Evidence map›Paper›PMID 24742865›Full record

ArticleTranslational oncology2014

Antiangiogenic therapy using sunitinib combined with rapamycin retards tumor growth but promotes metastasis.

Tao Yin, Sisi He, Tinghong Ye, Guobo Shen, Yang Wan, Yongsheng Wang

Open access · goldAbstract read
In one paragraph

Article in Translational oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

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  12. Targeting metastasis.Nature reviews. Cancer · 2016
    Review
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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

6 authors at 2 institutions in 1 country.

Tao YinState Key Laboratory of Biotherapy, West China School of Medicine, West China Hospital, Sichuan University, Chengdu, People's Republic of China. Electronic address: yintao03073@163.com.
Sisi HeState Key Laboratory of Biotherapy, West China School of Medicine, West China Hospital, Sichuan University, Chengdu, People's Republic of China. Electronic address: chrinstina-hesisi@yahoo.cn.
Tinghong YeState Key Laboratory of Biotherapy, West China School of Medicine, West China Hospital, Sichuan University, Chengdu, People's Republic of China. Electronic address: yetinghong0908@163.com.
Guobo ShenState Key Laboratory of Biotherapy, West China School of Medicine, West China Hospital, Sichuan University, Chengdu, People's Republic of China. Electronic address: shengguobo@126.com.
Yang WanState Key Laboratory of Biotherapy, West China School of Medicine, West China Hospital, Sichuan University, Chengdu, People's Republic of China. Electronic address: wanyang1110@gmail.com.
Yongsheng WangState Key Laboratory of Biotherapy, West China School of Medicine, West China Hospital, Sichuan University, Chengdu, People's Republic of China; Department of Thoracic Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, People's Republic of China. Electronic address: wangys75@gmail.com.
Sichuan University · CNState Key Laboratory of Biotherapy

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study investigated the synergistic effect of sunitinib and rapamycin on tumor growth and metastasis in murine breast cancer model.

methodsThe synergistic antitumor effect of sunitinib and rapamycin on tumor growth and metastasis was investigated. Myeloid-derived suppressor cells (MDSCs) in spleens and lungs were assessed. Tumor hypoxia, vessel density and micrometastasis were evaluated. Versican, indoleamine 2,3-dioxygenase (IDO), arginase 1, interleukin-6 (IL-6), IL-10, and transforming growth factor β (TGF-β) in the lungs and tumors were examined. IL-6 and TGF-β in the blood were evaluated.

resultsSynergism between sunitinib and rapamycin on tumor growth was observed. Sunitinib plus rapamycin reduced splenomegaly, MDSCs in spleens and lungs, and microvessel density in tumor microenvironment, while exacerbated hypoxia and promoted cancer lung metastasis. Sunitinib plus rapamycin markedly induced versican, IDO, arginase 1, IL-6, and TGF-β expression in the lungs, whereas it reduced IDO and IL-10 expression in the primary tumor tissues. IL-6 levels in the circulation were increased after rapamycin and combination therapies.

conclusionsThe combination of sunitinib plus rapamycin reduced the tumor growth but promoted tumor metastasis. This study warrants that further mTOR inhibition treatment should be closely watched in clinical setting, especially combined with antiangiogenic therapy.

Identifiers

PMID24742865
PMCPMC4101341
OpenAlexW2088516219

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.