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Translationally controlled tumor protein (TCTP) is a highly conserved multifunctional protein, which participates in many important physiological processes. Recently, the roles of TCTP in cell proliferation and apoptosis, especially its close relationship with various tumors, have attracted widespread attention. In this study, we found that the protein level of TCTP was significantly reduced in acute promyelocytic leukemia cell line NB4 transfected with retinoic acid-induced gene G (RIG-G). The RIG-G was found in our previous work as a key mediator of anti-proliferative activity in retinoid/interferon-related pathways. Here, we tried to further explore the function of TCTP in the development of acute myeloid leukemia (AML) from different levels. Our results showed that inhibiting TCTP expression could attenuate AML cells proliferation and induce apoptosis both in AML cell lines and in xenograft of NOD-SCID mice. In addition, either compared with patients in complete remission or non-leukemia patients, we detected that the expression of TCTP was generally high in the fresh bone marrow of AML patients, suggesting that there was a certain correlation between TCTP and AML disease progression. Taken together, our study revealed the role of TCTP in AML development, and provided a potential target for AML treatment.
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http://dx.doi.org/10.1016/j.cellsig.2024.111074 | DOI Listing |
Pharmacol Res Perspect
October 2025
Faculty of Health Sciences and Medicine, Bond University, Robina, Queensland, Australia.
Drug repurposing offers a cost-effective and time-efficient strategy for identifying new cancer therapies. Sertraline, a widely prescribed selective serotonin reuptake inhibitor (SSRI), has shown promising anticancer properties through modulation of key pathways involved in tumor survival, stress adaptation, and therapeutic resistance. This scoping review systematically evaluates the current evidence on sertraline's anticancer mechanisms, efficacy, and translational potential.
View Article and Find Full Text PDFAdv Exp Med Biol
July 2025
Department of Anatomy & Cell Biology, Department of Medical Science, College of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Reprogramming tumor cells to a normal state is a central issue in cancer biology. Human translationally controlled tumor protein (TCTP) has emerged as a major player in tumor reversion. However, genetic networks linked to the family of TCTP proteins are complex, and the roles of TCTP in tumor formation and reversion are only partially understood.
View Article and Find Full Text PDFPlant Sci
July 2025
College of Agriculture, Xinjiang Agricultural University, Urumqi 830001, China; College of Biotechnology, Xinjiang Agricultural Vocational and Technical University, Changji 831100, China. Electronic address:
Translationally controlled tumor proteins (TCTPs) are highly conserved proteins found in virtually all eukaryotes, and their expression is intricately linked with numerous biochemical processes and cellular activities. However, intriguingly, within the realm of key cash crops, investigations of the TCTP gene in cotton are relatively limited. This study sought to elucidate the evolutionary relationships and structural functions of the TCTP gene in cotton with a whole-genome analysis approach.
View Article and Find Full Text PDFJ Oral Biol Craniofac Res
July 2025
Faculty of Veterinary Science, Prince of Songkla University, Songkhla, 90110, Thailand.
Objective: This study aimed to enhance conventional glass ionomer cement (GIC) by incorporating 15 % chitosan, 5 % bovine serum albumin (BSA), 0.05 % tricalcium phosphate (TCP), and 1 μg translationally controlled tumor protein (TCTP), resulting in an enhanced-GIC formulation. The study evaluated its adhesion properties, biocompatibility, and ability to promote pulp tissue healing in rabbit anterior teeth.
View Article and Find Full Text PDFJ Oral Sci
July 2025
Department of Oral Biology and Occlusion, Faculty of Dentistry, Prince of Songkla University.
Purpose: This study aimed to investigate the minimum inhibitory concentration (MIC) and biological properties of modified glass-ionomer cement (BIO-GIC) supplemented with chlorhexidine diacetate (CHX).
Methods: The BIO-GIC was originally a combining formulation of conventional glass-ionomer cement, chitosan, albumin and tricalcium phosphate. CHX was incorporated at various concentrations of 1.