Evidence map›Paper›PMID 26023798›Full record

ArticleOncotarget2015

A combination of YM-155, a small molecule survivin inhibitor, and IL-2 potently suppresses renal cell carcinoma in murine model.

Kai Guo, Peng Huang, Naijin Xu, Peng Xu, Haruki Kaku, Shaobo Zheng, Abai Xu, Eiji Matsuura, Chunxiao Liu, Hiromi Kumon

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 22 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 4 institutions in 2 countries.

Kai GuoDepartment of Urology, Zhujiang Hospital, Southern Medical University, Guangzhou, People's Republic of China.
Peng HuangDepartment of Urology, Zhujiang Hospital, Southern Medical University, Guangzhou, People's Republic of China.
Naijin XuDepartment of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Peng XuDepartment of Urology, Zhujiang Hospital, Southern Medical University, Guangzhou, People's Republic of China.
Haruki KakuDepartment of Urology, Okamura Isshindow Hospital, Okayama, Japan.
Shaobo ZhengDepartment of Urology, Zhujiang Hospital, Southern Medical University, Guangzhou, People's Republic of China.
Abai XuDepartment of Urology, Zhujiang Hospital, Southern Medical University, Guangzhou, People's Republic of China.
Eiji MatsuuraOkayama Medical Innovation Center, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Chunxiao LiuDepartment of Urology, Zhujiang Hospital, Southern Medical University, Guangzhou, People's Republic of China.
Hiromi KumonDepartment of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Southern Medical University · CNOkayama University · JPOkayama University Hospital · JPZhujiang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

YM155, a small molecule inhibitor of the antiapoptotic protein survivin, has been developed as a potential anti-cancer drug. We investigated a combination therapy of YM155 and interleukin-2 (IL-2) in a mouse model of renal cell carcinoma (RCC). YM155 caused cell cycle arrest and apoptosis in renal cancer (RENCA) cells. Next, luciferase-expressing RENCA cells were implanted in the left kidney and the lung of BALB/c mice to develop RCC metastatic model. In this orthotopic renal and metastatic lung tumors models, YM155 and IL-2 additively decreased tumor weight, lung metastasis, and luciferin-stained tumor images. Also, the combination significantly suppressed regulatory T cells and myeloid-derived suppressor cells compared with single agent treatment. We suggest that a combination of YM155 and IL-2 can be tested as a potential therapeutic modality in patients with RCC.

Indexed as

AnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Renal CellCD4-Positive T-LymphocytesCell Line, TumorCell ProliferationCell SeparationDisease Models, AnimalFemaleFlow CytometryGene Expression Regulation, NeoplasticHumansImidazolesInhibitor of Apoptosis ProteinsInterleukin-2Antineoplastic AgentsBIRC5 protein, humanImidazolesInhibitor of Apoptosis ProteinsInterleukin-2NaphthoquinonessepantroniumSurvivininterleukin-2IVISMDSCsrenal cell carcinomaTregYM155

Identifiers

PMID26023798
PMCPMC4673255
OpenAlexW1598614727

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.