Raman spectroscopy identifies radiation response in human non-small cell lung cancer xenografts

被引:0
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作者
Samantha J. Harder
Martin Isabelle
Lindsay DeVorkin
Julian Smazynski
Wayne Beckham
Alexandre G. Brolo
Julian J. Lum
Andrew Jirasek
机构
[1] University of Victoria,Department of Physics and Astronomy
[2] PO Box 1700 STN CSC,Department of Chemistry
[3] Victoria,Department of Biochemistry and Microbiology
[4] British Columbia,undefined
[5] V8W 2Y2,undefined
[6] Canada,undefined
[7] BC Cancer Agency—Vancouver Island Centre,undefined
[8] Trev and Joyce Deeley Research Centre,undefined
[9] 2410 Lee Ave.,undefined
[10] Victoria,undefined
[11] British Columbia,undefined
[12] V8R 6V5,undefined
[13] Canada ,undefined
[14] BC Cancer Agency—Vancouver Island Centre,undefined
[15] Medical Physics,undefined
[16] 2410 Lee Ave.,undefined
[17] Victoria,undefined
[18] British Columbia,undefined
[19] V8R 6V5,undefined
[20] Canada ,undefined
[21] University of Victoria,undefined
[22] PO Box 3065,undefined
[23] Victoria,undefined
[24] British Columbia,undefined
[25] V8W 3V6,undefined
[26] Canada,undefined
[27] University of Victoria,undefined
[28] PO Box 1700 STN CSC,undefined
[29] Victoria,undefined
[30] British Columbia,undefined
[31] V8W 2Y2,undefined
[32] Canada,undefined
[33] Mathematics,undefined
[34] Statistics,undefined
[35] Physics,undefined
[36] and Computer Science,undefined
[37] University of British Columbia Okanagan,undefined
[38] 3333 University Way,undefined
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摘要
External beam radiation therapy is a standard form of treatment for numerous cancers. Despite this, there are no approved methods to account for patient specific radiation sensitivity. In this report, Raman spectroscopy (RS) was used to identify radiation-induced biochemical changes in human non-small cell lung cancer xenografts. Chemometric analysis revealed unique radiation-related Raman signatures that were specific to nucleic acid, lipid, protein and carbohydrate spectral features. Among these changes was a dramatic shift in the accumulation of glycogen spectral bands for doses of 5 or 15 Gy when compared to unirradiated tumours. When spatial mapping was applied in this analysis there was considerable variability as we found substantial intra- and inter-tumour heterogeneity in the distribution of glycogen and other RS spectral features. Collectively, these data provide unique insight into the biochemical response of tumours, irradiated in vivo, and demonstrate the utility of RS for detecting distinct radiobiological responses in human tumour xenografts.
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