Evidence map›Paper›PMID 25925410›Full record

ArticleBMC cancer2015

Transient elevation of glycolysis confers radio-resistance by facilitating DNA repair in cells.

Anant Narayan Bhatt, Ankit Chauhan, Suchit Khanna, Yogesh Rai, Saurabh Singh, Ravi Soni, Namita Kalra, Bilikere S Dwarakanath

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 5% 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

65 citing papers in PubMed, 1 synthesis or guideline pooled it, 115 citations in OpenAlex.

  1. Pooled it
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  11. Resistance to Radiotherapy in Cancer.Diseases (Basel, Switzerland) · 2025
    Review
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5 more citing papers are in PubMed but not listed here.

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

8 authors at 1 institution in 1 country.

Anant Narayan BhattMetabolic and Cell Signaling Group, Institute of Nuclear Medicine and Allied Sciences, Brig SK Mazumdar Road, New Delhi, Delhi, 110 054, India. anant@inmas.drdo.in.
Ankit ChauhanMetabolic and Cell Signaling Group, Institute of Nuclear Medicine and Allied Sciences, Brig SK Mazumdar Road, New Delhi, Delhi, 110 054, India. ankitvkc@gmail.com.
Suchit KhannaMetabolic and Cell Signaling Group, Institute of Nuclear Medicine and Allied Sciences, Brig SK Mazumdar Road, New Delhi, Delhi, 110 054, India. suchit.khanna1985@gmail.com.
Yogesh RaiMetabolic and Cell Signaling Group, Institute of Nuclear Medicine and Allied Sciences, Brig SK Mazumdar Road, New Delhi, Delhi, 110 054, India. mahadev.kashi@gmail.com.
Saurabh SinghMetabolic and Cell Signaling Group, Institute of Nuclear Medicine and Allied Sciences, Brig SK Mazumdar Road, New Delhi, Delhi, 110 054, India. saurabh_11may@yahoo.co.in.
Ravi SoniMetabolic and Cell Signaling Group, Institute of Nuclear Medicine and Allied Sciences, Brig SK Mazumdar Road, New Delhi, Delhi, 110 054, India. soniravi09@rediffmail.com.
Namita KalraMetabolic and Cell Signaling Group, Institute of Nuclear Medicine and Allied Sciences, Brig SK Mazumdar Road, New Delhi, Delhi, 110 054, India. namitaji@rediffmail.com.
Bilikere S DwarakanathMetabolic and Cell Signaling Group, Institute of Nuclear Medicine and Allied Sciences, Brig SK Mazumdar Road, New Delhi, Delhi, 110 054, India. dwarakanathdrbs@gmail.com.
Institute of Nuclear Medicine & Allied Sciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCancer cells exhibit increased glycolysis for ATP production (the Warburg effect) and macromolecular biosynthesis; it is also linked with therapeutic resistance that is generally associated with compromised respiratory metabolism. Molecular mechanisms underlying radio-resistance linked to elevated glycolysis remain incompletely understood.

methodsWe stimulated glycolysis using mitochondrial respiratory modifiers (MRMs viz. di-nitro phenol, DNP; Photosan-3, PS3; Methylene blue, MB) in established human cell lines (HEK293, BMG-1 and OCT-1). Glucose utilization and lactate production, levels of glucose transporters and glycolytic enzymes were investigated as indices of glycolysis. Clonogenic survival, DNA repair and cytogenetic damage were studied as parameters of radiation response.

resultsMRMs induced the glycolysis by enhancing the levels of two important regulators of glucose metabolism GLUT-1 and HK-II and resulted in 2 fold increase in glucose consumption and lactate production. This increase in glycolysis resulted in resistance against radiation-induced cell death (clonogenic survival) in different cell lines at an absorbed dose of 5 Gy. Inhibition of glucose uptake and glycolysis (using fasentin, 2-deoxy-D-glucose and 3-bromopyruvate) in DNP treated cells failed to increase the clonogenic survival of irradiated cells, suggesting that radio-resistance linked to inhibition of mitochondrial respiration is glycolysis dependent. Elevated glycolysis also facilitated rejoining of radiation-induced DNA strand breaks by activating both non-homologous end joining (NHEJ) and homologous recombination (HR) pathways of DNA double strand break repair leading to a reduction in radiation-induced cytogenetic damage (micronuclei formation) in these cells.

conclusionsThese findings suggest that enhanced glycolysis generally observed in cancer cells may be responsible for the radio-resistance, partly by enhancing the repair of DNA damage.

Indexed as

Radiation ToleranceCell RespirationCell SurvivalDinitrophenolsDNA DamageDNA RepairDNA Repair EnzymesGlycolysisHEK293 CellsHumansMitochondriaDinitrophenolsDNA Repair Enzymes

Identifiers

PMID25925410
PMCPMC4425929
OpenAlexW2057909622

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.