Prasit Chanarat
Chiang Mai University
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Archives of Pharmacal Research | 2006
Songyot Anuchapreeda; Pattra Thanarattanakorn; Somjai Sittipreechacharn; Singkome Tima; Prasit Chanarat; Pornngarm Limtrakul
When patients with cancers are treated with chemotherapeutic agents a long time, some of the cancer cells develop the multidrug resistance (MDR) phenotype. MDR cancer cells are characterized by the overexpression of multidrug resistance1 (MDR1) gene which encodes P-glycoprotein (Pgp), a surface protein of tumor cells that functions to produce an excessive efflux and thereby an insufficient intracellular concentration of chemotherapeutic agents. A variety of studies have sought potent MDR modulators to decreaseMDR1 gene expression in cancer cells. Our previous study has shown that curcumin exhibits characteristics of a MDR modulator in KB-V1 multidrug-resistant cells. The aim of this study was to further investigate the effect of curcumin onMDR1 gene expression in patient leukemic cells. The leukemic cells were collected from 78 childhood leukemia patients admitted at maharaj Nakorn Chiang Mai Hospital, Chiang Mai, Thailand, in the period from July 2003 to February 2005. There were 61 cases of acute lymphoblastic leukemia (ALL), 14 cases of acute myeloblastic leukemia (AML), and 3 cases of chronic myelocytic leukemia (CML). There were 47 males and 31 females ranging from 1 to 15 years old. Bone marrows were collected. The leukemic cells were separated and cultured in the presence or absence of 10 μM curcumin for 48 hours. MDR1 mRNA levels were determined by RT-PCR. It was found that curcumin reducedMDR1 gene expression in the cells from 33 patients (42%). Curcumin affected theMDR1 gene expression in 5 of 11 relapsed cases (45%), 10 of 26 cases of drug maintenance (38%), 7 of 18 cases of completed treatment (39%), and 11 of 23 cases of new patients (48%). The expression levels ofMDR1 gene in leukemic patient cells as compared to that of KB-V1 cells were classified as low level (1–20%) in 5 of 20 cases (25%), medium level (21–60%) in 14 of 32 cases (44%), and high level (61–100%) in 14 of 20 cases (70%). In summary, curcumin decreased MDR1 mRNA level in patient leukemic cells, especially in high level ofMDR1 gene groups. Thus, curcumin treatment may provide a lead for clinical treatment of leukemia patients in the future.
Acta Pharmacologica Sinica | 2006
Songyot Anuchapreeda; Pattra Thanarattanakorn; Somjai Sittipreechacharn; Prasit Chanarat; Pornngarm Limtrakul
Chiang Mai Medical Journal - เชียงใหม่เวชสาร | 2012
Nantaya Chanarat; Suchada Tawarat; Prasit Chanarat
The Bulletin of Chiang Mai Associated Medical Sciences | 2004
Kanokkan Kaewprom; Yuttana Mundee; Prasit Chanarat; Sakorn Pornprasert
The Bulletin of Chiang Mai Associated Medical Sciences | 2002
Prasit Chanarat; Nantaya Chanarat
The Bulletin of Chiang Mai Associated Medical Sciences | 2001
Mongkol Chotayaporn; Nutjeera Intasai; Prasit Chanarat
The Bulletin of Chiang Mai Associated Medical Sciences | 2001
์ีNatjira Intasai; Kamol Yoosook; Prasit Chanarat
The Bulletin of Chiang Mai Associated Medical Sciences | 2001
Prasit Chanarat
Southeast Asian Journal of Tropical Medicine and Public Health | 2001
Nantaya Chanarat; Prasit Chanarat; Kamolmarl Viratsethasin; Maitree Suttajit; Damrong Chiewsilp
The Bulletin of Chiang Mai Associated Medical Sciences | 2000
Prasit Chanarat