Contribution of Lethal Mutations to Excision Assays for Tumour Cell Survival

References

• Seymour C B, Mothersill C, Alper T. High yields of lethal mutations in somatic mammalian cells that survive ionising radiation. Int J Radiat Biol 1986; 50: 167–79
   Web of Science ®Google Scholar
• Seymour C, Mothersill C B. All colonies of CHO-K1 cells surviving gamma-irradiation contain non-viable cells. Mutat Res 1992; 267: 19–30
   PubMed Web of Science ®Google Scholar
• Mothersill C, Seymour C. The influence of lethal mutations on the quantification of radiation transformation frequencies. Int J Radiat Biol 1987; 51: 723–9
   Web of Science ®Google Scholar
• Alper T, Mothersill C, Seymour C B. Lethal mutation attributable to misrepair of Q-lesions. Int J Radiat Biol 1988; 54: 525–30
   PubMed Web of Science ®Google Scholar
• Gorgojo L, Little J B. Expression of lethal mutations in progeny of irradiated mammalian cells. Int J Radiat Biol 1989; 55: 619–30
   PubMed Web of Science ®Google Scholar
• Mendonca M S, Kurohara W, Antoniono R, Redpath J L. Plating efficiency as a function of time post-irradiation: evidence for the delayed expression of lethal mutations. Radiat Res 1989; 119: 387–93
   PubMed Web of Science ®Google Scholar
• Chang W P, Little J B. Delayed reproductive death in x-irradiated Chinese hamster ovary cells. Int J Radiat Biol 1991; 60: 483–96
   PubMed Web of Science ®Google Scholar
• Chang W P, Lttle J B. Delayed reproductive death as a dominant phenotype in cell clones surviving x-irradiation. Carcinogenesis 1992; 13: 923–8
   PubMed Web of Science ®Google Scholar
• Born R, Trott K R. Clonogenicity of the progeny of surviving cells after irradiation. Int J Radiat Biol 1988; 53: 319–30
   Web of Science ®Google Scholar
• Little J B, Gorgojo L, Vetrovs H. Delayed appearance of lethal and specific gene-mutations in irradiated mammalian cells. Int J Radiat Oncol Biol Phys 1990; 19: 1425–9
   PubMed Web of Science ®Google Scholar
• Mendonca M S, Antoniono R J, Redpath J L. Delayed heritable damage and epigenetics in radiation-induced neoplastic transformation of human hybrid cells. Radiat Res 1993; 134: 209–16
   PubMed Web of Science ®Google Scholar
• Seymour C B, Mothersill C. Chemotherapy agents and the induction of late lethal defects. Anticancer Res 1991; 11: 1605–8
   PubMed Web of Science ®Google Scholar
• Stamato T, Weinstein R, Peters B, Hu J, Doherty B, Giaccia A. Delayed mutation in Chinese hamster cells. Somatic Cell Molec Genet 1987; 13: 57–65
   PubMedGoogle Scholar
• Puck T T, Marcus P I. Action of x-rays on mammalian cells. J Exp Med 1956; 103: 653–66
   PubMed Web of Science ®Google Scholar
• Seymour C B, Mothersill C. Lethal mutations, the survival curve shoulder and split dose recovery. Int J Radiat Biol 1989; 56: 999–1000
   PubMed Web of Science ®Google Scholar
• Pavy J J, Rojas A, Hodgkiss R J, et al. Proliferation in CaNT tumours during and after fractionated radiotherapy assessed by local control, clonogenic survival and cell kinetics. Br J Radiol 1990; 63: 587
   Google Scholar
• Hodgkiss R J. Isolation of mammalian cell variants with enhanced thiol levels after high doses of radiation. Int J Radiat Biol 1990; 57: 83–95
   PubMed Web of Science ®Google Scholar
• Moriarty M J, Mulgrew S, Malone J R, O'Connor M K. Results and analysis of tumour levels of ascorbic acid. Irish J Med Sci 1977; 146: 74–8
   PubMed Web of Science ®Google Scholar
• Revesz L, Bergstrand H, Modig H. Intrinsic non-protein sulphydryl levels and cellular radiosensitivity. Nature 1963; 198: 1275–7
   PubMed Web of Science ®Google Scholar
• Balmukhanov S B, Yefimov M L, Kleinbock T S. Acquired radioresistance of tumour cells. Nature 1967; 216: 709–11
   PubMed Web of Science ®Google Scholar
• Kadhim M A, MacDonald D A, Goodhead D T, Lorimore S A, Marsden S J, Wright E G. Transmission of chromosomal instability after plutonium α-irradiation. Nature 1992; 355: 738–40
   PubMed Web of Science ®Google Scholar
• Courtenay V D, Selby P J, Smith I E, Mills J, Peckham M J. Growth of human tumour cell colonies from biopsies using two soft-agar techniques. Br J Cancer 1978; 38: 77–81
   PubMed Web of Science ®Google Scholar
• Fertil B, Malaise E-P. Inherent cellular radiosensitivity as a basic concept for tumour radiotherapy. Int J Radiat Oncol Biol Phys 1981; 7: 621–9
   PubMed Web of Science ®Google Scholar
• Brock W A, Baker F L, Wike J L, Sivon S L, Peters L J. Cellular radiosensitivity of primary head and neck squamous cell carcinomas and local tumour control. Int J Radiat Oncol Biol Phys 1989; 18: 1283–6
   Web of Science ®Google Scholar
• West C ML, Davidson S E, Hunter R D. Evaluation of surviving fraction at 2 Gy as a potential prognostic factor for the radiotherapy of carcinoma of the cervix. Int J Radiat Biol 1989; 56: 761–5
   PubMed Web of Science ®Google Scholar