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Çѱ¹È¯°æ»ý¹°ÇÐȸ / v.23, no.1, 2005³â, pp.21-26
MCF-7 ¼¼Æ÷ÁÖÀÇ ¥ã¼±¿¡ ÀÇÇÑ DNA ¼Õ»ó ¹ÝÀÀ À¯ÀüÀÚ ¹ßÇö ¾ç»óÀÇ ºÐ¼®
( A DNA-Damage Response Gene Expression Analysis in MCF-7 followed by ¥ã-Radiation )
¹ÚÁöÀ±;ȲâÀÏ;¹Ú¿õ¾ç;±èÁø±Ô;俵±Ô; ÇѾç´ëÇб³ »ýÈ­ÇÐ ¹× ºÐÀÚ»ý¹°Çаú;¼­¿ï´ëÇб³ Àǰú´ëÇÐ »ýÈ­Çб³½Ç;¼­¿ï´ëÇб³ Àǰú´ëÇÐ »ýÈ­Çб³½Ç;Çѱ¹¿øÀڷ¿¬±¸¼Ò µ¿À§¿ø¼Ò ¹æ»ç¼± ÀÀ¿ëÆÀ;ÇѾç´ëÇб³ »ýÈ­ÇÐ ¹× ºÐÀÚ»ý¹°Çаú;
 
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Cell response to genotoxic agents is complex and involves the participation of different classes of genes including cell cycle control, DNA repair and apoptosis. In this report, we presented a approach to characterize the cellular functions associated with the altered transcript profiles of MCF-7 exposed to low-dose in vitro gamma-irradiation. We used the method of human 2.4 k cDNA microarrays containing apoptosis, cell cycle, chromatin, repair, stress and chromosome genes to analyze the differential gene expression characterization that were displayed by radiation-exposed cell, human breast carcinoma MCF-7 cell line, such as 4 Gy 4 hr, 8 Gy 4 hr, and 8 Gy 12 hr. Among these genes, 66 were up-regulated and 49 were down-regulated. Specific genes were concomitantly induced in the results. Cyclin dependent kinase 4 (Cdk4) is induced for starting the cell cycle. This regulation is required for a DNA damage¡©induced G1 arrest. In addition to, an apoptotic pathways gene Bcl-w was concomitantly induced. Mismatch repair protein homologue-l (hMLH1), a necessary component of DNA mismatch protein repair (MMR), in G2-M cell cycle checkpoint arrest. The present study provides new information on the molecular mechanism underlying the cell response to genotoxic stress, with relevance to basic and clinical research.
 
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irradiation;MCF-7;DNA-damage response;gene expression;
 
ȯ°æ»ý¹° / v.23, no.1, 2005³â, pp.21-26
Çѱ¹È¯°æ»ý¹°ÇÐȸ
ISSN : 1226-9999
UCI : G100:I100-KOI(KISTI1.1003/JNL.JAKO200516610524612)
¾ð¾î : Çѱ¹¾î
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