An ionising radiation-induced specific transcriptional signature of inflammation-associated genes in whole blood from radiotherapy patients: a pilot study

被引:5
|
作者
Cruz-Garcia, Lourdes [1 ]
Badie, Christophe [1 ,4 ]
Anbalagan, Selvakumar [2 ,3 ]
Moquet, Jayne [1 ]
Gothard, Lone [2 ,3 ]
O'Brien, Grainne [1 ]
Somaiah, Navita [2 ,3 ]
Ainsbury, Elizabeth A. [1 ,4 ]
机构
[1] PHE CRCE, Oxford OX11 0RQ, England
[2] Inst Canc Res, London SM2 5NG, England
[3] Royal Marsden NHS Fdn Trust, London SM2 5NG, England
[4] Imperial Coll Sci Technol & Med, Sch Publ Hlth, Fac Med, Environm Res Grp, London, England
关键词
Ionising radiation; Blood; Gene expression; Transcription; NCounter; RT-qPCR; Inflammation; Radiotherapy; Cancer; IN-VIVO; EXPRESSION; EXPOSURE; RENEB; INTERLEUKIN-18; BIOMARKER; THERAPY; INNATE; CELLS;
D O I
10.1186/s13014-021-01807-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background This communication reports the identification of a new panel of transcriptional changes in inflammation-associated genes observed in response to ionising radiation received by radiotherapy patients. Methods Peripheral blood samples were taken with ethical approval and informed consent from a total of 20 patients undergoing external beam radiotherapy for breast, lung, gastrointestinal or genitourinary tumours. Nanostring nCounter analysis of transcriptional changes was carried out in samples prior and 24 h post-delivery of the 1st radiotherapy fraction, just prior to the 5th or 6th fraction, and just before the last fraction. Results Statistical analysis with BRB-ArrayTools, GLM MANOVA and nSolver, revealed a radiation responsive panel of genes which varied by patient group (type of cancer) and with time since exposure (as an analogue for dose received), which may be useful as a biomarker of radiation response. Conclusion Further validation in a wider group of patients is ongoing, together with work towards a full understanding of patient specific responses in support of personalised approaches to radiation medicine.
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页数:10
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