Evidence map›Paper›PMID 22496834›Full record

ArticlePloS one2012

Recombinant human endostatin normalizes tumor vasculature and enhances radiation response in xenografted human nasopharyngeal carcinoma models.

Fang Peng, Zumin Xu, Jin Wang, Yuanyuan Chen, Qiang Li, Yufang Zuo, Jing Chen, Xiao Hu, Qichao Zhou, Yan Wang and 3 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.0field-weighted citation impact, top 8% 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.

NCT02590133 phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Multi-institutional, Randomized Controlled, Phase II Clinical Trial on Comparison of Efficacy and Safety of Nedaplatin Plus 5-Fu Combined With and Without Endostar® Continuous Intravenous Infusion in Refractory Nasopharyngeal Carcinoma

TypeinterventionalSponsorYun-fei XiaRan2015 to 2020Enrolled328ConditionsNasopharyngeal CarcinomaArmsRecombinant Human Endostatin Injection (Endostar), Fluorouracil (5-Fu), Nedaplatin
NCT02636231 phase2unknown statusnot on this mapstarted 2015, after this paper: background citation

A Phase II Randomized Controlled Study to Compare Endostar and IMRT vs. IMRT Alone for Locally Recurrent Nasopharyngeal Carcinoma Patients

TypeinterventionalSponsorSun Yat-sen UniversityRan2015 to 2021Enrolled96ConditionsNasopharyngeal CarcinomaArmsEndostatins, IMRT
3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 67 citations in OpenAlex.

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  12. Modulation of vascular response after injury in the rat Achilles tendon alters healing capacity.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2021
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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

13 authors at 3 institutions in 1 country.

Fang PengDepartment of Radiation Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong Province, China.
Zumin Xu
Jin Wang
Yuanyuan Chen
Qiang Li
Yufang Zuo
Jing Chen
Xiao Hu
Qichao Zhou
Yan Wang
Honglian Ma
Yong Bao
Ming Chen
Sun Yat-sen University · CNGeneral Hospital of Guangzhou Military Command · CNGuangdong Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHypoxic tumor cells can reduce the efficacy of radiation. Antiangiogenic therapy may transiently "normalize" the tumor vasculature to make it more efficient for oxygen delivery. The aim of this study is to investigate whether the recombinant human endostatin (endostar) can create a "vascular normalization window" to alleviate hypoxia and enhance the inhibitory effects of radiation therapy in human nasopharyngeal carcinoma (NPC) in mice. METHODOLOGY/PRINCIPAL

findingsTransient changes in morphology of tumor vasculature and hypoxic tumor cell fraction in response to endostar were detected in mice bearing CNE-2 and 5-8F human NPC xenografts. Various treatment schedules were tested to assess the influence of endostar on the effect of radiation therapy. Several important factors relevant to the angiogenesis were identified through immunohistochemical staining. During endostar treatment, tumor vascularity decreased, while the basement membrane and pericyte coverage associated with endothelial cells increased, which supported the idea of vessel normalization. Hypoxic tumor cell fraction also decreased after the treatment. The transient modulation of tumor physiology caused by endostar improved the effect of radiation treatment compared with other treatment schedules. The expressions of vascular endothelial growth factor (VEGF), matrix metalloproteinase-2 (MMP-2), MMP-9, and MMP-14 decreased, while the level of pigment epithelium-derived factor (PEDF) increased.

conclusionsEndostar normalized tumor vasculature, which alleviated hypoxia and significantly sensitized the function of radiation in anti-tumor in human NPC. The results provide an important experimental basis for combining endostar with radiation therapy in human NPC.

Indexed as

Radiation ToleranceAngiogenesis InhibitorsAnimalsBasement MembraneCarcinomaCell Line, TumorEndostatinsEye ProteinsHumansImmunohistochemistryMaleMatrix Metalloproteinase 14Matrix Metalloproteinase 2MiceMice, NudeNasopharyngeal CarcinomaAngiogenesis Inhibitorsendostar proteinEndostatinsEye ProteinsMatrix Metalloproteinase 14Matrix Metalloproteinase 2MMP14 protein, humanMMP2 protein, humanNerve Growth FactorsPigment Epithelium-Derived FactorRecombinant ProteinsSerpinsVascular Endothelial Growth Factor A

Identifiers

PMID22496834
PMCPMC3322143
OpenAlexW2082979902

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.