IMR Press / FBL / Special Issues / cell_cycle

Cell Cycle Modifications in Development and Cancer

Submission deadline: 31 December 2026
Special Issue Editor
  • Jacek Kubiak, PhD
    Institute of Genetics and Development of Rennes (IGDR), UMR 6290 CNRS/University of Rennes, Faculty of Medicine, Rennes, France
    Interests: cell cycle; embryo development; gonad development; cell differentiation; cancer; cell proliferation; stem cells; macrophages
Special Issue Information

Dear Colleagues,

The cell cycle undergoes distinct modifications during embryo development and cancer, reflecting different biological functions and deviations from the classical cell cycle of somatic cells.

In early embryonic development of numerous organisms, cell cycles are remarkably rapid and simplified. Following fertilization, embryos undergo cleavage divisions characterized by shortened or absent gap phases (G1 and G2), allowing cells to alternate quickly between DNA synthesis (S phase) and mitosis (M phase). These early embryonic cycles lack the stringent checkpoint controls present in somatic cells, enabling rapid cell division without growth. As development progresses, gap phases gradually lengthen, and checkpoint mechanisms become more robust, allowing cells to respond to developmental signals and differentiation mechanisms.

In contrast, cancer cells exhibit aberrant cell cycle regulation that promotes uncontrolled proliferation. Key modifications include loss of checkpoint control, particularly at the G1/S restriction point, often through mutations in tumor suppressors such as p53 and Rb. Oncogenic activation of cyclins and cyclin-dependent kinases (CDKs) drives cells through cycle checkpoints regardless of DNA damage or growth signals. Cancer cells may also bypass senescence and ignore contact inhibition signals that normally halt division.

Interestingly, both contexts involve overriding normal cell cycle constraints - embryonic cells for necessary development, and cancer cells through pathological mutations. However, embryonic modifications are tightly regulated and temporary, reverting back to checkpoint-controlled cycling as development proceeds, while cancer cells sustain these alterations indefinitely, leading to tumor formation and progression.

In this Special Issue, we welcome original and review articles related to these various cell cycle modifications.

Jacek Kubiak
Guest Editor

Keywords
cell cycle
cell division
cell signalling
embryos
cancer
cell cycle-related mutations
Manuscript Submission Information

Manuscripts should be submitted via our online editorial system at https://imr.propub.com by registering and logging in to this website. Once you are registered, click here to start your submission. Manuscripts can be submitted now or up until the deadline. All papers will go through peer-review process. Accepted papers will be published in the journal (as soon as accepted) and meanwhile listed together on the special issue website. Research articles, reviews as well as short communications are preferred. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office to announce on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts will be thoroughly refereed through a double-blind peer-review process. Please visit the Instruction for Authors page before submitting a manuscript. The Article Processing Charge (APC) in this open access journal is 2600 USD. Submitted manuscripts should be well formatted in good English.

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