سابقه و هدف: تست هاي سيتوژنتيك براي سنجش حساسيت پرتويي و ريسك ابتلا به سرطان به كار برده مي شوند. هدف ما بررسي حساسيت پرتويي افراد سالم و بيماران مبتلا به سرطان پروستات با روش تراكم پيش رس كروموزومي (PCC) شيميايي بوده است.
مواد و روش ها: از 10 بيمار مبتلا به سرطان پروستات و 10 فرد سالم ، 3/5 ميلي ليتر خون وريدي دريافت و در 7 ميكروتيوب استريل قرار داده شد. نمونه هاي دوگروه به جز شاهد با شتاب دهنده Siemens در انرژي MV 6 دوزهاي 0/25، 0/5، 1، 2، 4 و 6 گري دريافت كردند. براي هر نمونه تست PCC شيميايي انجام و لام هاي حاصله شمارش شد. براي مقايسه ميزان بيراهي ناشي از دوزهاي مختلف در هر گروه و مقايسه بيراهي حاصل از دوزهاي يكسان در دو گروه از تست هاي Kruskal-Wallis non-parametric ANOVA و Mann-Whitney استفاده شد.
يافته ها: بين تعداد حلقه هاي ايجاد شده و دوز پرتودهي (Gy5/0≤) ارتباط معني داري در دو گروه سالم و مبتلا به سرطان بودكه با افزايش دوز، حلقه ها افزايش مي يافت (0/05
چكيده لاتين :
Background and purpose: Cytogenetic tests are used to assess the individual’s radiosensitivity
and the potential to develop cancerous diseases. Our aim was to assess the radiosensitivity of patients
with prostate cancer and healthy individuals based on Premature Chromosome Condensation (PCC).
Materials and methods: 3.5 ml blood was collected from peripheral veins of 10 healthy
individuals and 10 patients with prostate cancer and put into 7 sterile microtubes. All samples, except the
controls, were irradiated to 6MV beams of a Siemens LINAC at different doses (0.25, 0.5, 1, 2, 4 and 6
Gy). Chemical PCC test was performed on each sample and the prepared slides were scored. The
Kruskal-Wallis non-parametric ANOVA and Mann-Whitney statistical tests were used to compare the
chromosomal aberrations resulted from different dose levels in each group (healthy/cancerous), and
identical doses resulted from the two groups, respectively.
Results: There was a significant correlation between irradiation dose (for doses ≥0.5 Gy) and the
rings in both of the healthy and prostate cancer patients indicating an increase in the number of rings with
dose escalation (P<0.05). Comparing healthy individuals and cancerous patients revealed no significant
difference in their ring number at the same level of radiation doses (P= 0.784).
Conclusion: In theory, PCC test should be capable of determining more chromosomal
aberrations than dicentric test, so, if the FISH test is used simultaneously, we might be able to score
dicentrics and other fragments. By these, it may also be possible to better differentiate the radiosensitivity
of healthy individuals and prostate cancer patients.