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Emerging Molecular Mechanisms of Cell Cycle Regulation: Opportunities for Cancer Intervention?

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Oncology".

Deadline for manuscript submissions: closed (15 March 2023) | Viewed by 2326

Special Issue Editors


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Guest Editor
Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117600, Singapore
Interests: cancer pharmacology; precision oncology; cell metabolism; genetic cancer predisposition; upper aerodigestive tract cancers

E-Mail Website
Guest Editor
Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117600, Singapore
Interests: haematology; medical oncology

Special Issue Information

Dear Colleagues,

Deregulation of cell cycle has long been regarded as a key feature of oncogenesis, and is critical for sustained proliferation and uncontrolled cell division in tumors. Inhibitors of cell cycle checkpoints have been investigated as cancer therapy, but adverse toxicities have impeded further development. Recently, the breakthrough of cyclin-dependent kinase inhibitors in breast cancer therapy has rekindled the interest in the field. Unravelling the molecular underpinnings of cell cycle regulators, such as the crosstalk with oncogenes and tumor suppressors, may expose mechanisms for cancer progression. Moreover, the advances in single-cell technologies and multi-omics technologies have yielded an unprecedented platform for the understanding of cell cycle biology.

This Special Issue, “Emerging Molecular Mechanisms of Cell Cycle Regulation: Opportunities for Cancer Intervention?” aims to cover emerging evidence of cell cycle perturbations in cancer cells, and to discuss potential therapeutic strategies that cover cancer research. Original research articles and review articles on aspects relevant to cell cycle regulation, including but not limited to cancer cell biology, drug discovery/target validation, drug combinations, and genomics/genetics, are welcome for submission to this Special Issue.

Dr. Li Ren Kong
Dr. Andrea L. Wong
Guest Editors

Manuscript Submission Information

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Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. International Journal of Molecular Sciences is an international peer-reviewed open access semimonthly journal published by MDPI.

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Keywords

  • cell cycle regulators
  • molecular targets
  • prognosis biomarkers
  • cancer cell susceptibility
  • synthetic lethality
  • tumour heterogeneity
  • clinical drug development

Published Papers (1 paper)

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Research

11 pages, 3685 KiB  
Article
Tumor-Promoting Actions of HNRNP A1 in HCC Are Associated with Cell Cycle, Mitochondrial Dynamics, and Necroptosis
by Biao Zhao, Xiaochen Lv, Xiaoqi Zhao, Subinuer Maimaitiaili, Yuheng Zhang, Ke Su, Hang Yu, Cheng Liu and Tong Qiao
Int. J. Mol. Sci. 2022, 23(18), 10209; https://doi.org/10.3390/ijms231810209 - 06 Sep 2022
Cited by 7 | Viewed by 2023
Abstract
Hepatocellular carcinoma (HCC) is one of the most frequent malignancies in the world. Although increasing evidence supports the role of heterogeneous ribonucleoprotein particle A1 (HNRNP A1) in tumor progression, the function of HNRNP A1 in HCC remains unclear. Here, we focused on the [...] Read more.
Hepatocellular carcinoma (HCC) is one of the most frequent malignancies in the world. Although increasing evidence supports the role of heterogeneous ribonucleoprotein particle A1 (HNRNP A1) in tumor progression, the function of HNRNP A1 in HCC remains unclear. Here, we focused on the role of HNRNP A1 in the development of HCC. In this study, we found HNRNP A1 participates in many aspects of HCC, such as progression and prognosis. Our results showed that HNRNP A1 is upregulated in human HCC tissues and cell lines. High expression of HNRNP A1 can promote the proliferation, migration, and invasion in HCC cells and accelerate tumor progression in mice. Moreover, we found that HNRNP A1 prevents the senescence process of HCC cells. Knocking down of HNRNP A1 promotes the expression of P16INK4, which arrests the cell cycle and then induces the senescence phenotype in HCC cells. Furthermore, we found that HNRNP A1 regulated necroptosis and mitochondrial dynamics. In summary, our study indicates that HNRNP A1 promotes the development of HCC, which suggests a potential therapeutic target for HCC. Full article
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