Publications by authors named "Xiang-Mei Ye"

Article Synopsis
  • Imatinib resistance in chronic myeloid leukaemia (CML) is linked to the activation of the Lyn/BCR-ABL/SIRT1 signaling pathway, which inhibits important proteins like Ac-Foxo1 and p53, reducing cell apoptosis.
  • Research methods included cell viability tests, apoptosis measurement through flow cytometry, and the use of a CML mouse model, confirming the role of SIRT1 and Lyn in resistance to imatinib.
  • The study concluded that targeting SIRT1 may enhance the effectiveness of imatinib treatment in CML by promoting apoptosis and inhibiting growth of resistant cancer cells.
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Polymorphisms in arsenic (+ 3 oxidation state) methyltransferase (AS3MT) have been shown to be related to interindividual variations in arsenic metabolism and to influence adverse health effects in acute promyelocytic leukemia (APL) patients treated with arsenic trioxide (AsO). The occurrence of hyperleukocytosis with AsO treatment seriously affects the early survival rate of APL patients, but no definite explanation for such a complication has been clearly established. To clarify the causes of this situation, AS3MT polymorphisms 14215 (rs3740390), 14458 (rs11191439), 27215 (rs11191446), and 35991 (rs10748835) and profiles of plasma arsenic metabolites were evaluated in a group of 54 newly diagnosed APL patients treated with single-agent AsO.

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The human serotonin receptor 1B (HRT1B) plays an important role in regulating serotonin release. Previous research has suggested that the genetic variation of the HTR1B gene may confer susceptibility to alcoholism or some subtypes of alcohol dependence, but the evidence has been inconsistent. The aim of the present study is to examine whether polymorphic variants of the HTR1B gene are associated with alcohol dependence subtypes or drinking-related behaviors in Chinese Han population.

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