Fiona Lyng

Prof. Fiona Lyng

Radiation and Environmental Science Centre, Focas Research Institute, Technological University Dublin, D08 NF82 Dublin, Ireland
orcid

Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 2007 in Toxicology in Vitro
Verified
Journal Article
Closed access
MDMaria Davoren
Maria Davoren
EHEva Herzog
Eva Herzog
ACAlan Casey
Alan Casey
BCBenjamin Cottineau
Benjamin Cottineau
GCGordon Chambers
Gordon Chambers
Fiona LyngFiona Lyng
Fiona Lyng

1 June 2007 in Carbon
Verified
Journal Article
Closed access
ACA. Casey
A. Casey
EHE. Herzog
E. Herzog
MDM. Davoren
M. Davoren
Fiona LyngFiona Lyng
Fiona Lyng
Hugh ByrneHugh Byrne
Hugh Byrne
GCG. Chambers
G. Chambers

1 November 2000 in British Journal of Cancer
Verified
Journal Article
Open access
PDF file
Fiona LyngFiona Lyng
Fiona Lyng
CSC B Seymour
C B Seymour
CMC Mothersill
C Mothersill
This study investigated the ability of medium from irradiated cells to induce early events in the apoptotic cascade, such as mobilization of intracellular calcium, loss of mitochondrial membrane potential and increase in reactive oxygen species, in cells which were never exposed to radiation. Medium from irradiated human keratinocytes was harvested and transferred to unirradiated keratinocytes. Endpoints characteristic of the initiation of apoptosis were monitored for a period of 24 h following medium transfer. Clonogenic survival was also measured. Rapid calcium fluxes (within 30 s), loss of mitochondrial membrane potential, increases in reactive oxygen species (from 6 h after medium transfer), an increase in the number of apoptotic cells (48 hours after medium transfer) and a marked reduction in clonogenic survival (after 9 days) were observed. There was no significant difference between medium generated by cells irradiated at 0.5 Gy or 5 Gy. The data suggest that initiating events in the apoptotic cascade were induced in unexposed cells by a signal produced by irradiated cells. © 2000 Cancer Research Campaign

1 November 2007 in Toxicology Letters
Verified
Journal Article
Closed access
EHE Herzog
E Herzog
ACA Casey
A Casey
Fiona LyngFiona Lyng
Fiona Lyng
GCG Chambers
G Chambers
Hugh ByrneHugh Byrne
Hugh Byrne
MDM Davoren
M Davoren

1 July 2005 in Vibrational Spectroscopy
Verified
Journal Article
Closed access
EFEoghan Ó Faoláin
Eoghan Ó Faoláin
MHMary B. Hunter
Mary B. Hunter
JBJoe M. Byrne
Joe M. Byrne
PKPeter Kelehan
Peter Kelehan
MMMary McNamara
Mary McNamara
Fiona LyngFiona Lyng
Fiona Lyng

1 April 2002 in Radiation Research
Verified
Journal Article
Closed access
Fiona LyngFiona Lyng
Fiona Lyng
CSC. B. Seymour
C. B. Seymour
CMC. Mothersill
C. Mothersill
Genomic instability and bystander effects have recently been linked experimentally both in vivo and in vitro. The aim of the present study was to determine if medium from irradiated cells several passages distant from the original exposure could initiate apoptosis in unirradiated cells. Human keratinocytes (from the HPV-G cell line) were irradiated with 0.5 Gy or 5 Gy gamma rays. Medium was harvested at each passage up to the 7th passage (approximately 35 population doublings) postirradiation and transferred to unirradiated keratinocytes. Intracellular calcium levels, mitochondrial membrane potential, and the level of reactive oxygen species were all monitored for 24 h after medium transfer. Rapid calcium fluxes (within 30 s), loss of mitochondrial membrane potential, and increases in reactive oxygen species (from 6 h after medium transfer) were observed in the recipient cells. There was no significant difference between medium conditioned by cells irradiated with 0.5 or 5 Gy. The effect of medium from progeny was the same as the initial effect reported previously and did not diminish with increasing passage number. The data suggest that initiating events in the cascade that leads to apoptosis are induced in unirradiated cells by a signal produced by irradiated cells and that this signal can still be produced by the progeny of irradiated cells for several generations.