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SKping cell cycle regulation: role of ubiquitin ligase SKP2 in hematological malignancies.
William, Jonahunnatha Nesson George; Dhar, Ruby; Gundamaraju, Rohit; Sahoo, Om Saswat; Pethusamy, Karthikeyan; Raj, A F P Allwin Mabes; Ramasamy, Subbiah; Alqahtani, Mohammed S; Abbas, Mohamed; Karmakar, Subhradip.
Afiliação
  • William JNG; Department of Medical, Oral and Biotechnological Sciences (DSMOB), Ageing Research Center and Translational Medicine-CeSI-MeT, "G. d'Annunzio" University Chieti-Pescara, Chieti, Italy.
  • Dhar R; Department of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.
  • Gundamaraju R; ER Stress and Intestinal Mucosal Biology Lab, School of Health Sciences, University of Tasmania, Launceston, TAS, Australia.
  • Sahoo OS; Department of Biotechnology, National Institute of Technology, Durgapur, India.
  • Pethusamy K; Department of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.
  • Raj AFPAM; Institute of Environmental Protection and Sensors (IOS), Maribor, Slovenia.
  • Ramasamy S; Cardiac Metabolic Disease Laboratory, Department Of Biochemistry, School of Biological Sciences, Madurai Kamaraj University, Madurai, India.
  • Alqahtani MS; Radiological Sciences Department, College of Applied Medical Sciences, King Khalid University, Abha, Saudi Arabia.
  • Abbas M; BioImaging Unit, Space Research Centre, University of Leicester, Leicester, United Kingdom.
  • Karmakar S; Electrical Engineering Department, College of Engineering, King Khalid University, Abha, Saudi Arabia.
Front Oncol ; 14: 1288501, 2024.
Article em En | MEDLINE | ID: mdl-38559562
ABSTRACT
SKP2 (S-phase kinase-associated protein 2) is a member of the F-box family of substrate-recognition subunits in the SCF ubiquitin-protein ligase complexes. It is associated with ubiquitin-mediated degradation in the mammalian cell cycle components and other target proteins involved in cell cycle progression, signal transduction, and transcription. Being an oncogene in solid tumors and hematological malignancies, it is frequently associated with drug resistance and poor disease outcomes. In the current review, we discussed the novel role of SKP2 in different hematological malignancies. Further, we performed a limited in-silico analysis to establish the involvement of SKP2 in a few publicly available cancer datasets. Interestingly, our study identified Skp2 expression to be altered in a cancer-specific manner. While it was found to be overexpressed in several cancer types, few cancer showed a down-regulation in SKP2. Our review provides evidence for developing novel SKP2 inhibitors in hematological malignancies. We also investigated the effect of SKP2 status on survival and disease progression. In addition, the role of miRNA and its associated families in regulating Skp2 expression was explored. Subsequently, we predicted common miRNAs against Skp2 genes by using miRNA-predication tools. Finally, we discussed current approaches and future prospective approaches to target the Skp2 gene by using different drugs and miRNA-based therapeutics applications in translational research.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Oncol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália País de publicação: Suíça