Evidence map›Paper›PMID 30804471›Full record

ArticleCell death and differentiation2019

Ly6G

Hee-Young Jeon, Seok Won Ham, Jun-Kyum Kim, Xiong Jin, Seon Yong Lee, Yong Jae Shin, Chang-Yong Choi, Jason K Sa, Se Hoon Kim, Taehoon Chun and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

27 citing papers in PubMed, 42 citations in OpenAlex.

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  17. Glioblastoma - treatment and obstacles.Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2022
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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 3 countries.

Hee-Young JeonDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea.
Seok Won HamDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea.
Jun-Kyum KimDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea.
Xiong JinDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea.
Seon Yong LeeDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea.
Yong Jae ShinDepartment of Neurosurgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Chang-Yong ChoiDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea.
Jason K SaInstitute for Refractory Cancer Research, Research Institute for Future Medicine, Samsung Medical Center, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-3251-5004
Se Hoon KimDepartment of Pathology, College of Medicine, Yonsei University, Seoul, Republic of Korea.
Taehoon ChunDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea.
Xun JinTianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Do-Hyun NamDepartment of Neurosurgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Hyunggee KimDepartment of Biotechnology, College of Life Sciences and Biotechnology, Korea University, Seoul, Republic of Korea. hg-kim@korea.ac.kr.
Korea University · KRSamsung Medical Center · KRYonsei University · KR

Funding

Korea Health Industry Development Institute (KHIDI) HI14C3418National Natural Science Foundation of China (National Science Foundation of China) 81572891National Research Foundation of Korea (NRF) 2013M2A2A7042530National Research Foundation of Korea (NRF) 2016M3C7A1913844
6 · The paper itself

Abstract

Most glioblastomas frequently recur at sites of radiotherapy, but it is unclear if changes in the tumor microenvironment due to radiotherapy influence glioblastoma recurrence. Here, we demonstrate that radiation-induced senescent glioblastoma cells exhibit a senescence-associated secretory phenotype that functions through NFκB signaling to influence changes in the tumor microenvironment, such as recruitment of Ly6G

Indexed as

AnimalsAntigens, LyBrain NeoplasmsCell Line, TumorGlioblastomaHumansMiceMice, NudeNeoplastic Stem CellsTransfectionAntigens, LyLy6G antigen, mouse

Identifiers

PMID30804471
PMCPMC6748155
OpenAlexW2915918807

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.