Biologically based risk estimation for radiation-induced CML - Inferences from BCR and ABL geometric distributions

RADIVOYEVITCH, Tom, Stanislav KOZUBEK a RK SACHS. Biologically based risk estimation for radiation-induced CML - Inferences from BCR and ABL geometric distributions. Radiation and Environmental Biophysics. New York: Springer-Verlag, 2001, roč. 40, č. 1, s. 1-9. ISSN 0301-634X.

Základní údaje

• Originální název: Biologically based risk estimation for radiation-induced CML - Inferences from BCR and ABL geometric distributions
• Autoři: RADIVOYEVITCH, Tom, Stanislav KOZUBEK a RK SACHS.
• Vydání: Radiation and Environmental Biophysics, New York, Springer-Verlag, 2001, 0301-634X.

Další údaje

• Originální jazyk: angličtina
• Typ výsledku: Článek v odborném periodiku
• Obor: 10610 Biophysics
• Stát vydavatele: Spojené státy
• Utajení: není předmětem státního či obchodního tajemství
• Impakt faktor: Impact factor: 1.776
• Organizační jednotka: Přírodovědecká fakulta

Anotace

Chronic myeloid leukemia (CML) invites biologically based radiation risk modeling because CML is simultaneously well-understood, homogeneous and prevalent. CML is known to be caused by a translocation involving the ABL and BCR genes, almost all CML patients have the BCR-ABL translocation, and CML is prevalent enough that its induction is unequivocally detected among Hiroshima A-bomb survivors. In a previous paper, a linear-quadratic-exponential (LQE) dose-response model was used to estimate the lifetime excess risk of CML in the limit of low doses of gamma -rays, R-gamma. This estimate assumed that BCR-ABL translocation dose-response curves in stem cells for both neutrons and gamma -rays, differ only by a common proportionality constant from dicentric aberration dose-response curves in lymphocytes. In the present paper we challenge this assumption by predicting the BCR-ABL dose response. The predictions are based on the biophysical theory of dual radiation action (TDRA) as it applies to recent BCR-to-ABL distance data in G(0) human lymphocytes; this data shows BCR and ABL geometric distributions that are not uniform and not independent, with close association of the two genes in some cells. The analysis speaks against the previous proportionality assumption. We compute 11 plausible LQE estimates of R-gamma, 2 based on the proportionality assumption and 9 based on TDRA predictions. For each estimate of R-gamma We also compute an associated estimate of the number of CML target cells, N; the biological basis of the LQE model allows us to form such estimates. Consistency between N and hematological considerations provides a plausibility check of the risk estimates. Within the group of estimates investigated, the most plausible lifetime excess risk estimates tend to lie near R-gamma=0.01 Gy(-1), substantially higher than risk estimates based on the proportionality assumption.