PMID- 23998577 OWN - NLM STAT- MEDLINE DCOM- 20140501 LR - 20181023 IS - 1009-2137 (Print) IS - 1009-2137 (Linking) VI - 21 IP - 4 DP - 2013 Aug TI - Expression of PML-RARalpha is up-regulated during ATRA and arsenics combined induction without influence on long-term prognosis of acute promyelocytic leukemia. PG - 872-8 LID - 10.7534/j.issn.1009-2137.2013.04.012 [doi] AB - The early molecular kinetics during all-trans retinoic acid (ATRA) plus arsenic-based induction therapy and its prognostic value for acute promyelocytic leukemia (APL) remain unclear. This study was purposed to investigate the molecular and cytogenetic kinetics and its clinical significance in treatment of APL with ATRA plus arsenic-based induction. The molecular and cytogenetic kinetics was assessed by real-time quantitative RT-PCR and interphase fluorescence in situ hybridization (FISH) in 32 newly diagnosed APL patients. The results showed that the median PML-RARalpha transcript levels (PML-RARalpha/ABL) were very significantly up-regulated at 14 days of induction therapy compared with that of pre-treatment (40.10% vs 57.74%, P < 0.01), and then decreased at 28 days of induction therapy and at the end of consolidation therapy (6.97% and 0%), respectively. The total of 65.62% and 31.25% patients showed up-regulation of PML-RARalpha transcript at 14 and 28 days after induction, as compared with pretreatment. The PML-RARalpha copies per APL cell before treatment, and at 14 and 28 days after induction were calculated as 0.9, 2.2, 1.4 by the formula of PML-RARA/ABL(%)x2/APL cells (%). With the median follow-up time of 22 months, 32 patients were still in continuous clinical remission and no molecular relapse occurred. Up-regulation of PML-RARa expression during the induction had no effect on outcomes of APL patients. It is concluded that up-regulation of PML-RARa expression is a common event during induction therapy with ATRA plus arsenics. Up-regulation of PML-RARa expression during induction therapy hasn't influenced the long-term prognosis of APL. FAU - Zhu, Hong-Hu AU - Zhu HH AD - Department of Hematology, Peking University People's Hospital; Peking University Institute of Hematology, Beijing 100044, China. FAU - Qin, Ya-Zhen AU - Qin YZ FAU - Lai, Yue-Yun AU - Lai YY FAU - Shi, Hong-Xia AU - Shi HX FAU - Liu, Yan-Rong AU - Liu YR FAU - Jiang, Bin AU - Jiang B FAU - Huang, Xiao-Jun AU - Huang XJ LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - China TA - Zhongguo Shi Yan Xue Ye Xue Za Zhi JT - Zhongguo shi yan xue ye xue za zhi JID - 101084424 RN - 0 (Arsenicals) RN - 0 (Oncogene Proteins, Fusion) RN - 0 (promyelocytic leukemia-retinoic acid receptor alpha fusion oncoprotein) RN - 5688UTC01R (Tretinoin) SB - IM MH - Adolescent MH - Adult MH - Antineoplastic Combined Chemotherapy Protocols/*therapeutic use MH - Arsenicals/administration & dosage MH - Female MH - Humans MH - Leukemia, Promyelocytic, Acute/diagnosis/drug therapy/*metabolism MH - Male MH - Middle Aged MH - Oncogene Proteins, Fusion/*metabolism MH - Prognosis MH - Tretinoin/administration & dosage MH - Up-Regulation/drug effects MH - Young Adult EDAT- 2013/09/04 06:00 MHDA- 2014/05/03 06:00 CRDT- 2013/09/04 06:00 PHST- 2013/09/04 06:00 [entrez] PHST- 2013/09/04 06:00 [pubmed] PHST- 2014/05/03 06:00 [medline] AID - 1009-2137(2013)04-0872-07 [pii] AID - 10.7534/j.issn.1009-2137.2013.04.012 [doi] PST - ppublish SO - Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2013 Aug;21(4):872-8. doi: 10.7534/j.issn.1009-2137.2013.04.012.