Publications by authors named "Meng-Jie Fu"

Epigenetics refers to the reversible process through which changes in gene expression occur without changing the nucleotide sequence of DNA. The process is currently gaining prominence as a pivotal objective in the treatment of cancers and other ailments. Numerous drugs that target epigenetic mechanisms have obtained approval from the Food and Drug Administration (FDA) for the therapeutic intervention of diverse diseases; many have drawbacks, such as limited applicability, toxicity, and resistance.

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Article Synopsis
  • Lysine specific demethylase 1 (LSD1) is a key transcriptional modulator that is commonly overexpressed in various cancers, disrupting normal gene expression networks.
  • Over 10 LSD1 inhibitors, including eight irreversible and two reversible types, have been developed and some have reached clinical trials, often showing better results when used with other treatments.
  • The review discusses the potential of combining LSD1 inhibitors with other cancer therapies, highlights new multitarget inhibitors, and addresses challenges and future research directions in developing LSD1-targeted cancer treatments.*
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Carbon dots (CDs) are popular as fluorescence sensors, and metal ions are typical analytes. However, CDs used as fluorescent sensors for Fe have some interferences coming from co-existed ions. In this study, we suspect that sp boron atom in phenylboronic acid group will be more compatible with Fe to form coordination bonds, thereby increasing the selectivity to Fe.

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Red emissive B,N co-doped carbon dots (BN-CDs) were hydrothermally synthesized from cresyl violet and boric acid. The BN-CDs exhibited excellent photostability, low cytotoxicity, excitation/emission maxima at 520/616 nm, and a relatively high quantum yield of 18%. The BN-CDs can binded to mercury(II), and this results in quenching of the red-colored fluorescence.

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