Yerevan State University, Yerevan, Armenia.
Neurochem Res. 2010 Apr;35(4):598-602. doi: 10.1007/s11064-009-0104-8. Epub 2009 Dec 1.
A new proline-rich polypeptide (PRP-1) has been earlier shown to possess a broad spectrum of biological activities and seems to be a potential medicine. The potential genotoxic properties of PRP-1 and protective effect of PRP-1 against genotoxic action of Mitomycin C (MMC) were analyzed in details in the present work. DNA and chromosome damages were studied in KCL-22 cell line of human myeloid leukemia by the Comet assay and micronucleus induction test, respectively. The results suggest that DNA damages are, at least partly, transient and reparable. PRP-1 at the doses 0.5-2.0 microg/ml does not possess genotoxic activity. Moreover, this peptide expresses both preventive and therapeutic effects against MMC-induced DNA damage. Pre-treatment of cells with PRP-1 also prevents the appearance of daughter cells bearing as heavy MMC-induced DNA/chromosome damages as MNs. Thus, the polypeptide studied is able to protect the cells from genotoxic action of MMC. This defense includes not only DNA but also heritable chromosome damage in post-mitotic cells. Possible mechanisms of PRP-1 protective action are discussed.
一种新的脯氨酸丰富多肽(PRP-1)具有广泛的生物学活性,似乎是一种有潜力的药物。本研究详细分析了 PRP-1 的潜在遗传毒性特性及其对丝裂霉素 C(MMC)遗传毒性作用的保护作用。通过彗星试验和微核诱导试验,分别在人髓性白血病 KCL-22 细胞系中研究了 DNA 和染色体损伤。结果表明,DNA 损伤至少部分是短暂的和可修复的。PRP-1 在 0.5-2.0μg/ml 的剂量下不具有遗传毒性活性。此外,该肽对 MMC 诱导的 DNA 损伤具有预防和治疗作用。PRP-1 的预处理还可防止出现带有与 MN 一样重的 MMC 诱导的 DNA/染色体损伤的子细胞。因此,所研究的多肽能够保护细胞免受 MMC 的遗传毒性作用。这种防御不仅包括 DNA,还包括有丝分裂后细胞的遗传性染色体损伤。讨论了 PRP-1 保护作用的可能机制。