Evidence map›Paper›PMID 27119104›Full record

ArticleMolecular therapy oncolytics2015

L-Asparaginase delivered by Salmonella typhimurium suppresses solid tumors.

Kwangsoo Kim, Jae Ho Jeong, Daejin Lim, Yeongjin Hong, Hyung-Ju Lim, Geun-Joong Kim, So-Ra Shin, Je-Jung Lee, Misun Yun, Robert A Harris and 2 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy oncolytics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

25 citing papers in PubMed, 52 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 3 institutions in 2 countries.

Kwangsoo KimDepartment of Microbiology, Chonnam National University Medical School, Gwangju, Republic of Korea; Department of Molecular Medicine, Chonnam National University Graduate School, Gwangju, Republic of Korea.
Jae Ho JeongDepartment of Microbiology, Chonnam National University Medical School, Gwangju, Republic of Korea; Department of Molecular Medicine, Chonnam National University Graduate School, Gwangju, Republic of Korea.
Daejin LimDepartment of Microbiology, Chonnam National University Medical School, Gwangju, Republic of Korea; Department of Molecular Medicine, Chonnam National University Graduate School, Gwangju, Republic of Korea.
Yeongjin HongDepartment of Microbiology, Chonnam National University Medical School, Gwangju, Republic of Korea; Department of Molecular Medicine, Chonnam National University Graduate School, Gwangju, Republic of Korea.
Hyung-Ju LimDepartment of Microbiology, Chonnam National University Medical School, Gwangju, Republic of Korea; Department of Molecular Medicine, Chonnam National University Graduate School, Gwangju, Republic of Korea.
Geun-Joong KimDepartment of Biological Sciences, College of Natural Sciences, Chonnam National University , Gwangju, Korea.
So-Ra ShinDepartment of Biological Sciences, College of Natural Sciences, Chonnam National University , Gwangju, Korea.
Je-Jung LeeDepartment of Molecular Medicine, Chonnam National University Graduate School, Gwangju, Republic of Korea; Department of Hematology-Oncology, Chonnam National University Hwasun Hospital, Jeollanamdo, Republic of Korea.
Misun YunDepartment of Molecular Medicine, Chonnam National University Graduate School, Gwangju, Republic of Korea; Department of Nuclear Medicine, Chonnam National University Hwasun Hospital, Jeollanamdo, Republic of Korea.
Robert A HarrisRoudebush VA Medical Center and the Department of Biochemistry and Molecular Biology, Indiana University School of Medicine , Indianapolis, Indiana, USA.
Jung-Joon MinDepartment of Molecular Medicine, Chonnam National University Graduate School, Gwangju, Republic of Korea; Department of Nuclear Medicine, Chonnam National University Hwasun Hospital, Jeollanamdo, Republic of Korea.
Hyon E ChoyDepartment of Microbiology, Chonnam National University Medical School, Gwangju, Republic of Korea; Department of Molecular Medicine, Chonnam National University Graduate School, Gwangju, Republic of Korea.
Chonnam National University · KRChonnam National University Hospital · KRIndiana University – Purdue University Indianapolis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bacteria can be engineered to deliver anticancer proteins to tumors via a controlled expression system that maximizes the concentration of the therapeutic agent in the tumor. L-asparaginase (L-ASNase), which primarily converts asparagine to aspartate, is an anticancer protein used to treat acute lymphoblastic leukemia. In this study, Salmonellae were engineered to express L-ASNase selectively within tumor tissues using the inducible araBAD promoter system of Escherichia coli. Antitumor efficacy of the engineered bacteria was demonstrated in vivo in solid malignancies. This result demonstrates the merit of bacteria as cancer drug delivery vehicles to administer cancer-starving proteins such as L-ASNase to be effective selectively within the microenvironment of cancer tissue.

Identifiers

PMID27119104
PMCPMC4845971
OpenAlexW2471497744

What OpenQuestion holds

Textmetadata
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.