Evidence map›Paper›PMID 25284063›Full record

ArticleRadiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology2014

Determinates of tumor response to radiation: tumor cells, tumor stroma and permanent local control.

Wende Li, Peigen Huang, David J Chen, Leo E Gerweck

Abstract read
In one paragraph

Article in Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
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

4 authors at 2 institutions in 2 countries.

Wende LiDepartment of Radiation Oncology, Massachusetts General Hospital, Boston, USA; Guangdong Medical College, PR China.
Peigen HuangDepartment of Radiation Oncology, Massachusetts General Hospital, Boston, USA.
David J ChenDepartment of Radiation Oncology, University of Texas Southwestern Medical Center, Dallas, USA.
Leo E GerweckDepartment of Radiation Oncology, Massachusetts General Hospital, Boston, USA. Electronic address: LGerweck@mgh.harvard.edu.
Massachusetts General Hospital · USThe University of Texas Southwestern Medical Center · US

Funding

PROTON THERAPY RESEARCH AND TREATMENT CENTERC06CA059267 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI GOITEIN, MICHAEL · 1992 to 1995
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NCI NIH HHS C06 CA059267
6 · The paper itself

Abstract

background and purposeThe causes of tumor response variation to radiation remain obscure, thus hampering the development of predictive assays and strategies to decrease resistance. The present study evaluates the impact of host tumor stromal elements and the in vivo environment on tumor cell kill, and relationship between tumor cell radiosensitivity and the tumor control dose. MATERIAL AND

methodsFive endpoints were evaluated and compared in a radiosensitive DNA double-strand break repair-defective (DNA-PKcs(-/-)) tumor line, and its DNA-PKcs repair competent transfected counterpart. In vitro colony formation assays were performed on in vitro cultured cells, on cells obtained directly from tumors, and on cells irradiated in situ. Permanent local control was assessed by the TCD50 assay. Vascular effects were evaluated by functional vascular density assays.

resultsThe fraction of repair competent and repair deficient tumor cells surviving radiation did not substantially differ whether irradiated in vitro, i.e., in the absence of host stromal elements and factors, from the fraction of cells killed following in vivo irradiation. Additionally, the altered tumor cell sensitivity resulted in a proportional change in the dose required to achieve permanent local control. The estimated number of tumor cells per tumor, their cloning efficiency and radiosensitivity, all assessed by in vitro assays, were used to predict successfully, the measured tumor control doses.

conclusionThe number of clonogens per tumor and their radiosensitivity govern the permanent local control dose.

Indexed as

AnimalsApoptosisCell Line, TumorDNA-Activated Protein KinaseDNA Breaks, Double-StrandedLethal Dose 50Mice, NudeMice, SCIDNeoplasmsNeoplasm TransplantationRadiation ToleranceRadiotherapy DosageStromal CellsTransfectionTumor Cells, CulturedDNA-Activated Protein KinaseIntrinsic radiosensitivityPredictive assaysRadiationTumor control doseTumor vasculature

Identifiers

PMID25284063
PMCPMC4280081
OpenAlexW2119327949

What OpenQuestion holds

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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.