Publications by authors named "Ai-Ling Su"

Ecto-5'-nucleotidase (CD73), encoded by the NT5E gene, mediates tumor immunosuppression and has been targeted for the development of new anticancer drugs. Proteasome inhibitors impair protein degradation by inhibiting proteasome and have been used in the clinic for cancer therapy. Here we report that proteasome inhibitors reduce the protein and mRNA levels of CD73.

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  • Colorectal cancer (CRC) is a challenging disease to treat, but targeting BET proteins with specific inhibitors (BETis) shows promise in disrupting gene transcription and inhibiting CRC growth.
  • Researchers tested a combination of BET inhibitors and Tankyrase inhibitors (TNKSi) to enhance treatment effectiveness, which helped to reduce cell proliferation and induce cell death in CRC cell lines with or without mutations.
  • The combination treatment led to increased cell cycle arrest and apoptosis, suggesting that it could be a novel approach to CRC therapy, though further optimization of the strategy is necessary.
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Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited, lethal ventricular arrhythmia triggered by catecholamines. Mutations in genes that encode cardiac ryanodine receptor (RyR2) and proteins that regulate RyR2 activity cause enhanced diastolic Ca release (leak) through the RyR2 channels, resulting in CPVT. Current therapies for CPVT are limited.

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Hereditary spherocytosis (HS) is often misdiagnosed due to lack of specific diagnostic methods. Our study summarized clinical characteristics and described the diagnostic workflow for mild and moderate HS in Chinese individuals, using data from 20 adults, 8 of whom presented a familial history for HS. We used scanning electron microscopy (SEM) to diagnose HS.

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  • The study aimed to analyze the variations and importance of serum ferritin levels in Chinese patients with blood cancers, specifically hematologic malignancies.* -
  • A total of 473 patients were included, with notable diagnoses being acute leukemia, lymphoma, and multiple myeloma, and results showed higher serum ferritin levels in newly diagnosed and recurrent cases compared to those in remission.* -
  • The findings suggest that monitoring serum ferritin levels can be useful for evaluating the health status and prognosis of patients with hematologic malignancies.*
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Objective: To investigate the efficacy and safety of voriconazole in treating Chinese patients with hematological malignancies and invasive aspergillosis.

Methods: From March 2007 to April 2012, patients with diagnoses confirmed by CT, GM test and/or PCR assays, were recruited into this study. Aspergillosis of all patients were treated with voriconazole 6 mg/kg intravenous infusion (iv) every 12 h for 1 day, followed by 4 mg/kg IV every 12 h for 10-15 days; Then, switch to oral administration that was 200 mg every 12 h for 4-12 weeks.

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Objective: To study the role of promoter methylation of insulin-like growth factor binding protein 3 (IGFBP3) in intrauterine growth restriction (IUGR).

Methods: Fifty neonates with IUGR and 30 healthy neonates were enrolled. The promoter methylation status of IGFBP3 in peripheral blood was evaluated by methylation-specific PCR (MSP) and high resolution melting (HRM) techniques.

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  • The study aimed to explore the effectiveness of interphase fluorescence in situ hybridization (FISH) for identifying gene abnormalities related to chronic lymphocytic leukemia (CLL), focusing on specific genetic deletions and trisomies.
  • Out of 30 patients, 63.3% exhibited molecular cytogenetic abnormalities, with the most common being the deletion of the 13q14 region and trisomy of chromosome 12.
  • Although no significant links were found between these genetic abnormalities and most clinical factors, a higher incidence of atm gene deletion was noted in patients with high CD38 expression, indicating the need for further research into the prognostic implications of these findings.
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Objective: To study the effect of tetrandrine (Tet) in combination with droloxifen (DRL) on the expression of nuclear factor kappa B (NF-kappaB) in K562 and K562/A02 cell lines and its reversal mechanism.

Methods: The activation of NF-kappaB in K562 and K562/A02 cell lines and the effect of Tet or DRL alone or in combination on NF-kappaB protein expression were determined with immunocytochemistry and Western blotting respectively.

Results: (1) K562/A02 cells displayed higher level of NF-kappaB protein expression than K562 cells.

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Objective: To investigate the effects of tetrandrine (Tet) on nuclear factor kappaB (NF-kappaB) expression in leukemia cell line K562 and multidrug-resistant K562/A02 cell line.

Methods: The activations of NF-kappaB in K562 and K562/A02 cells and the effects of 1 micromol/L Tet on NF-kappaB expression were determined by immunocytochemistry and Western blot assay.

Results: Tet had no effect on NF-kappaB expression in K562 cells after 6- and 12-hour treatment (P>0.

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The aim of this study was to investigate the effect of nonmyeloablative peripheral blood stem cell transplantation in treatment of chronic myeloid leukemia in chronic phase (CML-CP) and accelerated phase (CML-AP). 24 patients with CML including 16 in CML-CP and 8 in CML-AP were treated with nonmyeloablative conditioning regimen for peripheral blood stem cell transplantation (PBHSCT). The conditioning regimen included fludarabine (30 mg/m(2)x6 d), busulphan [4 mg/(kg.

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Objective: To explore the therapy to further elevate the efficacy of the treatment of chronic aplastic anemia (CAA).

Methods: Forty-five patients with CCA were assigned into two groups, the 26 patients in the treated group were treated by Shengxuening (a Chinese herbal preparation) and cyclosporin A (CsA), and the 19 patients in the control group were treated with androgen alone, with the therapeutic course lasting for over 3 months. Changes of peripheral blood picture, and the colony productivity of burst forming unit-erythroid (BFU-E), colony forming unit-erythroid (CFU-E) and colony forming unit-granulocyte macrophage (CFU-GM) in bone marrow were observed before and after 3 months treatment.

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