Evidence map›Paper›PMID 31194786›Full record

ArticlePloS one2019

Targeting DNA-dependent protein kinase sensitizes hepatocellular carcinoma cells to proton beam irradiation through apoptosis induction.

Changhoon Choi, Arang Son, Ga-Haeng Lee, Sung-Won Shin, Sohee Park, Sang Hee Ahn, Yoonsun Chung, Jeong Il Yu, Hee Chul Park

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 17 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

9 authors at 3 institutions in 1 country.

Changhoon ChoiDepartment of Radiation Oncology, Samsung Medical Center, Seoul, South Korea.
Arang SonDepartment of Radiation Oncology, Samsung Medical Center, Seoul, South Korea.
Ga-Haeng LeeDepartment of Radiation Oncology, Samsung Medical Center, Seoul, South Korea.
Sung-Won ShinDepartment of Radiation Oncology, Samsung Medical Center, Seoul, South Korea.
Sohee ParkDepartment of Radiation Oncology, Samsung Medical Center, Seoul, South Korea.
Sang Hee AhnSungkyunkwan University School of Medicine, Seoul, South Korea.
Yoonsun ChungDepartment of Nuclear Engineering, Hanyang University, Seoul, South Korea.
Jeong Il YuDepartment of Radiation Oncology, Samsung Medical Center, Seoul, South Korea.
Hee Chul ParkDepartment of Radiation Oncology, Samsung Medical Center, Seoul, South Korea.ORCID 0000-0003-0385-9681
Samsung Medical Center · KRHanyang University · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have highlighted the implications of genetic variations in the relative biological effectiveness (RBE) of proton beam irradiation over conventional X-ray irradiation. Proton beam radiotherapy is a reasonable radiotherapy option for hepatocellular carcinoma (HCC), but the impact of genetic difference on the HCC RBE remains unknown. Here, we determined proton RBE in human HCC cells by exposing them to various doses of either 6-MV X-rays or 230-MeV proton beams. Clonogenic survival assay revealed variable radiosensitivity of human HCC cell lines with survival fraction at 2 Gy ranging from 0.38 to 0.83 and variable proton RBEs with 37% survival fraction ranging from 1.00 to 1.48. HCC cells appeared more sensitive to proton irradiation than X-rays, with more persistent activation of DNA damage repair proteins over time. Depletion of a DNA damage repair gene, DNA-PKcs, by siRNA dramatically increased the sensitivity of HCC cells to proton beams with a decrease in colony survival and an increase in apoptosis. Our findings suggest that there are large variations in proton RBE in HCC cells despite the use of a constant RBE of 1.1 in the clinic and targeting DNA-PKcs in combination with proton beam therapy may be a promising regimen for treating HCC.

Indexed as

ApoptosisCarcinoma, HepatocellularCell DeathCell Line, TumorCell SurvivalDNA-Activated Protein KinaseDNA DamageDNA RepairDose-Response Relationship, RadiationHumansLiver NeoplasmsProton TherapyRadiation ToleranceRelative Biological EffectivenessTreatment OutcomeDNA-Activated Protein Kinase

Identifiers

PMID31194786
PMCPMC6563991
OpenAlexW2953197092

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.