RESUMEN

Y box binding protein 1 (YB-1) is a protein with a highly conserved cold shock domain (CSD) that also belongs to the family of DNA- and RNA-binding proteins. YB-1 is present in both the nucleus and cytoplasm and plays versatile roles in gene transcription, RNA splicing, DNA damage repair, cell cycle progression, and immunity. Cumulative evidence suggests that YB-1 promotes the progression of multiple tumor types and serves as a potential tumor biomarker and therapeutic target. This review comprehensively summarizes the emerging functions, mechanisms, and regulation of YB-1 in cancers, and further discusses targeted strategies.

Asunto(s)

Proteínas Oncogénicas , Proteína 1 de Unión a la Caja Y , Núcleo Celular/metabolismo , Proteínas de Unión al ADN/metabolismo , Proteínas Oncogénicas/metabolismo , Procesamiento Proteico-Postraduccional , Proteína 1 de Unión a la Caja Y/genética , Proteína 1 de Unión a la Caja Y/metabolismo

RESUMEN

Basal-like breast cancer (BLBC) is the most aggressive subtype of breast cancer with a poor prognosis. Long noncoding RNAs (lncRNAs) play critical roles in human cancers. Krüppel-like Factor 5 (KLF5) is a key oncogenic transcription factor in BLBC. However, the underlying mechanism of mutual regulation between KLF5 and lncRNA remains largely unknown. Here, we demonstrate that lncRNA KPRT4 promotes BLBC cell proliferation in vitro and in vivo. Mechanistically, KLF5 directly binds to the promoter of KPRT4 to promote KPRT4 transcription. Reciprocally, KPRT4 recruits the YB-1 transcription factor to the KLF5 promoter by interacting with YB-1 at its 5' domain and forming an RNA-DNA-DNA triplex structure at its 3' domain, resulting in enhanced transcription of KLF5 and ultimately establishing a feedforward circuit to promote cell proliferation. Moreover, the antisense oligonucleotide (ASO)-based therapy targeting KPRT4 substantially attenuated tumor growth in vivo. Clinically, the expression levels of YB-1, KLF5 and KPRT4 are positively correlated in clinical breast specimens. Together, our data suggest that KPRT4 is a major molecule for BLBC progression and that the feedforward circuit between KLF5 and KPRT4 may represent a potential therapeutic target in BLBC.

Asunto(s)

Neoplasias de la Mama , Factores de Transcripción de Tipo Kruppel , ARN Largo no Codificante , Neoplasias de la Mama/patología , Línea Celular Tumoral , Proliferación Celular/genética , Femenino , Regulación Neoplásica de la Expresión Génica , Humanos , Factores de Transcripción de Tipo Kruppel/genética , Factores de Transcripción de Tipo Kruppel/metabolismo , ARN Largo no Codificante/genética , Factores de Transcripción/genética

RESUMEN

Smart chromic elastomers exhibiting multistimuli responsiveness are of interest with regard to the development of sensors, optical data storage, and smart wearable devices. We report a new design of Cu nanoclusters (Cu NCs) containing polymeric elastomer film, showing reversible fluorescence ON/OFF when subjected to organic solvents (e.g. ethanol, methanol and tetrahydrofuran), and heating/cooling cycles at temperatures lower than 80 °C. Different from the solvato-responsiveness of Cu NCs in solution state, organic solvents increase nonradiative decay and quench fluorescence emission in the solid polymer matrix. It is deduced that lower temperatures (<80 °C) increase reversible nonradiative decay, while higher temperatures (>80 °C) trigger an irreversible change of the aggregation state of Cu NCs in the elastomer film. A strong oxidizer (e.g. H2O2) irreversibly quenches the fluorescence emission and changes its color (under sunlight) from light green to blue, by oxidizing Cu NCs to Cu2+ ions. This Cu NC-containing elastomer film illustrates a new pathway to the fabrication of multi-responsive smart optical materials, particularly for potential applications in optical data storage (e.g. thermo-printing), and multistimuli-responsive elastomeric sensors integrated into wearable devices.

RESUMEN

Fluorochromic materials that change their emission properties in response to their environment are of interest for the development of sensors, optical data storage and light-emitting materials. A thermally fluorochromic elastic polymer film that exhibits remarkable fluorochromism (from red to yellow) and enhancement of fluorescence intensity after thermal treatment (>120 °C) is designed by the incorporation of silver nanoclusters. The thermal treatment also leads to a significant increase of quantum yield and fluorescence lifetime. It is found that the thermo-induced etching on larger silver nanoclusters generates smaller silver nanoclusters. This simple and efficient size-tuning process in solid state is responsible for the thermo-fluorochromism and enhancement of fluorescence emission from silver nanoclusters. Such a thermo-fluorochromic polymer material is finally demonstrated to be useful for thermo-printing. This material illustrates a new way to make smart optical materials, particularly for potential applications in optical data storage and soft OLED display.