cancelled by neutralizing anti-CD19 antibody. The survival period of mice treated with intravenous CD19-GL-Rap was significantly longer than that of mice treated with CD2-GL-Rap after intraperitoneal inoculation of SKW6.4 cells. Anti-CD19-targeted liposomal Rap could be a promising lymphoma cell-specific treatment inducing autophagic cell death.

Identifiers

PMID24510029
PMCPMC3944660
OpenAlexW2034261032

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.