Target intelligence / Profile preview

F-box only protein 5 (FBXO5)

Target
FBXO5
Molecular classification
F-box protein family, Ubiquitin-proteasome pathway component, SCF (SKP1-Cullin-F-box) E3 ubiquitin ligase complex subunit, Cell cycle regulatory protein
01

Overview

F-box only protein 5 (FBXO5), also known as early mitotic inhibitor 1 (EMI1), is a member of the F-box protein family functioning as a substrate recognition subunit of the SCF E3 ubiquitin ligase complex. FBXO5 plays a critical role in regulating the cell cycle by inhibiting the anaphase-promoting complex/cyclosome (APC/C), thereby ensuring proper transition into S and M phases. Dysregulation and overexpression of FBXO5 are frequently observed in multiple human cancers, where it contributes to uncontrolled cell proliferation, genomic instability, and poor clinical outcomes. FBXO5 is considered a promising therapeutic target and prognostic biomarker in oncology research due to its foundational role in cell cycle control and tumorigenesis[1][2].

Other names
EMI1F-box protein 5Fbx5early mitotic inhibitor 1early fission inhibitory protein 1
02

Mechanism of action

Inhibitors (theoretical or preclinical) would act by blocking FBXO5, leading to release of APC/C inhibition, altered cell cycle progression, and possibly genomic stabilization[2]. FBXO5 indirectly modulates sensitivity to PARP inhibitors through regulation of RAD51 degradation and homologous recombination in breast cancer[2].

03

Biological functions

Cell cycle regulationUbiquitin-dependent protein degradationInhibition of the anaphase-promoting complex/cyclosome (APC/C)Genomic stability maintenanceRegulation of cell proliferationRegulation of apoptosis
04

Disease associations

CancerGenomic instability disorders
05

Safety considerations

Targeting FBXO5 may disrupt normal cell cycle regulation, causing cytotoxicity in proliferating normal tissues[2].Genomic instability and off-target effects in cell cycle processes are possible.
06

Interacting drugs

No specific approved drugs or chemical inhibitors directly targeting FBXO5 in clinical use identified in current literature; however, FBXO5 is indirectly implicated in response to cell cycle and DNA damage-related therapies such as poly(ADP-ribose) polymerase inhibitors (PARPis) and possibly others within oncology research contexts[2].
07

Biomarkers

FBXO5 overexpression is associated with poor prognosis, high tumor grade, lymph node metastasis, and adverse outcomes in multiple cancer types (especially breast, ovarian, cervical, and head and neck cancer), and thus can serve as a prognostic biomarker[2].

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